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| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 陳小梨 | zh_TW |
| dc.contributor.advisor | Show-li Chen | en |
| dc.contributor.author | 黃健庭 | zh_TW |
| dc.contributor.author | Chien-Ting Huang | en |
| dc.date.accessioned | 2025-09-22T16:10:19Z | - |
| dc.date.available | 2025-09-23 | - |
| dc.date.copyright | 2025-09-22 | - |
| dc.date.issued | 2025 | - |
| dc.date.submitted | 2025-07-31 | - |
| dc.identifier.citation | S.-W. Chang, Y.-P. Tsao, C.-Y. Lin, and S.-L. Chen, "NRIP, a Novel Calmodulin Binding Protein, Activates Calcineurin To Dephosphorylate Human Papillomavirus E2 Protein," Journal of Virology, vol. 85, no. 13, pp. 6750-6763, 2011, doi: 10.1128/jvi.02453-10.
T.-C. Tsai, Y.-L. Lee, W.-C. Hsiao, Y.-P. Tsao, and S.-L. Chen, "NRIP, a Novel Nuclear Receptor Interaction Protein, Enhances the Transcriptional Activity of Nuclear Receptors*," Journal of Biological Chemistry, vol. 280, no. 20, pp. 20000-20009, 2005/05/20/ 2005, doi: https://doi.org/10.1074/jbc.M412169200. H.-H. Chen et al., "NRIP is newly identified as a Z-disc protein, activating calmodulin signaling for skeletal muscle contraction and regeneration," Journal of Cell Science, vol. 128, no. 22, pp. 4196-4209, 2015, doi: 10.1242/jcs.174441. P.-H. Chen, Y.-P. Tsao, C.-C. Wang, and S.-L. Chen, "Nuclear receptor interaction protein, a coactivator of androgen receptors (AR), is regulated by AR and Sp1 to feed forward and activate its own gene expression through AR protein stability," Nucleic Acids Research, vol. 36, no. 1, pp. 51-66, 2007, doi: 10.1093/nar/gkm942. S. W. Chang, P. Y. Lu, J. H. Guo, T. C. Tsai, Y. P. Tsao, and S. L. Chen, "NRIP enhances HPV gene expression via interaction with either GR or E2," (in eng), Virology, vol. 423, no. 1, pp. 38-48, Feb 5 2012, doi: 10.1016/j.virol.2011.11.015. K.-C. Yang et al., "Deficiency of nuclear receptor interaction protein leads to cardiomyopathy by disrupting sarcomere structure and mitochondrial respiration," Journal of Molecular and Cellular Cardiology, vol. 137, pp. 9-24, 2019. L. K. Tsai et al., "Autoantibody of NRIP, a novel AChR‐interacting protein, plays a detrimental role in myasthenia gravis," Journal of Cachexia, Sarcopenia and Muscle, vol. 12, no. 3, pp. 665-676, 2021. B. Khalil, K. Marwaha, and P. C. Bollu, "Physiology, Neuromuscular Junction," in StatPearls. Treasure Island (FL): StatPearls Publishing Copyright © 2025, StatPearls Publishing LLC., 2025. P. M. Rodríguez Cruz, J. Cossins, D. Beeson, and A. Vincent, "The Neuromuscular Junction in Health and Disease: Molecular Mechanisms Governing Synaptic Formation and Homeostasis," (in eng), Front Mol Neurosci, vol. 13, p. 610964, 2020, doi: 10.3389/fnmol.2020.610964. E. Ferraro, F. Molinari, and L. Berghella, "Molecular control of neuromuscular junction development," (in eng), J Cachexia Sarcopenia Muscle, vol. 3, no. 1, pp. 13-23, Mar 2012, doi: 10.1007/s13539-011-0041-7. M. Naguib, P. Flood, J. J. McArdle, and H. R. Brenner, "Advances in neurobiology of the neuromuscular junction: implications for the anesthesiologist," (in eng), Anesthesiology, vol. 96, no. 1, pp. 202-31, Jan 2002, doi: 10.1097/00000542-200201000-00035. H. Cetin, D. Beeson, A. Vincent, and R. Webster, "The Structure, Function, and Physiology of the Fetal and Adult Acetylcholine Receptor in Muscle," (in eng), Front Mol Neurosci, vol. 13, p. 581097, 2020, doi: 10.3389/fnmol.2020.581097. N. Unwin, "Nicotinic acetylcholine receptor and the structural basis of neuromuscular transmission: insights from Torpedo postsynaptic membranes," (in eng), Q Rev Biophys, vol. 46, no. 4, pp. 283-322, Nov 2013, doi: 10.1017/s0033583513000061. S. Evans, D. Goldman, S. Heinemann, and J. Patrick, "Muscle acetylcholine receptor biosynthesis. Regulation by transcript availability," (in eng), J Biol Chem, vol. 262, no. 10, pp. 4911-6, Apr 5 1987. M. A. Ruegg and J. L. Bixby, "Agrin orchestrates synaptic differentiation at the vertebrate neuromuscular junction," (in eng), Trends Neurosci, vol. 21, no. 1, pp. 22-7, Jan 1998, doi: 10.1016/s0166-2236(97)01154-5. B. Zhang, S. Luo, Q. Wang, T. Suzuki, W. C. Xiong, and L. Mei, "LRP4 serves as a coreceptor of agrin," (in eng), Neuron, vol. 60, no. 2, pp. 285-97, Oct 23 2008, doi: 10.1016/j.neuron.2008.10.006. N. Kim et al., "Lrp4 is a receptor for Agrin and forms a complex with MuSK," (in eng), Cell, vol. 135, no. 2, pp. 334-42, Oct 17 2008, doi: 10.1016/j.cell.2008.10.002. Y. Zong and R. Jin, "Structural mechanisms of the agrin-LRP4-MuSK signaling pathway in neuromuscular junction differentiation," (in eng), Cell Mol Life Sci, vol. 70, no. 17, pp. 3077-88, Sep 2013, doi: 10.1007/s00018-012-1209-9. [19] K. Okada et al., "The muscle protein Dok-7 is essential for neuromuscular synaptogenesis," (in eng), Science, vol. 312, no. 5781, pp. 1802-5, Jun 23 2006, doi: 10.1126/science.1127142. E. Bergamin, P. T. Hallock, S. J. Burden, and S. R. Hubbard, "The cytoplasmic adaptor protein Dok7 activates the receptor tyrosine kinase MuSK via dimerization," (in eng), Mol Cell, vol. 39, no. 1, pp. 100-9, Jul 9 2010, doi: 10.1016/j.molcel.2010.06.007. A. Buyan, A. C. Kalli, and M. S. Sansom, "Multiscale Simulations Suggest a Mechanism for the Association of the Dok7 PH Domain with PIP-Containing Membranes," (in eng), PLoS Comput Biol, vol. 12, no. 7, p. e1005028, Jul 2016, doi: 10.1371/journal.pcbi.1005028. B. Z. Camurdanoglu, C. Hrovat, G. Dürnberger, M. Madalinski, K. Mechtler, and R. Herbst, "MuSK Kinase Activity is Modulated By A Serine Phosphorylation Site in The Kinase Loop," (in eng), Sci Rep, vol. 6, p. 33583, Sep 26 2016, doi: 10.1038/srep33583. J. H. Till et al., "Crystal structure of the MuSK tyrosine kinase: insights into receptor autoregulation," (in eng), Structure, vol. 10, no. 9, pp. 1187-96, Sep 2002, doi: 10.1016/s0969-2126(02)00814-6. H. Zhou, D. J. Glass, G. D. Yancopoulos, and J. R. Sanes, "Distinct domains of MuSK mediate its abilities to induce and to associate with postsynaptic specializations," (in eng), J Cell Biol, vol. 146, no. 5, pp. 1133-46, Sep 6 1999, doi: 10.1083/jcb.146.5.1133. H. Darabid, A. P. Perez-Gonzalez, and R. Robitaille, "Neuromuscular synaptogenesis: coordinating partners with multiple functions," (in eng), Nat Rev Neurosci, vol. 15, no. 11, pp. 703-18, Nov 2014. T. T. Kummer, T. Misgeld, and J. R. Sanes, "Assembly of the postsynaptic membrane at the neuromuscular junction: paradigm lost," (in eng), Curr Opin Neurobiol, vol. 16, no. 1, pp. 74-82, Feb 2006, doi: 10.1016/j.conb.2005.12.003. L. Shi, A. K. Fu, and N. Y. Ip, "Molecular mechanisms underlying maturation and maintenance of the vertebrate neuromuscular junction," (in eng), Trends Neurosci, vol. 35, no. 7, pp. 441-53, Jul 2012, doi: 10.1016/j.tins.2012.04.005. L. A. Tintignac, H.-R. Brenner, and M. A. Rüegg, "Mechanisms Regulating Neuromuscular Junction Development and Function and Causes of Muscle Wasting," Physiological Reviews, vol. 95, no. 3, pp. 809-852, 2015, doi: 10.1152/physrev.00033.2014. H. Wu, W. C. Xiong, and L. Mei, "To build a synapse: signaling pathways in neuromuscular junction assembly," (in eng), Development, vol. 137, no. 7, pp. 1017-33, Apr 2010, doi: 10.1242/dev.038711. E. Mihailovska et al., "Neuromuscular synapse integrity requires linkage of acetylcholine receptors to postsynaptic intermediate filament networks via rapsyn-plectin 1f complexes," (in eng), Mol Biol Cell, vol. 25, no. 25, pp. 4130-49, Dec 15 2014, doi: 10.1091/mbc.E14-06-1174. L. Li et al., "Enzymatic Activity of the Scaffold Protein Rapsyn for Synapse Formation," (in eng), Neuron, vol. 92, no. 5, pp. 1007-1019, Dec 7 2016, doi: 10.1016/j.neuron.2016.10.023. F. Chen, Y. Liu, Y. Sugiura, P. D. Allen, R. G. Gregg, and W. Lin, "Neuromuscular synaptic patterning requires the function of skeletal muscle dihydropyridine receptors," (in eng), Nat Neurosci, vol. 14, no. 5, pp. 570-7, May 2011, doi: 10.1038/nn.2792. F. Chen et al., "Rapsyn interaction with calpain stabilizes AChR clusters at the neuromuscular junction," (in eng), Neuron, vol. 55, no. 2, pp. 247-60, Jul 19 2007, doi: 10.1016/j.neuron.2007.06.031. P. Mohseni et al., "Nestin is not essential for development of the CNS but required for dispersion of acetylcholine receptor clusters at the area of neuromuscular junctions," (in eng), J Neurosci, vol. 31, no. 32, pp. 11547-52, Aug 10 2011, doi: 10.1523/jneurosci.4396-10.2011. L. Shi et al., "Ephexin1 is required for structural maturation and neurotransmission at the neuromuscular junction," (in eng), Neuron, vol. 65, no. 2, pp. 204-16, Jan 28 2010, doi: 10.1016/j.neuron.2010.01.012. H. Tang et al., "CaM kinase II-dependent phosphorylation of myogenin contributes to activity-dependent suppression of nAChR gene expression in developing rat myotubes," (in eng), Cell Signal, vol. 16, no. 5, pp. 551-63, May 2004, doi: 10.1016/j.cellsig.2003.09.006. J. Y. Wang et al., "Caspase-3 cleavage of dishevelled induces elimination of postsynaptic structures," (in eng), Dev Cell, vol. 28, no. 6, pp. 670-84, Mar 31 2014, doi: 10.1016/j.devcel.2014.02.009. J. Yang, B. Dominguez, F. de Winter, T. W. Gould, J. E. Eriksson, and K. F. Lee, "Nestin negatively regulates postsynaptic differentiation of the neuromuscular synapse," (in eng), Nat Neurosci, vol. 14, no. 3, pp. 324-30, Mar 2011, doi: 10.1038/nn.2747. X. M. Li et al., "Retrograde regulation of motoneuron differentiation by muscle beta-catenin," (in eng), Nat Neurosci, vol. 11, no. 3, pp. 262-8, Mar 2008, doi: 10.1038/nn2053. M. Wong and L. J. Martin, "Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic mice," (in eng), Hum Mol Genet, vol. 19, no. 11, pp. 2284-302, Jun 1 2010, doi: 10.1093/hmg/ddq106. H. Wu et al., "Distinct roles of muscle and motoneuron LRP4 in neuromuscular junction formation," Neuron, vol. 75, no. 1, pp. 94-107, 2012. H. H. Chen et al., "Muscle-restricted nuclear receptor interaction protein knockout causes motor neuron degeneration through down-regulation of myogenin at the neuromuscular junction," (in eng), J Cachexia Sarcopenia Muscle, vol. 9, no. 4, pp. 771-785, Aug 2018, doi: 10.1002/jcsm.12299. 韓雅如, "NRIP藉由調控F-actin參與肌細胞融合," 碩士, 微生物學研究所, 國立臺灣大學, 2019年, 2019. C. J. Padilla et al., "Profiling age-related muscle weakness and wasting: neuromuscular junction transmission as a driver of age-related physical decline," (in eng), Geroscience, vol. 43, no. 3, pp. 1265-1281, Jun 2021, doi: 10.1007/s11357-021-00369-3. J. C. Rivera, G. Glebus, and M. Cho, "Disability following combat-sustained nerve injury of the upper limb," The bone & joint journal, vol. 96, no. 2, pp. 254-258, 2014. C. A. Taylor, D. Braza, J. B. Rice, and T. Dillingham, "The incidence of peripheral nerve injury in extremity trauma," American journal of physical medicine & rehabilitation, vol. 87, no. 5, pp. 381-385, 2008. E. D. Kosco, H. Jing, P. Chen, W. C. Xiong, I. S. Samuels, and L. Mei, "DOK7 Promotes NMJ Regeneration After Nerve Injury," (in eng), Mol Neurobiol, vol. 60, no. 3, pp. 1453-1464, Mar 2023, doi: 10.1007/s12035-022-03143-4. A. Alhindi et al., "Terminal Schwann cells at the human neuromuscular junction," Brain Communications, vol. 3, no. 2, p. fcab081, 2021, doi: 10.1093/braincomms/fcab081. T. Yamaguchi, K. Kouzaki, K. Sasaki, and K. Nakazato, "Alterations in neuromuscular junction morphology with ageing and endurance training modulate neuromuscular transmission and myofibre composition," (in eng), J Physiol, vol. 603, no. 1, pp. 107-125, Jan 2025, doi: 10.1113/jp285143. M. Fujitani, A. M. M. Tarif, and Y. Otani, "Regeneration mechanisms and therapeutic strategies for neuromuscular junctions in aging and diseases," (in eng), Neural Regen Res, vol. 20, no. 1, pp. 193-194, Jan 1 2025, doi: 10.4103/nrr.Nrr-d-23-02055. X. Li, Y. Xu, J. X. Si, F. Gu, and Y. Y. Ma, "Role of Agrin in tissue repair and regeneration: From mechanisms to therapeutic opportunities (Review)," (in eng), Int J Mol Med, vol. 54, no. 5, Nov 2024, doi: 10.3892/ijmm.2024.5422. S. Stanga, M. Boido, and P. Kienlen-Campard, "How to Build and to Protect the Neuromuscular Junction: The Role of the Glial Cell Line-Derived Neurotrophic Factor," (in eng), Int J Mol Sci, vol. 22, no. 1, Dec 24 2020, doi: 10.3390/ijms22010136. E. Molotsky, Y. Liu, A. P. Lieberman, and D. E. Merry, "Neuromuscular junction pathology is correlated with differential motor unit vulnerability in spinal and bulbar muscular atrophy," (in eng), Acta Neuropathol Commun, vol. 10, no. 1, p. 97, Jul 5 2022, doi: 10.1186/s40478-022-01402-y. D. Borgia et al., "Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients," (in eng), Hum Mol Genet, vol. 26, no. 6, pp. 1087-1103, Mar 15 2017, doi: 10.1093/hmg/ddx019. A. Rocchi et al., "Glycolytic-to-oxidative fiber-type switch and mTOR signaling activation are early-onset features of SBMA muscle modified by high-fat diet," (in eng), Acta Neuropathol, vol. 132, no. 1, pp. 127-44, Jul 2016, doi: 10.1007/s00401-016-1550-4. A. Schenone et al., "Basic Pathological Mechanisms in Peripheral Nerve Diseases," International Journal of Molecular Sciences, vol. 26, no. 7, p. 3377, 2025. T. Tezuka et al., "The MuSK activator agrin has a separate role essential for postnatal maintenance of neuromuscular synapses," Proceedings of the National Academy of Sciences, vol. 111, no. 46, pp. 16556-16561, 2014, doi: doi:10.1073/pnas.1408409111. A. Barik et al., "LRP4 is critical for neuromuscular junction maintenance," (in eng), J Neurosci, vol. 34, no. 42, pp. 13892-905, Oct 15 2014, doi: 10.1523/jneurosci.1733-14.2014. T. Eguchi, T. Tezuka, S. Miyoshi, and Y. Yamanashi, "Postnatal knockdown of dok-7 gene expression in mice causes structural defects in neuromuscular synapses and myasthenic pathology," Genes to Cells, vol. 21, no. 6, pp. 670-676, 2016, doi: https://doi.org/10.1111/gtc.12370. R. Ueta et al., "DOK7 Gene Therapy Enhances Neuromuscular Junction Innervation and Motor Function in Aged Mice," (in eng), iScience, vol. 23, no. 8, p. 101385, Aug 21 2020, doi: 10.1016/j.isci.2020.101385. A. Inoue et al., "Dok-7 Activates the Muscle Receptor Kinase MuSK and Shapes Synapse Formation," Science Signaling, vol. 2, no. 59, pp. ra7-ra7, 2009, doi: doi:10.1126/scisignal.2000113. B. Vannucci et al., "What is Normal? Neuromuscular junction reinnervation after nerve injury," Muscle & nerve, vol. 60, no. 5, pp. 604-612, 2019. T. Gordon, "Peripheral Nerve Regeneration and Muscle Reinnervation," International Journal of Molecular Sciences, vol. 21, no. 22, p. 8652, 2020. [Online]. Available: https://www.mdpi.com/1422-0067/21/22/8652. X. Huang, J. Jiang, and J. Xu, "Denervation-related neuromuscular junction changes: From degeneration to regeneration," Frontiers in Molecular Neuroscience, vol. 14, p. 810919, 2022. E. D. Kosco, H. Jing, P. Chen, W.-C. Xiong, I. S. Samuels, and L. Mei, "DOK7 promotes NMJ regeneration after nerve injury," Molecular Neurobiology, vol. 60, no. 3, pp. 1453-1464, 2023. T. W. Gould and H. Enomoto, "Neurotrophic modulation of motor neuron development," The Neuroscientist, vol. 15, no. 1, pp. 105-116, 2009. C. E. Henderson et al., "GDNF: a potent survival factor for motoneurons present in peripheral nerve and muscle," Science, vol. 266, no. 5187, pp. 1062-1064, 1994. H. B. Rind, R. Butowt, and C. S. von Bartheld, "Synaptic targeting of retrogradely transported trophic factors in motoneurons: comparison of glial cell line-derived neurotrophic factor, brain-derived neurotrophic factor, and cardiotrophin-1 with tetanus toxin," Journal of Neuroscience, vol. 25, no. 3, pp. 539-549, 2005. M. Takahashi, "The GDNF/RET signaling pathway and human diseases," Cytokine & growth factor reviews, vol. 12, no. 4, pp. 361-373, 2001. T. W. Gould, S. Yonemura, R. W. Oppenheim, S. Ohmori, and H. Enomoto, "The neurotrophic effects of glial cell line-derived neurotrophic factor on spinal motoneurons are restricted to fusimotor subtypes," Journal of Neuroscience, vol. 28, no. 9, pp. 2131-2146, 2008. J. Whitehead, C. Keller-Peck, J. Kucera, and W. G. Tourtellotte, "Glial cell-line derived neurotrophic factor-dependent fusimotor neuron survival during development," Mechanisms of development, vol. 122, no. 1, pp. 27-41, 2005. N. Stifani, "Motor neurons and the generation of spinal motor neuron diversity," Frontiers in cellular neuroscience, vol. 8, p. 293, 2014. S. Lefebvre et al., "Identification and characterization of a spinal muscular atrophy-determining gene," Cell, vol. 80, no. 1, pp. 155-165, 1995. P. McAndrew et al., "Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number," The American Journal of Human Genetics, vol. 60, no. 6, pp. 1411-1422, 1997. B. Wirth, "An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA)," Human mutation, vol. 15, no. 3, pp. 228-237, 2000. T. W. Prior, "Spinal muscular atrophy diagnostics," Journal of child neurology, vol. 22, no. 8, pp. 952-956, 2007. C. L. Lorson, E. Hahnen, E. J. Androphy, and B. Wirth, "A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy," Proceedings of the National Academy of Sciences, vol. 96, no. 11, pp. 6307-6311, 1999. U. R. Monani et al., "A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2," Human molecular genetics, vol. 8, no. 7, pp. 1177-1183, 1999. B. Schrank et al., "Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos," Proceedings of the National Academy of Sciences, vol. 94, no. 18, pp. 9920-9925, 1997. A. Broccolini, W. K. Engel, R. B. Alvarez, and V. Askanas, "Paired helical filaments of inclusion-body myositis muscle contain RNA and survival motor neuron protein," The American journal of pathology, vol. 156, no. 4, pp. 1151-1155, 2000. T. Achsel, S. Barabino, M. Cozzolino, and M. T. Carrì, "The intriguing case of motor neuron disease: ALS and SMA come closer," Biochemical Society transactions, vol. 41, no. 6, pp. 1593-1597, 2013. M. Cucchiarini, H. Madry, and E. F. Terwilliger, "Enhanced expression of the central survival of motor neuron (SMN) protein during the pathogenesis of osteoarthritis," Journal of Cellular and Molecular Medicine, vol. 18, no. 1, pp. 115-124, 2014. M. D. Howell, N. N. Singh, and R. N. Singh, "Advances in therapeutic development for spinal muscular atrophy," Future medicinal chemistry, vol. 6, no. 9, pp. 1081-1099, 2014. T. M. Wishart et al., "Dysregulation of ubiquitin homeostasis and β-catenin signaling promote spinal muscular atrophy," The Journal of clinical investigation, vol. 124, no. 4, pp. 1821-1834, 2014. N. K. Genabai, S. Ahmad, Z. Zhang, X. Jiang, C. A. Gabaldon, and L. Gangwani, "Genetic inhibition of JNK3 ameliorates spinal muscular atrophy," Human Molecular Genetics, vol. 24, no. 24, pp. 6986-7004, 2015. T. Giesemann et al., "A role for polyproline motifs in the spinal muscular atrophy protein SMN: profilins bind to and colocalize with SMN in nuclear gems," Journal of Biological Chemistry, vol. 274, no. 53, pp. 37908-37914, 1999. V. Delanote, J. Vandekerckhove, and J. Gettemans, "Plastins: versatile modulators of actin organization in (patho) physiological cellular processes," Acta Pharmacologica Sinica, vol. 26, no. 7, pp. 769-779, 2005. A. Giganti et al., "Actin-filament cross-linking protein T-plastin increases Arp2/3-mediated actin-based movement," Journal of cell science, vol. 118, no. 6, pp. 1255-1265, 2005. G. E. Oprea et al., "Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy," Science, vol. 320, no. 5875, pp. 524-527, 2008. M. Bowerman, A. Beauvais, C. L. Anderson, and R. Kothary, "Rho-kinase inactivation prolongs survival of an intermediate SMA mouse model," Human molecular genetics, vol. 19, no. 8, pp. 1468-1478, 2010. A. Nölle et al., "The spinal muscular atrophy disease protein SMN is linked to the Rho-kinase pathway via profilin," Human molecular genetics, vol. 20, no. 24, pp. 4865-4878, 2011. M. Bowerman, L. M. Murray, J. G. Boyer, C. L. Anderson, and R. Kothary, "Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy," BMC medicine, vol. 10, pp. 1-14, 2012. L. Heesen et al., "Plastin 3 is upregulated in iPSC-derived motoneurons from asymptomatic SMN1-deleted individuals," Cellular and molecular life sciences, vol. 73, pp. 2089-2104, 2016. M. Bowerman, D. Shafey, and R. Kothary, "Smn depletion alters profilin II expression and leads to upregulation of the RhoA/ROCK pathway and defects in neuronal integrity," Journal of molecular neuroscience, vol. 32, pp. 120-131, 2007. M. Bowerman, C. L. Anderson, A. Beauvais, P. P. Boyl, W. Witke, and R. Kothary, "SMN, profilin IIa and plastin 3: a link between the deregulation of actin dynamics and SMA pathogenesis," Molecular and Cellular Neuroscience, vol. 42, no. 1, pp. 66-74, 2009. B. Ackermann et al., "Plastin 3 ameliorates spinal muscular atrophy via delayed axon pruning and improves neuromuscular junction functionality," Human molecular genetics, vol. 22, no. 7, pp. 1328-1347, 2013. G. J. Doherty and H. T. McMahon, "Mechanisms of endocytosis," Annual review of biochemistry, vol. 78, no. 1, pp. 857-902, 2009. Y. Morozumi, Y. Takizawa, M. Takaku, and H. Kurumizaka, "Human PSF binds to RAD51 and modulates its homologous-pairing and strand-exchange activities," Nucleic acids research, vol. 37, no. 13, pp. 4296-4307, 2009. Y. Takizawa et al., "GEMIN2 promotes accumulation of RAD51 at double-strand breaks in homologous recombination," Nucleic acids research, vol. 38, no. 15, pp. 5059-5074, 2010. H.-L. Wen, Y.-T. Lin, C.-H. Ting, S. Lin-Chao, H. Li, and H. M. Hsieh-Li, "Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy," Human molecular genetics, vol. 19, no. 9, pp. 1766-1778, 2010. K. T. Chan, D. W. Roadcap, N. Holoweckyj, and J. E. Bear, "Coronin 1C harbours a second actin-binding site that confers co-operative binding to F-actin," Biochemical Journal, vol. 444, no. 1, pp. 89-96, 2012. R. E. Moses and B. W. O'Malley, "DNA transcription and repair: a confluence," Journal of Biological Chemistry, vol. 287, no. 28, pp. 23266-23270, 2012. M. Sabra, P. Texier, J. El Maalouf, and P. Lomonte, "The Tudor protein survival motor neuron (SMN) is a chromatin-binding protein that interacts with methylated lysine 79 of histone H3," Journal of cell science, vol. 126, no. 16, pp. 3664-3677, 2013. S. Tisdale et al., "SMN is essential for the biogenesis of U7 small nuclear ribonucleoprotein and 3′-end formation of histone mRNAs," Cell reports, vol. 5, no. 5, pp. 1187-1195, 2013. M. Dimitriadi et al., "Decreased function of survival motor neuron protein impairs endocytic pathways," Proceedings of the National Academy of Sciences, vol. 113, no. 30, pp. E4377-E4386, 2016. S. Hosseinibarkooie et al., "The power of human protective modifiers: PLS3 and CORO1C unravel impaired endocytosis in spinal muscular atrophy and rescue SMA phenotype," The American Journal of Human Genetics, vol. 99, no. 3, pp. 647-665, 2016. E. W. Ottesen, M. D. Howell, N. N. Singh, J. Seo, E. M. Whitley, and R. N. Singh, "Severe impairment of male reproductive organ development in a low SMN expressing mouse model of spinal muscular atrophy," Scientific reports, vol. 6, no. 1, p. 20193, 2016. D. Yanling Zhao et al., "SMN and symmetric arginine dimethylation of RNA polymerase II C-terminal domain control termination," Nature, vol. 529, no. 7584, pp. 48-53, 2016. P. C. Stirling and P. Hieter, "Canonical DNA repair pathways influence R-loop-driven genome instability," Journal of molecular biology, vol. 429, no. 21, pp. 3132-3138, 2017. J. M. Espinosa and B. M. Emerson, "Transcriptional regulation by p53 through intrinsic DNA/chromatin binding and site-directed cofactor recruitment," Molecular cell, vol. 8, no. 1, pp. 57-69, 2001. J. Jin, E. E. Arias, J. Chen, J. W. Harper, and J. C. Walter, "A family of diverse Cul4-Ddb1-interacting proteins includes Cdt2, which is required for S phase destruction of the replication factor Cdt1," Molecular cell, vol. 23, no. 5, pp. 709-721, 2006. H.-W. Pan, H.-Y. E. Chou, S.-H. Liu, S.-Y. Peng, C.-L. Liu, and H.-C. Hsu, "Role of L2DTL, cell Cycle-Regulated nuclear and centrosome protein, in aggressive HepatocellularCarcinoma," Cell cycle, vol. 5, no. 22, pp. 2676-2687, 2006. K. Hrecka et al., "Lentiviral Vpr usurps Cul4–DDB1 [VprBP] E3 ubiquitin ligase to modulate cell cycle," Proceedings of the National Academy of Sciences, vol. 104, no. 28, pp. 11778-11783, 2007. J. Lee and P. Zhou, "DCAFs, the missing link of the CUL4-DDB1 ubiquitin ligase," Molecular cell, vol. 26, no. 6, pp. 775-780, 2007. G. Maria Fimia et al., "Ambra1 regulates autophagy and development of the nervous system," Nature, vol. 447, no. 7148, pp. 1121-1125, 2007. T. Abbas, U. Sivaprasad, K. Terai, V. Amador, M. Pagano, and A. Dutta, "PCNA-dependent regulation of p21 ubiquitylation and degradation via the CRL4Cdt2 ubiquitin ligase complex," Genes & development, vol. 22, no. 18, pp. 2496-2506, 2008. T. Ueki et al., "Involvement of elevated expression of multiple cell-cycle regulator, DTL/RAMP (denticleless/RA-regulated nuclear matrix associated protein), in the growth of breast cancer cells," Oncogene, vol. 27, no. 43, pp. 5672-5683, 2008. J. Li et al., "Identification of retinoic acid-regulated nuclear matrix-associated protein as a novel regulator of gastric cancer," British journal of cancer, vol. 101, no. 4, pp. 691-698, 2009. F. Strappazzon et al., "Mitochondrial BCL‐2 inhibits AMBRA1‐induced autophagy," The EMBO journal, vol. 30, no. 7, pp. 1195-1208, 2011. K. Kim et al., "Vpr-binding protein antagonizes p53-mediated transcription via direct interaction with H3 tail," Molecular and cellular biology, vol. 32, no. 4, pp. 783-796, 2012. J. R. Hall, M. S. Bereman, A. I. Nepomuceno, E. A. Thompson, D. C. Muddiman, and R. C. Smart, "C/EBPα regulates CRL4cdt2-mediated degradation of p21 in response to UVB-induced DNA damage to control the G1/S checkpoint," Cell cycle, vol. 13, no. 22, pp. 3602-3610, 2014. W. Li et al., "Merlin/NF2 loss-driven tumorigenesis linked to CRL4DCAF1-mediated inhibition of the Hippo pathway kinases Lats1 and 2 in the nucleus," Cancer cell, vol. 26, no. 1, pp. 48-60, 2014. H.-H. Chen, J.-G. Chang, R.-M. Lu, T.-Y. Peng, and W.-Y. Tarn, "The RNA binding protein hnRNP Q modulates the utilization of exon 7 in the survival motor neuron 2 (SMN2) gene," Molecular and cellular biology, vol. 28, no. 22, pp. 6929-6938, 2008. Y.-C. Chen, J.-G. Chang, Y.-J. Jong, T.-Y. Liu, and C.-Y. Yuo, "High expression level of Tra2-β1 is responsible for increased SMN2 exon 7 inclusion in the testis of SMA mice," PLoS One, vol. 10, no. 3, p. e0120721, 2015. J. L. Shadrach and B. A. Pierchala, "Semaphorin3A signaling is dispensable for motor axon reinnervation of the adult neuromuscular junction," Eneuro, vol. 5, no. 3, 2018. A. V. Waller, "Experiments on the section of the glossopharyngeal and hypoglossal nerves of the frog, and observations of the alterations produced thereby in the structure of their primitive fibres," in Abstracts of the Papers Communicated to the Royal Society of London, 1851, no. 5: The Royal Society London, pp. 924-925. L. M. Davidoff, "Degeneration and Regeneration of the Nervous System. By S. Ramon Y Cajal, MD, FRS, Director of the Instituto Cajal, Madrid. Honorary Professor of Pathology in the University of Madrid. Translated and edited by Raoul M. May, Ph. D.(Harv.) D. ès Sc.(Paris). Laboratoires d'Anatomie et Histologie Comparées et de Chimie Biologique, Faculté des Sciences, Paris.(New York: Oxford University Press, American Branch, 1928, Vol. 1, pp. 396, and Vol. 2, pp. 369-769.)," American Journal of Psychiatry, vol. 86, no. 1, pp. 212-218, 1929. M. G. Burnett and E. L. Zager, "Pathophysiology of peripheral nerve injury: a brief review," Neurosurgical focus, vol. 16, no. 5, pp. 1-7, 2004. J. W. Griffin and W. J. Thompson, "Biology and pathology of nonmyelinating Schwann cells," Glia, vol. 56, no. 14, pp. 1518-1531, 2008. K. Jessen and R. Mirsky, "The repair Schwann cell and its function in regenerating nerves," The Journal of physiology, vol. 594, no. 13, pp. 3521-3531, 2016. [131] K. R. Jessen and R. Mirsky, "The success and failure of the Schwann cell response to nerve injury," Frontiers in cellular neuroscience, vol. 13, p. 33, 2019. M. Pellegatta and C. Taveggia, "The complex work of proteases and secretases in Wallerian degeneration: beyond neuregulin-1," Frontiers in cellular neuroscience, vol. 13, p. 93, 2019. A. A. Al-Majed, C. M. Neumann, T. M. Brushart, and T. Gordon, "Brief electrical stimulation promotes the speed and accuracy of motor axonal regeneration," Journal of Neuroscience, vol. 20, no. 7, pp. 2602-2608, 2000. T. M. Brushart, P. N. Hoffman, R. M. Royall, B. B. Murinson, C. Witzel, and T. Gordon, "Electrical stimulation promotes motoneuron regeneration without increasing its speed or conditioning the neuron," Journal of Neuroscience, vol. 22, no. 15, pp. 6631-6638, 2002. T. M. Brushart, R. Jari, V. Verge, C. Rohde, and T. Gordon, "Electrical stimulation restores the specificity of sensory axon regeneration," Experimental neurology, vol. 194, no. 1, pp. 221-229, 2005. A. Höke et al., "Schwann cells express motor and sensory phenotypes that regulate axon regeneration," Journal of Neuroscience, vol. 26, no. 38, pp. 9646-9655, 2006. T. M. Brushart et al., "Schwann cell phenotype is regulated by axon modality and central–peripheral location, and persists in vitro," Experimental neurology, vol. 247, pp. 272-281, 2013. T. Gordon, "Neurotrophic factor expression in denervated motor and sensory Schwann cells: relevance to specificity of peripheral nerve regeneration," Experimental neurology, vol. 254, pp. 99-108, 2014. S. Bolívar, X. Navarro, and E. Udina, "Schwann cell role in selectivity of nerve regeneration," Cells, vol. 9, no. 9, p. 2131, 2020. M. J. Gillespie, T. Gordon, and P. R. Murphy, "Reinnervation of the lateral gastrocnemius and soleus muscles in the rat by their common nerve," The Journal of Physiology, vol. 372, no. 1, pp. 485-500, 1986, doi: https://doi.org/10.1113/jphysiol.1986.sp016021. M. J. Gillespie, T. Gordon, and P. R. Murphy, "Motor units and histochemistry in rat lateral gastrocnemius and soleus muscles: evidence for dissociation of physiological and histochemical properties after reinnervation," Journal of Neurophysiology, vol. 57, no. 4, pp. 921-937, 1987, doi: 10.1152/jn.1987.57.4.921. C. Thomas, R. Stein, T. Gordon, R. Lee, and M. Elleker, "Patterns of reinnervation and motor unit recruitment in human hand muscles after complete ulnar and median nerve section and resuture," Journal of Neurology, Neurosurgery & Psychiatry, vol. 50, no. 3, pp. 259-268, 1987. T. Gordon and K. Gordon, "Nerve regeneration in the peripheral nervous system versus the central nervous system and the relevance to speech and hearing after nerve injuries," Journal of Communication Disorders, vol. 43, no. 4, pp. 274-285, 2010/07/01/ 2010, doi: https://doi.org/10.1016/j.jcomdis.2010.04.010. J. D. d. V. Alant, F. Senjaya, A. Ivanovic, J. Forden, A. Shakhbazau, and R. Midha, "The Impact of Motor Axon Misdirection and Attrition on Behavioral Deficit Following Experimental Nerve Injuries," PLOS ONE, vol. 8, no. 11, p. e82546, 2013, doi: 10.1371/journal.pone.0082546. G. C. W. de Ruiter, R. J. Spinner, J. Verhaagen, and M. J. A. Malessy, "Misdirection and guidance of regenerating axons after experimental nerve injury and repair: A review," (in English), Journal of Neurosurgery JNS, vol. 120, no. 2, pp. 493-501, 01 Feb. 2014 2014, doi: https://doi.org/10.3171/2013.8.JNS122300. C. B. Mantilla and G. C. Sieck, "Invited review: Mechanisms underlying motor unit plasticity in the respiratory system," Journal of applied physiology, vol. 94, no. 3, pp. 1230-1241, 2003. L. M. Landoni, J. R. Myles, T. L. Wells, W. P. Mayer, and T. Akay, "Cholinergic modulation of motor neurons through the C-boutons are necessary for the locomotor compensation for severe motor neuron loss during amyotrophic lateral sclerosis disease progression," Behavioural brain research, vol. 369, p. 111914, 2019. A. L. Oaklander and J. M. Brown, "Unilateral nerve injury produces bilateral loss of distal innervation," Annals of Neurology: Official Journal of the American Neurological Association and the Child Neurology Society, vol. 55, no. 5, pp. 639-644, 2004. S. W. Mitchell, "Injuries of nerves and their consequences," Archives of Neurology, vol. 22, no. 1, pp. 90-94, 1970. A. M. Aloisi, C. A. Porro, M. Cavazzuti, P. Baraldi, and G. Carli, "‘Mirror pain’in the formalin test: behavioral and 2-deoxyglucose studies," Pain, vol. 55, no. 2, pp. 267-273, 1993. Y. Imamura, H. Kawamoto, and O. Nakanishi, "Characterization of heat-hyperalgesia in an experimental trigeminal neuropathy in rats," Experimental brain research, vol. 116, pp. 97-103, 1997. M. Koltzenburg, P. D. Wall, and S. B. McMahon, "Does the right side know what the left is doing?," Trends in neurosciences, vol. 22, no. 3, pp. 122-127, 1999. P. E. Paulson, T. J. Morrow, and K. L. Casey, "Bilateral behavioral and regional cerebral blood flow changes during painful peripheral mononeuropathy in the rat," PAIN®, vol. 84, no. 2-3, pp. 233-245, 2000. K. Sluka, A. Kalra, and S. Moore, "Unilateral intramuscular injections of acidic saline produce a bilateral, long‐lasting hyperalgesia," Muscle & Nerve: Official Journal of the American Association of Electrodiagnostic Medicine, vol. 24, no. 1, pp. 37-46, 2001. L. Li, C. J. Xian, J.-H. Zhong, and X.-F. Zhou, "Effect of lumbar 5 ventral root transection on pain behaviors: a novel rat model for neuropathic pain without axotomy of primary sensory neurons," Experimental neurology, vol. 175, no. 1, pp. 23-34, 2002. R. Radhakrishnan, S. A. Moore, and K. A. Sluka, "Unilateral carrageenan injection into muscle or joint induces chronic bilateral hyperalgesia in rats," Pain, vol. 104, no. 3, pp. 567-577, 2003. N. Shenker, R. Haigh, E. Roberts, P. Mapp, N. Harris, and D. Blake, "A review of contralateral responses to a unilateral inflammatory lesion," Rheumatology, vol. 42, no. 11, pp. 1279-1286, 2003. B. H. Lee, J. Seong, U. J. Kim, R. Won, and J. Kim, "Behavioral characteristics of a mouse model of cancer pain," Yonsei medical journal, vol. 46, no. 2, pp. 252-259, 2005. Q.-L. Mao-Ying et al., "A rat model of bone cancer pain induced by intra-tibia inoculation of Walker 256 mammary gland carcinoma cells," Biochemical and biophysical research communications, vol. 345, no. 4, pp. 1292-1298, 2006. M. J. Arguis, J. Perez, G. Martínez, M. Ubre, and C. Gomar, "Contralateral neuropathic pain following a surgical model of unilateral nerve injury in rats," Regional Anesthesia & Pain Medicine, vol. 33, no. 3, pp. 211-216, 2008. Y.-E. Sun, C.-E. Lu, Y. Lei, Y. Liu, Z. Ma, and X. Gu, "Mas-related G-protein-coupled receptor c agonist bovine adrenal medulla 8-22 attenuates bone cancer pain in mice," International Journal of Clinical and Experimental Medicine, vol. 8, no. 11, p. 20178, 2015. S. Shaikh, P. Shortland, A. Lauto, M. Barton, J. W. Morley, and D. A. Mahns, "Sensory perturbations using suture and sutureless repair of transected median nerve in rats," Somatosensory & Motor Research, vol. 33, no. 1, pp. 20-28, 2016. J. Maleki, A. A. LeBel, G. J. Bennett, and R. J. Schwartzman, "Patterns of spread in complex regional pain syndrome, type I (reflex sympathetic dystrophy)," Pain, vol. 88, no. 3, pp. 259-266, 2000. C. S. Stohler, C. J. Kowalski, and J. P. Lund, "Muscle pain inhibits cutaneous touch perception," Pain, vol. 92, no. 3, pp. 327-333, 2001. J. Lei, H.-J. You, O. K. Andersen, T. Graven-Nielsen, and L. Arendt-Nielsen, "Homotopic and heterotopic variation in skin blood flow and temperature following experimental muscle pain in humans," Brain research, vol. 1232, pp. 85-93, 2008. N. Shenker, R. Haigh, P. Mapp, N. Harris, and D. Blake, "Contralateral hyperalgesia and allodynia following intradermal capsaicin injection in man," Rheumatology, vol. 47, no. 9, pp. 1417-1421, 2008. D. E. Perez, L. M. Wolford, E. Schneiderman, R. Movahed, C. Bourland, and E. P. Gutierrez, "Does unilateral temporomandibular total joint reconstruction result in contralateral joint pain and dysfunction?," Journal of Oral and Maxillofacial Surgery, vol. 74, no. 8, pp. 1539-1547, 2016. S. Younis et al., "Quantitative sensory testing in classical trigeminal neuralgia—a blinded study in patients with and without concomitant persistent pain," Pain, vol. 157, no. 7, pp. 1407-1414, 2016. S. A. Boudreau, E. N. Kamavuako, and M. S. Rathleff, "Distribution and symmetrical patellofemoral pain patterns as revealed by high-resolution 3D body mapping: a cross-sectional study," BMC musculoskeletal disorders, vol. 18, pp. 1-10, 2017. E. K. Enax-Krumova, S. Pohl, A. Westermann, and C. Maier, "Ipsilateral and contralateral sensory changes in healthy subjects after experimentally induced concomitant sensitization and hypoesthesia," BMC neurology, vol. 17, pp. 1-11, 2017. R. C. Maatman, M. U. Werner, M. R. Scheltinga, and R. M. Roumen, "Bilateral distribution of anterior cutaneous nerve entrapment syndrome (ACNES): are clinical features and outcomes comparable to unilateral ACNES?," Regional Anesthesia & Pain Medicine, vol. 44, no. 4, pp. 513-520, 2019. R. Pelletier, É. Paquette, D. Bourbonnais, J. Higgins, P. G. Harris, and M. A. Danino, "Bilateral sensory and motor as well as cognitive differences between persons with and without musculoskeletal disorders of the wrist and hand," Musculoskeletal Science and Practice, vol. 44, p. 102058, 2019. P. Masgoret, I. de Soto, Á. Caballero, J. Ríos, and C. Gomar, "Incidence of contralateral neurosensitive changes and persistent postoperative pain 6 months after mastectomy: A prospective, observational investigation," Medicine, vol. 99, no. 11, p. e19101, 2020. M. Sanders and W. Zuurmond, "Safety of unilateral and bilateral percutaneous cervical cordotomy in 80 terminally ill cancer patients," Journal of clinical oncology, vol. 13, no. 6, pp. 1509-1512, 1995. N. Higaki et al., "Usefulness of cordotomy in patients with cancer who experience bilateral pain: implications of increased pain and new pain," Neurosurgery, vol. 76, no. 3, pp. 249-257, 2015. V. Drinovac Vlah and L. Bach-Rojecky, "Mirror-Image Pain Update: ComplexInteractions Between Central and Peripheral Mechanisms," Molecular Neurobiology, vol. 61, no. 11, pp. 1-18, 2024/11/01 2024, doi: 10.1007/s12035-024-04102-x. Z. e. Seltzer, R. Dubner, and Y. Shir, "A novel behavioral model of neuropathic pain disorders produced in rats by partial sciatic nerve injury," Pain, vol. 43, no. 2, pp. 205-218, 1990. J. Chen, C. Luo, H.-L. Li, and H.-S. Chen, "Primary hyperalgesia to mechanical and heat stimuli following subcutaneous bee venom injection into the plantar surface of hindpaw in the conscious rat: a comparative study with the formalin test," Pain, vol. 83, no. 1, pp. 67-76, 1999. C.-F. Cheng et al., "Mirror-image pain is mediated by nerve growth factor produced from tumor necrosis factor alpha-activated satellite glia after peripheral nerve injury," PAIN®, vol. 155, no. 5, pp. 906-920, 2014. Z.-T. Bai, T. Liu, Z.-F. Chai, X.-Y. Pang, and Y.-H. Ji, "Rat pain-related responses induced by experimental scorpion BmK sting," European journal of pharmacology, vol. 552, no. 1-3, pp. 67-77, 2006. L. Colvin, M. Mark, and A. Duggan, "Bilaterally enhanced dorsal horn postsynaptic currents in a rat model of peripheral mononeuropathy," Neuroscience letters, vol. 207, no. 1, pp. 29-32, 1996. A. L. Oaklander, K. Romans, S. Horasek, A. Stocks, P. Hauer, and R. A. Meyer, "Unilateral postherpetic neuralgia is associated with bilateral sensory neuron damage," Annals of neurology, vol. 44, no. 5, pp. 789-795, 1998. P. Dubový, I. Klusakova, I. Svíženská, and V. Brazda, "Spatio-temporal changes of SDF1 and its CXCR4 receptor in the dorsal root ganglia following unilateral sciatic nerve injury as a model of neuropathic pain," Histochemistry and Cell Biology, vol. 133, pp. 323-337, 2010. R. Jančálek, P. Dubový, I. Svíženská, and I. Klusáková, "Bilateral changes of TNF-α and IL-10 protein in the lumbar and cervical dorsal root ganglia following a unilateral chronic constriction injury of the sciatic nerve," Journal of neuroinflammation, vol. 7, pp. 1-9, 2010. V. Brázda, I. Klusáková, I. H. Svíženská, and P. Dubový, "Dynamic response to peripheral nerve injury detected by in situ hybridization of IL-6 and its receptor mRNAs in the dorsal root ganglia is not strictly correlated with signs of neuropathic pain," Molecular pain, vol. 9, pp. 1744-8069-9-42, 2013. P. Dubový, V. Brázda, I. Klusáková, and I. Hradilová-Svíženská, "Bilateral elevation of interleukin-6 protein and mRNA in both lumbar and cervical dorsal root ganglia following unilateral chronic compression injury of the sciatic nerve," Journal of neuroinflammation, vol. 10, pp. 1-22, 2013. I. H. Svíženská, V. Brázda, I. Klusáková, and P. Dubový, "Bilateral changes of cannabinoid receptor type 2 protein and mRNA in the dorsal root ganglia of a rat neuropathic pain model," Journal of Histochemistry & Cytochemistry, vol. 61, no. 7, pp. 529-547, 2013. M. Fetell et al., "Cutaneous nerve fiber and peripheral Nav1. 7 assessment in a large cohort of patients with postherpetic neuralgia," Pain, vol. 164, no. 11, pp. 2435-2446, 202 | - |
| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/99966 | - |
| dc.description.abstract | 核受體交互蛋白(NRIP)為一多功能蛋白,於骨骼肌與脊髓中均有表現,參與神經肌肉接點(NMJ)穩定維持。肌肉來源的NRIP功能已有相關研究,但神經元來源NRIP(mnNRIP)的生理角色仍未釐清。本研究目的為探討mnNRIP對NMJ穩定與神經再生之貢獻。我們利用運動神經元專一性NRIP剔除小鼠(mnKO)模型,分析其脊髓中運動神經元形態、NMJ結構、運動行為與坐骨神經損傷後的再生狀態。結果發現,mnKO小鼠脊髓中大型膽鹼能神經元明顯減少,但其NMJ結構、肌纖維類型及運動功能與野生型無顯著差異。坐骨神經損傷後14天,mnKO與對照組皆展現類似的NMJ再生能力。值得注意的是,mnKO小鼠在未受傷對側肢體出現提早去神經化現象,顯示mnNRIP可能於壓力狀態下支持雙側NMJ的穩定性。總結而言,mnNRIP雖非維持NMJ結構及再生所必需,但可能參與運動神經元存活及傷後跨側神經反應之調控。 | zh_TW |
| dc.description.abstract | NRIP is a multifunctional protein expressed in muscle and spinal cord, implicated in neuromuscular junction (NMJ) maintenance. While muscle-derived NRIP supports NMJ stability, its motor neuron-derived counterpart (mnNRIP) is less studied. We aimed to determine the physiological function of mnNRIP in NMJ homeostasis and regeneration. By generating mnNRIP knockout (mnKO) mice, we examined motor neuron morphology, NMJ structure, behavioral performance, and regenerative capacity following sciatic nerve injury. mnKO mice exhibited reduced numbers of large spinal cholinergic neurons but displayed no significant changes in NMJ architecture, muscle fiber composition, or motor behavior. At 14 days after nerve injury, both mnKO and wild-type mice showed comparable NMJ regeneration. Unexpectedly, mnKO mice exhibited early signs of NMJ denervation in the contralateral, uninjured limb. These results indicate that mnNRIP is not essential for NMJ regeneration or structure under normal conditions but may play a role in supporting bilateral NMJ integrity under stress. Thus, mnNRIP contributes to motor neuron maintenance and may regulate trans-neural responses to injury. | en |
| dc.description.provenance | Submitted by admin ntu (admin@lib.ntu.edu.tw) on 2025-09-22T16:10:19Z No. of bitstreams: 0 | en |
| dc.description.provenance | Made available in DSpace on 2025-09-22T16:10:19Z (GMT). No. of bitstreams: 0 | en |
| dc.description.tableofcontents | 口試委員會審定書 I
致謝 II 中文摘要 IV Abstract V 目次 VI Chapter 1. Introduction 1 1.1 The nuclear receptor interaction protein (NRIP) 1 1.2 The physiology of neuromuscular junction (NMJ) 2 1.3 The development of NMJ and AChR cluster formation 3 1.4 The NRIP at the neuromuscular junction 5 1.5 The retrograde effect at the neuromuscular junction 6 1.6 The role of motor neuron-derived postsynaptic components 7 1.7 The role of NMJ components in regeneration after peripheral nerve injury 8 1.8 The aim of this study 8 Chapter 2. Materials and Methods 10 2.1 Mice 10 2.2 Mice spinal cord and muscles preparation 10 2.3 Immunofluorescent staining of motor neurons 11 2.4 Immunofluorescent staining of NMJ and muscle fibers 12 2.5 Behavioral analysis 15 2.6 Sciatic nerve crush injury 16 Chapter 3. Results 18 3.1 Reduced large cholinergic and NRIP-expressing neurons in NRIP mnKO mice 18 3.2 Comparable neuromuscular junction (NMJ) structure between WT and mnKO mice 20 3.3 Comparable muscle fiber types distribution in WT and mnKO mice. 21 3.4 Insignificant difference on motor function and behavior between WT and mnKO mice. 22 3.5 Completely Denervation After Sciatic Nerve Crush Injury 22 3.6 Comparable NMJ Regeneration Status 14 Days Post Injured 24 Chapter 4. Discussion 26 4.1 MN-NRIP is dispensable for NMJ function but involved in MN development in the spinal cord. 26 4.2 mnNRIP is dispensable for unilateral NMJ regeneration after sciatic nerve injury. 30 4.3 mnNRIP KO accelerates contralateral NMJ denervation after unilateral injury. 32 Chapter 5. Figures 35 Chapter 6. Supplementary information 44 Chapter 8. Appendix 47 Chapter 9. Reference 50 | - |
| dc.language.iso | en | - |
| dc.subject | 核受體交互蛋白(NRIP) | zh_TW |
| dc.subject | 神經肌肉接點(NMJ) | zh_TW |
| dc.subject | 背側膽鹼能神經元 | zh_TW |
| dc.subject | 坐骨神經損傷 | zh_TW |
| dc.subject | NMJ再生 | zh_TW |
| dc.subject | 去神經化 | zh_TW |
| dc.subject | 雙側神經調控 | zh_TW |
| dc.subject | Bilateral neuromuscular regulation | en |
| dc.subject | Sciatic nerve injury | en |
| dc.subject | Regeneration | en |
| dc.subject | Neurodegeneration | en |
| dc.subject | NRIP | en |
| dc.subject | NMJ | en |
| dc.subject | Motor neurons | en |
| dc.title | 運動神經元NRIP對運動神經及肌肉的影響 | zh_TW |
| dc.title | The Effect of mnNRIP on Motor Neuron and Muscle | en |
| dc.type | Thesis | - |
| dc.date.schoolyear | 113-2 | - |
| dc.description.degree | 碩士 | - |
| dc.contributor.coadvisor | 楊宏志 | zh_TW |
| dc.contributor.coadvisor | Hung-Chih Yang | en |
| dc.contributor.oralexamcommittee | 黃祥博;曹友平;陳伯翰 | zh_TW |
| dc.contributor.oralexamcommittee | Hsiang-Po Huang;Yeou-Ping Tsao;Po-Han Chen | en |
| dc.subject.keyword | 核受體交互蛋白(NRIP),神經肌肉接點(NMJ),背側膽鹼能神經元,坐骨神經損傷,NMJ再生,去神經化,雙側神經調控, | zh_TW |
| dc.subject.keyword | NRIP,NMJ,Motor neurons,Sciatic nerve injury,Regeneration,Bilateral neuromuscular regulation,Neurodegeneration, | en |
| dc.relation.page | 66 | - |
| dc.identifier.doi | 10.6342/NTU202503096 | - |
| dc.rights.note | 同意授權(限校園內公開) | - |
| dc.date.accepted | 2025-07-31 | - |
| dc.contributor.author-college | 醫學院 | - |
| dc.contributor.author-dept | 微生物學研究所 | - |
| dc.date.embargo-lift | 2027-12-31 | - |
| 顯示於系所單位: | 微生物學科所 | |
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| 檔案 | 大小 | 格式 | |
|---|---|---|---|
| ntu-113-2.pdf 未授權公開取用 | 1.94 MB | Adobe PDF | 檢視/開啟 |
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