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完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.advisor | 邱智賢(Chih-Hsien Chiu),鍾德憲(De-Shien Jong) | |
dc.contributor.author | Tai-Hsiang Tseng | en |
dc.contributor.author | 曾泰祥 | zh_TW |
dc.date.accessioned | 2021-06-15T01:19:31Z | - |
dc.date.available | 2010-08-12 | |
dc.date.copyright | 2009-08-12 | |
dc.date.issued | 2009 | |
dc.date.submitted | 2009-07-27 | |
dc.identifier.citation | 連韋雄。2000。應用小鼠萊吉氏細胞體外培養系統篩選具激性腺素活性之中藥。國立台灣大學畜產學研究所碩士論文,台北。
Bartke, A., and R. W. Steger. 1992. Seasonal changes in the function of the hypothalamic-pituitary-testicular axis in the Syrian hamster. Proc Soc Exp Biol Med 199:139-48. Bartness, T. J., J. B. Powers, M. H. Hastings, E. L. Bittman, and B. D. Goldman. 1993. The timed infusion paradigm for melatonin delivery: what has it taught us about the melatonin signal, its reception, and the photoperiodic control of seasonal responses? J Pineal Res 15:161-90. Brackmann, M., and K. Hoffmann. 1977. Pinealectomy and photoperiod influence testicular development in the Djungarian hamster. Naturwissenschaften 64:341-2. Brailoiu, G. C., S. L. Dun, M. Ohsawa, D. Yin, J. Yang, J. K. Chang, E. Brailoiu, and N. J. Dun. 2005. KiSS-1 expression and metastin-like immunoreactivity in the rat brain. J Comp Neurol 481:314-29. Canteras, N. S., R. B. Simerly, and L. W. Swanson. 1994. Organization of projections from the ventromedial nucleus of the hypothalamus: a Phaseolus vulgaris-leucoagglutinin study in the rat. J Comp Neurol 348:41-79. Castellano, J. M., M. Gaytan, J. Roa, E. Vigo, V. M. Navarro, C. Bellido, C. Dieguez, E. Aguilar, J. E. Sanchez-Criado, A. Pellicer, L. Pinilla, F. Gaytan, and M. Tena-Sempere. 2006. Expression of KiSS-1 in rat ovary: putative local regulator of ovulation? Endocrinology 147:4852-62. Clayton, P. E., and J. A. Trueman. 2000. Leptin and puberty. Arch Dis Child 83:1-4. Colledge, W. H. 2008. GPR54 and kisspeptins. Results Probl Cell Differ 46:117-43. d'Anglemont de Tassigny, X., L. A. Fagg, J. P. Dixon, K. Day, H. G. Leitch, A. G. Hendrick, D. Zahn, I. Franceschini, A. Caraty, M. B. Carlton, S. A. Aparicio, and W. H. Colledge. 2007. Hypogonadotropic hypogonadism in mice lacking a functional Kiss1 gene. Proc Natl Acad Sci U S A 104:10714-9. de Roux, N., E. Genin, J. C. Carel, F. Matsuda, J. L. Chaussain, and E. Milgrom. 2003. Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54. Proc Natl Acad Sci U S A 100:10972-6. Dhillo, W. S. 2008. Kisspeptin: a novel regulator of reproductive function. J Neuroendocrinol 20:963-70. Dhillo, W. S., O. B. Chaudhri, M. Patterson, E. L. Thompson, K. G. Murphy, M. K. Badman, B. M. McGowan, V. Amber, S. Patel, M. A. Ghatei, and S. R. Bloom. 2005. Kisspeptin-54 stimulates the hypothalamic-pituitary gonadal axis in human males. J Clin Endocrinol Metab 90:6609-15. Dhillo, W. S., P. Savage, K. G. Murphy, O. B. Chaudhri, M. Patterson, G. M. Nijher, V. M. Foggo, G. S. Dancey, H. Mitchell, M. J. Seckl, M. A. Ghatei, and S. R. Bloom. 2006. Plasma kisspeptin is raised in patients with gestational trophoblastic neoplasia and falls during treatment. Am J Physiol Endocrinol Metab 291:E878-84. Dungan, H. M., D. K. Clifton, and R. A. Steiner. 2006. Minireview: kisspeptin neurons as central processors in the regulation of gonadotropin-releasing hormone secretion. Endocrinology 147:1154-8. Dungan, H. M., M. L. Gottsch, H. Zeng, A. Gragerov, J. E. Bergmann, D. K. Vassilatis, D. K. Clifton, and R. A. Steiner. 2007. The role of kisspeptin-GPR54 signaling in the tonic regulation and surge release of gonadotropin-releasing hormone/luteinizing hormone. J Neurosci 27:12088-95. Funes, S., J. A. Hedrick, G. Vassileva, L. Markowitz, S. Abbondanzo, A. Golovko, S. Yang, F. J. Monsma, and E. L. Gustafson. 2003. The KiSS-1 receptor GPR54 is essential for the development of the murine reproductive system. Biochem Biophys Res Commun 312:1357-63. Gaston, S., and M. Menaker. 1967. Photoperiodic control of hamster testis. Science 158:925-8. Gaytan, F., M. Gaytan, J. M. Castellano, M. Romero, J. Roa, B. Aparicio, N. Garrido, J. E. Sanchez-Criado, R. P. Millar, A. Pellicer, H. M. Fraser, and M. Tena-Sempere. 2009. KiSS-1 in the mammalian ovary: distribution of kisspeptin in human and marmoset and alterations in KiSS-1 mRNA levels in a rat model of ovulatory dysfunction. Am J Physiol Endocrinol Metab 296:E520-31. Goldman, B. D. 2001. Mammalian photoperiodic system: formal properties and neuroendocrine mechanisms of photoperiodic time measurement. J Biol Rhythms 16:283-301. Gottsch, M. L., D. K. Clifton, and R. A. Steiner. 2009. From KISS1 to kisspeptins: An historical perspective and suggested nomenclature. Peptides 30:4-9. Gottsch, M. L., M. J. Cunningham, J. T. Smith, S. M. Popa, B. V. Acohido, W. F. Crowley, S. Seminara, D. K. Clifton, and R. A. Steiner. 2004. A role for kisspeptins in the regulation of gonadotropin secretion in the mouse. Endocrinology 145:4073-7. Gu, G. B., and R. B. Simerly. 1997. Projections of the sexually dimorphic anteroventral periventricular nucleus in the female rat. J Comp Neurol 384:142-64. Hagihara, K., S. Hirata, T. Osada, M. Hirai, and J. Kato. 1992. Distribution of cells containing progesterone receptor mRNA in the female rat di- and telencephalon: an in situ hybridization study. Brain Res Mol Brain Res 14:239-49. Harms, J. F., D. R. Welch, and M. E. Miele. 2003. KISS1 metastasis suppression and emergent pathways. Clin Exp Metastasis 20:11-8. Herbison, A. E. 1998. Multimodal influence of estrogen upon gonadotropin-releasing hormone neurons. Endocr Rev 19:302-30. Hoffman, R. A., and R. J. Reiter. 1965. Pineal Gland: Influence on Gonads of Male Hamsters. Science 148:1609-11. Horikoshi, Y., H. Matsumoto, Y. Takatsu, T. Ohtaki, C. Kitada, S. Usuki, and M. Fujino. 2003. Dramatic elevation of plasma metastin concentrations in human pregnancy: metastin as a novel placenta-derived hormone in humans. J Clin Endocrinol Metab 88:914-9. Hu, W. N., R. N. Band, and W. J. Kopachik. 1991. Virulence-related protein synthesis in Naegleria fowleri. Infect Immun 59:4278-82. Irwig, M. S., G. S. Fraley, J. T. Smith, B. V. Acohido, S. M. Popa, M. J. Cunningham, M. L. Gottsch, D. K. Clifton, and R. A. Steiner. 2004. Kisspeptin activation of gonadotropin releasing hormone neurons and regulation of KiSS-1 mRNA in the male rat. Neuroendocrinology 80:264-72. Kinoshita, M., H. Tsukamura, S. Adachi, H. Matsui, Y. Uenoyama, K. Iwata, S. Yamada, K. Inoue, T. Ohtaki, H. Matsumoto, and K. Maeda. 2005. Involvement of central metastin in the regulation of preovulatory luteinizing hormone surge and estrous cyclicity in female rats. Endocrinology 146:4431-6. Kotani, M., M. Detheux, A. Vandenbogaerde, D. Communi, J. M. Vanderwinden, E. Le Poul, S. Brezillon, R. Tyldesley, N. Suarez-Huerta, F. Vandeput, C. Blanpain, S. N. Schiffmann, G. Vassart, and M. Parmentier. 2001. The metastasis suppressor gene KiSS-1 encodes kisspeptins, the natural ligands of the orphan G protein-coupled receptor GPR54. J Biol Chem 276:34631-6. Lapatto, R., J. C. Pallais, D. Zhang, Y. M. Chan, A. Mahan, F. Cerrato, W. W. Le, G. E. Hoffman, and S. B. Seminara. 2007. Kiss1-/- mice exhibit more variable hypogonadism than Gpr54-/- mice. Endocrinology 148:4927-36. Lee, D. K., T. Nguyen, G. P. O'Neill, R. Cheng, Y. Liu, A. D. Howard, N. Coulombe, C. P. Tan, A. T. Tang-Nguyen, S. R. George, and B. F. O'Dowd. 1999. Discovery of a receptor related to the galanin receptors. FEBS Lett 446:103-7. Lee, J. H., M. E. Miele, D. J. Hicks, K. K. Phillips, J. M. Trent, B. E. Weissman, and D. R. Welch. 1996. KiSS-1, a novel human malignant melanoma metastasis-suppressor gene. J Natl Cancer Inst 88:1731-7. Lee, J. H., and D. R. Welch. 1997a. Identification of highly expressed genes in metastasis-suppressed chromosome 6/human malignant melanoma hybrid cells using subtractive hybridization and differential display. Int J Cancer 71:1035-44. Lee, J. H., and D. R. Welch. 1997b. Suppression of metastasis in human breast carcinoma MDA-MB-435 cells after transfection with the metastasis suppressor gene, KiSS-1. Cancer Res 57:2384-7. Malpaux, B., M. Migaud, H. Tricoire, and P. Chemineau. 2001. Biology of mammalian photoperiodism and the critical role of the pineal gland and melatonin. J Biol Rhythms 16:336-47. Matsui, H., Y. Takatsu, S. Kumano, H. Matsumoto, and T. Ohtaki. 2004. Peripheral administration of metastin induces marked gonadotropin release and ovulation in the rat. Biochem Biophys Res Commun 320:383-8. Mead, G. 2007. The effects of cancer treatment on reproductive functions. Clin Med 7:544-5. Meister, B., and M. L. Hakansson. 2001. Leptin receptors in hypothalamus and circumventricular organs. Clin Exp Pharmacol Physiol 28:610-7. Messager, S., E. E. Chatzidaki, D. Ma, A. G. Hendrick, D. Zahn, J. Dixon, R. R. Thresher, I. Malinge, D. Lomet, M. B. Carlton, W. H. Colledge, A. Caraty, and S. A. Aparicio. 2005. Kisspeptin directly stimulates gonadotropin-releasing hormone release via G protein-coupled receptor 54. Proc Natl Acad Sci U S A 102:1761-6. Miele, M. E., M. D. Jewett, S. F. Goldberg, D. L. Hyatt, C. Morelli, F. Gualandi, P. Rimessi, D. J. Hicks, B. E. Weissman, G. Barbanti-Brodano, and D. R. Welch. 2000. A human melanoma metastasis-suppressor locus maps to 6q16.3-q23. Int J Cancer 86:524-8. Miele, M. E., G. Robertson, J. H. Lee, A. Coleman, C. T. McGary, P. B. Fisher, T. G. Lugo, and D. R. Welch. 1996. Metastasis suppressed, but tumorigenicity and local invasiveness unaffected, in the human melanoma cell line MelJuSo after introduction of human chromosomes 1 or 6. Mol Carcinog 15:284-99. Muir, A. I., L. Chamberlain, N. A. Elshourbagy, D. Michalovich, D. J. Moore, A. Calamari, P. G. Szekeres, H. M. Sarau, J. K. Chambers, P. Murdock, K. Steplewski, U. Shabon, J. E. Miller, S. E. Middleton, J. G. Darker, C. G. Larminie, S. Wilson, D. J. Bergsma, P. Emson, R. Faull, K. L. Philpott, and D. C. Harrison. 2001. AXOR12, a novel human G protein-coupled receptor, activated by the peptide KiSS-1. J Biol Chem 276:28969-75. Mullis, K., F. Faloona, S. Scharf, R. Saiki, G. Horn, and H. Erlich. 1986. Specific enzymatic amplification of DNA in vitro: the polymerase chain reaction. Cold Spring Harb Symp Quant Biol 51 Pt 1:263-73. Murphy, K. G. 2005. Kisspeptins: regulators of metastasis and the hypothalamic-pituitary-gonadal axis. J Neuroendocrinol 17:519-25. Navarro, V. M., J. M. Castellano, R. Fernandez-Fernandez, M. L. Barreiro, J. Roa, J. E. Sanchez-Criado, E. Aguilar, C. Dieguez, L. Pinilla, and M. Tena-Sempere. 2004. Developmental and hormonally regulated messenger ribonucleic acid expression of KiSS-1 and its putative receptor, GPR54, in rat hypothalamus and potent luteinizing hormone-releasing activity of KiSS-1 peptide. Endocrinology 145:4565-74. Navarro, V. M., J. M. Castellano, R. Fernandez-Fernandez, S. Tovar, J. Roa, A. Mayen, M. L. Barreiro, F. F. Casanueva, E. Aguilar, C. Dieguez, L. Pinilla, and M. Tena-Sempere. 2005a. Effects of KiSS-1 peptide, the natural ligand of GPR54, on follicle-stimulating hormone secretion in the rat. Endocrinology 146:1689-97. Navarro, V. M., J. M. Castellano, R. Fernandez-Fernandez, S. Tovar, J. Roa, A. Mayen, R. Nogueiras, M. J. Vazquez, M. L. Barreiro, P. Magni, E. Aguilar, C. Dieguez, L. Pinilla, and M. Tena-Sempere. 2005b. Characterization of the potent luteinizing hormone-releasing activity of KiSS-1 peptide, the natural ligand of GPR54. Endocrinology 146:156-63. Niida, A., Z. Wang, K. Tomita, S. Oishi, H. Tamamura, A. Otaka, J. M. Navenot, J. R. Broach, S. C. Peiper, and N. Fujii. 2006. Design and synthesis of downsized metastin (45-54) analogs with maintenance of high GPR54 agonistic activity. Bioorg Med Chem Lett 16:134-7. Ohtaki, T., Y. Shintani, S. Honda, H. Matsumoto, A. Hori, K. Kanehashi, Y. Terao, S. Kumano, Y. Takatsu, Y. Masuda, Y. Ishibashi, T. Watanabe, M. Asada, T. Yamada, M. Suenaga, C. Kitada, S. Usuki, T. Kurokawa, H. Onda, O. Nishimura, and M. Fujino. 2001. Metastasis suppressor gene KiSS-1 encodes peptide ligand of a G-protein-coupled receptor. Nature 411:613-7. Orsini, M. J., M. A. Klein, M. P. Beavers, P. J. Connolly, S. A. Middleton, and K. H. Mayo. 2007. Metastin (KiSS-1) mimetics identified from peptide structure-activity relationship-derived pharmacophores and directed small molecule database screening. J Med Chem 50:462-71. Pevet, P. 1988. The role of the pineal gland in the photoperiodic control of reproduction in different hamster species. Reprod Nutr Dev 28:443-58. Pitrosky, B., and P. Pevet. 1997. The photoperiodic response in Syrian hamsters depends upon a melatonin-driven rhythm of sensitivity to melatonin. Biol Signals 6:264-71. Plant, T. M., and G. R. Marshall. 2001. The functional significance of FSH in spermatogenesis and the control of its secretion in male primates. Endocr Rev 22:764-86. Plant, T. M., S. Ramaswamy, and M. J. Dipietro. 2006. Repetitive activation of hypothalamic G protein-coupled receptor 54 with intravenous pulses of kisspeptin in the juvenile monkey (Macaca mulatta) elicits a sustained train of gonadotropin-releasing hormone discharges. Endocrinology 147:1007-13. Revel, F. G., L. Ansel, P. Klosen, M. Saboureau, P. Pevet, J. D. Mikkelsen, and V. Simonneaux. 2007. Kisspeptin: a key link to seasonal breeding. Rev Endocr Metab Disord 8:57-65. Revel, F. G., M. Saboureau, M. Masson-Pevet, P. Pevet, J. D. Mikkelsen, and V. Simonneaux. 2006. Kisspeptin mediates the photoperiodic control of reproduction in hamsters. Curr Biol 16:1730-5. Ringel, M. D., E. Hardy, V. J. Bernet, H. B. Burch, F. Schuppert, K. D. Burman, and M. Saji. 2002. Metastin receptor is overexpressed in papillary thyroid cancer and activates MAP kinase in thyroid cancer cells. J Clin Endocrinol Metab 87:2399. Saitoh, Y., A. J. Silverman, and M. J. Gibson. 1991. Norepinephrine neurons in mouse locus coeruleus express c-fos protein after N-methyl-D,L-aspartic acid (NMDA) treatment: relation to LH release. Brain Res 561:11-9. Schwartz, W. J., H. O. de la Iglesia, P. Zlomanczuk, and H. Illnerova. 2001. Encoding le quattro stagioni within the mammalian brain: photoperiodic orchestration through the suprachiasmatic nucleus. J Biol Rhythms 16:302-11. Seminara, S. B., S. Messager, E. E. Chatzidaki, R. R. Thresher, J. S. Acierno, Jr., J. K. Shagoury, Y. Bo-Abbas, W. Kuohung, K. M. Schwinof, A. G. Hendrick, D. Zahn, J. Dixon, U. B. Kaiser, S. A. Slaugenhaupt, J. F. Gusella, S. O'Rahilly, M. B. Carlton, W. F. Crowley, Jr., S. A. Aparicio, and W. H. Colledge. 2003. The GPR54 gene as a regulator of puberty. N Engl J Med 349:1614-27. Shahab, M., C. Mastronardi, S. B. Seminara, W. F. Crowley, S. R. Ojeda, and T. M. Plant. 2005. Increased hypothalamic GPR54 signaling: a potential mechanism for initiation of puberty in primates. Proc Natl Acad Sci U S A 102:2129-34. Shi, C. S., and J. H. Kehrl. 2001. PYK2 links G(q)alpha and G(13)alpha signaling to NF-kappa B activation. J Biol Chem 276:31845-50. Shughrue, P. J., M. V. Lane, and I. Merchenthaler. 1997. Comparative distribution of estrogen receptor-alpha and -beta mRNA in the rat central nervous system. J Comp Neurol 388:507-25. Simerly, R. B. 1998. Organization and regulation of sexually dimorphic neuroendocrine pathways. Behav Brain Res 92:195-203. Simerly, R. B., C. Chang, M. Muramatsu, and L. W. Swanson. 1990. Distribution of androgen and estrogen receptor mRNA-containing cells in the rat brain: an in situ hybridization study. J Comp Neurol 294:76-95. Simonian, S. X., D. P. Spratt, and A. E. Herbison. 1999. Identification and characterization of estrogen receptor alpha-containing neurons projecting to the vicinity of the gonadotropin-releasing hormone perikarya in the rostral preoptic area of the rat. J Comp Neurol 411:346-58. Simonneaux, V., L. Ansel, F. G. Revel, P. Klosen, P. Pevet, and J. D. Mikkelsen. 2008. Kisspeptin and the seasonal control of reproduction in hamsters. Peptides. Simonneaux, V., and C. Ribelayga. 2003. Generation of the melatonin endocrine message in mammals: a review of the complex regulation of melatonin synthesis by norepinephrine, peptides, and other pineal transmitters. Pharmacol Rev 55:325-95. Smith, J. T., D. K. Clifton, and R. A. Steiner. 2006. Regulation of the neuroendocrine reproductive axis by kisspeptin-GPR54 signaling. Reproduction 131:623-30. Smith, J. T., M. J. Cunningham, E. F. Rissman, D. K. Clifton, and R. A. Steiner. 2005a. Regulation of Kiss1 gene expression in the brain of the female mouse. Endocrinology 146:3686-92. Smith, J. T., H. M. Dungan, E. A. Stoll, M. L. Gottsch, R. E. Braun, S. M. Eacker, D. K. Clifton, and R. A. Steiner. 2005b. Differential regulation of KiSS-1 mRNA expression by sex steroids in the brain of the male mouse. Endocrinology 146:2976-84. Strasberg, S. M., F. Dehdashti, B. A. Siegel, J. A. Drebin, and D. Linehan. 2001. Survival of patients evaluated by FDG-PET before hepatic resection for metastatic colorectal carcinoma: a prospective database study. Ann Surg 233:293-9. Tennant, J. R. 1964. Evaluation of the Trypan Blue Technique for Determination of Cell Viability. Transplantation 2:685-94. Thompson, E. L., M. Patterson, K. G. Murphy, K. L. Smith, W. S. Dhillo, J. F. Todd, M. A. Ghatei, and S. R. Bloom. 2004. Central and peripheral administration of kisspeptin-10 stimulates the hypothalamic-pituitary-gonadal axis. J Neuroendocrinol 16:850-8. Tomita, K., A. Niida, S. Oishi, H. Ohno, J. Cluzeau, J. M. Navenot, Z. X. Wang, S. C. Peiper, and N. Fujii. 2006. Structure-activity relationship study on small peptidic GPR54 agonists. Bioorg Med Chem 14:7595-603. Topaloglu, A. K., F. Reimann, M. Guclu, A. S. Yalin, L. D. Kotan, K. M. Porter, A. Serin, N. O. Mungan, J. R. Cook, M. N. Ozbek, S. Imamoglu, N. S. Akalin, B. Yuksel, S. O'Rahilly, and R. K. Semple. 2009. TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction. Nat Genet 41:354-8. Vitale, P. M., J. M. Darrow, M. J. Duncan, C. A. Shustak, and B. D. Goldman. 1985. Effects of photoperiod, pinealectomy and castration on body weight and daily torpor in Djungarian hamsters (Phodopus sungorus). J Endocrinol 106:367-75. Wagner, G. C., J. D. Johnston, I. J. Clarke, G. A. Lincoln, and D. G. Hazlerigg. 2008. Redefining the limits of day length responsiveness in a seasonal mammal. Endocrinology 149:32-9. Welch, D. R., J. E. Bisi, B. E. Miller, D. Conaway, E. A. Seftor, K. H. Yohem, L. B. Gilmore, R. E. Seftor, M. Nakajima, and M. J. Hendrix. 1991. Characterization of a highly invasive and spontaneously metastatic human malignant melanoma cell line. Int J Cancer 47:227-37. Welch, D. R., P. Chen, M. E. Miele, C. T. McGary, J. M. Bower, E. J. Stanbridge, and B. E. Weissman. 1994. Microcell-mediated transfer of chromosome 6 into metastatic human C8161 melanoma cells suppresses metastasis but does not inhibit tumorigenicity. Oncogene 9:255-62. Yan, C., H. Wang, and D. D. Boyd. 2001. KiSS-1 represses 92-kDa type IV collagenase expression by down-regulating NF-kappa B binding to the promoter as a consequence of Ikappa Balpha -induced block of p65/p50 nuclear translocation. J Biol Chem 276:1164-72. You, J., M. E. Miele, C. Dong, and D. R. Welch. 1995. Suppression of human melanoma metastasis by introduction of chromosome 6 may be partially due to inhibition of motility, but not to inhibition of invasion. Biochem Biophys Res Commun 208:476-84. | |
dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/42678 | - |
dc.description.abstract | 發身(puberty)是動物啟動生殖周期的發軔,並進入成熟生理的變化;不論雄性或雌性動物達發身年齡後,體內生殖內分泌開始運轉,此時下視丘會分泌促性腺激素釋放激素(Gonadotropin release hormone, GnRH),進而刺激腦垂腺之排卵素(LH)、濾泡激素(FSH)等激性腺素分泌,使性腺發育成熟。此為現今熟知能調控動物生殖生理機制的HPG軸(Hypothalamic-pituitary-gonad axis) 。近年來發現,人類和小鼠下視丘上GPR54 (G protein-coupled receptor 54)受體可調控GnRH神經元分泌GnRH,進而促使腦垂腺分泌LH及FSH以調控HPG軸的運作。
GPR54是一種G蛋白偶合受體,最初在1999年被發現時,並未找到其配體(ligand),故被分類為新型孤兒G蛋白偶合受體(new orphan GPCR)。直至2001年GPR54的配體kisspeptin才隨之發現。Kisspeptin 蛋白為145個胺基酸的親水性蛋白,在不同物種間Kiss1蛋白的序列都有其相似性,譬如在胜汰前的分泌序列(secretory signal sequence),中間的PEST序列及共同的磷酸化位置。KiSS-1相對應的受體為GPR54,又稱作hOT7T175或是AXOR12,是GPCR家族的成員之一。在動物組織分佈的方面,GPR54和kisspeptin兩者經常於同一位置表現,而胎盤中兩者的表現量都很高,可能參與催產功能(Horikoshi et al., 2003);此外,KiSS-1和GPR54兩者在神經系統的分佈相對廣泛,尤其是在下視丘和腦垂體。除了神經系統外,KiSS-1也在睪丸、胰臟、肝臟和小腸有表現,而GPR54則會在胰臟大量表現,另外在脾臟、淋巴結及脂肪組織中也有少量表現。 雖已知kisspeptin與GPR54表現於許多動物組織中,但科學家截至目前只對其與HPG軸之上游較為明瞭,而其他組織表現之kisspeptin與GPR54尚需更多研究證實其功能。因此,本試驗利用十二週齡之ICR小鼠,取其組織並萃取組織之RNA,並以RT-PCR技術、免疫組織染色技術與西方墨染法技術,瞭解KiSS-1與GPR54於睪丸之表現情形。 試驗結果顯示KiSS-1與GPR54在下視丘、腎臟和睪丸表現量較其他組織高,此外,GPR54另外在小腸、胰臟、卵巢和白色脂肪組織也有表現。而後也利用西方墨染法確認這項mRNA的表現結果。 而GPR54在表現位置與功能研究方面,除腦組織及癌細胞外,其它如睪丸、胰臟和小腸等組織,尚無研究證實。又因睪丸之生精作用功能與類固醇生成特性,且相關文獻並無提及kisspeptin、GPR54與睪丸之關連性,因此本試驗將以睪丸為主要研究組織,探討kisspeptin與GPR54在睪丸中之定位與功能。為了定義出kisspeptin與GPR54在睪丸中的位置,本試驗利用免疫組織染色(IHC)進行定位之實驗。結果發現kisspeptin與GPR54都高度表現於睪丸之萊吉氏細胞中,由此推測kisspptin可能分泌自萊吉氏細胞並作用於萊吉氏細胞本身而形成自我分泌(autocrine)路徑。此外,以相同試驗技術實驗於四週齡之未發身小鼠,發現未發身小鼠萊吉氏細胞之kisspeptin與GPR54表現量顯著低於發身後之小鼠。 綜上所述,HPG軸在哺乳類動物繁殖功能的維持扮演相當重要的角色,且KiSS-1基因與kisspeptin已被證明參與了繁殖系統之活化與功能。但截至目前為止只能推測其功能,而kisspeptin/GPR54系統在睪丸中更精確之生理作用尚需更多實驗證實解答,這些研究結果應能對季節性生殖的調控機制有更深入的瞭解,也將解開生殖研究領域長久存在的問題。藉由此一重大研究進展,在未來生殖生理學上將是相當重要之突破發展。 | zh_TW |
dc.description.abstract | The function of animal reproduction is mainly regulated by the hypothalamic-pituitary-gonadal (HPG) axis. As animals reach puberty, the reproductive hormones start to work. The gonadotropin releasing hormone (GnRH) from hypothalamus would provoke to increase gonadotropins, luteinizing hormone (LH) and follicle stimulating hormone (FSH) which are released from anterior pituitary. Gonadotropins stimulate gonads via the blood circulatory system to regulate the development and functions of sexual gonads. In recent years, researchers have found that GPR54, which is located in hypothalamus of human and mice can stimulate GnRH neuron to secret GnRH and subsequently activate HPG axis. KiSS-1 gene is a cancer cell metastasis suppressor. Recently, KiSS-1 has been identified as the upregulatory gene for the HPG axis. The KiSS-1 product, kisspeptin, has strong affinity to GPR54 receptor on the membrane of GnRH neuron. It can tightly bind to GPR54, and stimulate GnRH neurons to release GnRH and then activate downstream genes regulating the onset of puberty and reproductive function.
So far kisspeptin and GPR54 have been identified expressing in various tissues, but researchers were devoted to understand their role in upstream HPG axis. Therefore, their roles need to be identified in other tissues, especially in sex organ. The purpose of this study was to elucidate the expression of KiSS-1 and GPR54 in testis of mice. For this reason, thirteen-week old ICR strain mice were used in this study. The tissue samples were collected from these mice and RNA were isolated. The reverse transcription polymerase chain reaction (RT-PCR), immunohistochemistry (IHC) staining and Western blotting were used in this study. The results showed that Kiss-1 and GPR54 gene were highly expressed in hypothalamus, kidney and testis. KiSS-1 and GPR54 were also expressed in intestine, pancreas, ovary and adipose tissue. This mRNA expression data was confirmed by Western blot analysis. Due to steroidogenic and spermatogenic properties of testis, the testis was chosen for the further study. In order to identify the location of kisspeptin and GPR54 in testis, the following experiment was designed to identify the localization of kisspeptin and GPR54. From the IHC staining results, we found that both kisspeptin and GPR54 were highly expressed in interstitial cells (Leydig cells) of testis. We speculated that Leydig cells might secret kisspeptin and have autocrine characteristic. Besides, four-week old juvenile mice were taken to do the same experiments. However, less kisspeptin and GPR54 expression were found via IHC analysis. In conclusion, the HPG axis is very important in maintenance of reproduction function in mammals. The KiSS-1 and kisspeptin have been identified involved in this system. Although kisspeptin may have direct effects on the testis through autocrine route, the precise physiological role of the kisspeptin-GPR54 system in the regulation of reproductive function remains to be elucidated. | en |
dc.description.provenance | Made available in DSpace on 2021-06-15T01:19:31Z (GMT). No. of bitstreams: 1 ntu-98-R96626011-1.pdf: 4477048 bytes, checksum: 1f985bf4fffd8654fe8f9b6ee4d9f4dc (MD5) Previous issue date: 2009 | en |
dc.description.tableofcontents | 目 錄 頁次
口試委員會審定書...........................................i 謝辭......................................................ii 中文摘要.................................................iii 英文摘要...................................................v 目錄....................................................viii 圖次......................................................ix 表次.......................................................x 第一章 文獻檢討........................................1 第一節 前言...........................................1 第二節 哺乳動物發身定義與生殖生理調控機制.............3 第三節 Kisspeptin-GPR54之生理功能概論.................6 第四節 Kisspeptin-GPR54系統在生殖生理的作用機制......17 第五節 Kisspeptin-GPR54在生殖系統的研究進展..........23 第二章 動機與目的.....................................24 第三章 材料與方法.....................................25 第四章 結果...........................................32 第五章 討論...........................................36 第六章 結論...........................................40 參考文獻.................................................55 | |
dc.language.iso | zh-TW | |
dc.title | KiSS-1與GPR54在小鼠萊吉氏細胞功能之研究 | zh_TW |
dc.title | The functional study of KiSS-1 and GPR54 expression in mouse Leydig cell | en |
dc.type | Thesis | |
dc.date.schoolyear | 97-2 | |
dc.description.degree | 碩士 | |
dc.contributor.advisor-orcid | ,鍾德憲(dsjong@ntu.edu.tw) | |
dc.contributor.oralexamcommittee | 吳兩新(Leang-Shin Wu),周崇熙(Chung-Hsi Chou) | |
dc.subject.keyword | kisspeptin,GPR54,發身,HPG軸,ICR鼠,萊吉氏細胞, | zh_TW |
dc.subject.keyword | kisspeptin,GPR54,puberty,HPG axis,ICR strain mouse,Leydig cell, | en |
dc.relation.page | 62 | |
dc.rights.note | 有償授權 | |
dc.date.accepted | 2009-07-27 | |
dc.contributor.author-college | 生物資源暨農學院 | zh_TW |
dc.contributor.author-dept | 動物科學技術學研究所 | zh_TW |
顯示於系所單位: | 動物科學技術學系 |
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