請用此 Handle URI 來引用此文件:
http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/50768
完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.advisor | 郭柏齡(Po-Ling Kuo) | |
dc.contributor.author | PHUNG HAO DINH | en |
dc.contributor.author | 馮浩穎 | zh_TW |
dc.date.accessioned | 2021-06-15T12:57:15Z | - |
dc.date.available | 2021-07-26 | |
dc.date.copyright | 2016-07-26 | |
dc.date.issued | 2016 | |
dc.date.submitted | 2016-07-14 | |
dc.identifier.citation | 1. George, J., et al., Dimethylnitrosamine-induced liver injury in rats: the early deposition of collagen. Toxicology, 2001. 156(2–3): p. 129-138.
2. Budny, T., et al., Morphologic features in the regenerating liver—a comparative intravital, lightmicroscopical and ultrastructural analysis with focus on hepatic stellate cells. Virchows Archiv, 2007. 451(4): p. 781-791. 3. Friedman, S.L., et al., Hepatic lipocytes: the principal collagen-producing cells of normal rat liver. Proceedings of the National Academy of Sciences of the United States of America, 1985. 82(24): p. 8681-8685. 4. Atzori, L., G. Poli, and A. Perra, Hepatic stellate cell: A star cell in the liver. The International Journal of Biochemistry & Cell Biology, 2009. 41(8–9): p. 1639-1642. 5. McCuskey, R.S., The Hepatic Microvascular System in Health and Its Response to Toxicants. The Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology, 2008. 291(6): p. 661-671. 6. Ballardini, G., et al., Desmin and actin in the identification of Ito cells and in monitoring their evolution to myofibroblasts in experimental liver fibrosis. Virchows Archiv B, 1988. 56(1): p. 45-49. 7. Kawada, N., et al., The contraction of hepatic stellate (Ito) cells stimulated with vasoactive substances. European Journal of Biochemistry, 1993. 213(2): p. 815-823. 8. Glicklis, R., et al., Hepatocyte behavior within three-dimensional porous alginate scaffolds. Biotechnology and Bioengineering, 2000. 67(3): p. 344-353. 9. Kikuchi, A. and T. Okano, Nanostructured designs of biomedical materials: applications of cell sheet engineering to functional regenerative tissues and organs. Journal of Controlled Release, 2005. 101(1–3): p. 69-84. 10. Ho, C.-T., et al., Liver-cell patterning Lab Chip: mimicking the morphology of liver lobule tissue. Lab on a Chip, 2013. 13(18): p. 3578-3587. 11. Halldorsson, S., et al., Advantages and challenges of microfluidic cell culture in polydimethylsiloxane devices. Biosensors and Bioelectronics, 2015. 63: p. 218-231. 12. Kilian, K.A., et al., Geometric cues for directing the differentiation of mesenchymal stem cells. Proceedings of the National Academy of Sciences of the United States of America, 2010. 107(11): p. 4872-4877. 13. O'Brien, L.E., M.M.P. Zegers, and K.E. Mostov, Building epithelial architecture: insights from three-dimensional culture models. Nat Rev Mol Cell Biol, 2002. 3(7): p. 531-537. 14. Shamir, E.R. and A.J. Ewald, Three-dimensional organotypic culture: experimental models of mammalian biology and disease. Nature reviews. Molecular cell biology, 2014. 15(10): p. 647-664. 15. Tanaka, H., et al., Chondrogenic differentiation of murine embryonic stem cells: Effects of culture conditions and dexamethasone. Journal of Cellular Biochemistry, 2004. 93(3): p. 454-462. 16. Toh, Y.-C., et al., A microfluidic 3D hepatocyte chip for drug toxicity testing. Lab on a Chip, 2009. 9(14): p. 2026-2035. 17. Shin, Y., et al., Microfluidic assay for simultaneous culture of multiple cell types on surfaces or within hydrogels. Nat. Protocols, 2012. 7(7): p. 1247-1259. 18. Masaya Oda, H.Y., Jing-Yan Han, Regulatory mechanisms of hepatic microcirculation. Clinical Hemorheology and Microcirculation, 2003. 29(3-4): p. 167-182. 19. Cho, H., et al., How the capillary burst microvalve works. Journal of Colloid and Interface Science, 2007. 306(2): p. 379-385. 20. Moreno-Arotzena, O., et al., Characterization of Fibrin and Collagen Gels for Engineering Wound Healing Models. Materials, 2015. 8(4): p. 1636. 21. Serpooshan, V., et al., Hydraulic permeability of multilayered collagen gel scaffolds under plastic compression-induced unidirectional fluid flow. Acta Biomaterialia, 2013. 9(1): p. 4673-4680. 22. Knapp, D.M., et al., Rheology of reconstituted type I collagen gel in confined compression. Journal of Rheology, 1997. 41(5): p. 971-993. 23. Birukawa, N.K., et al., Activated hepatic stellate cells are dependent on self collagen, cleaved by membrane type 1-matrix metalloproteinase for their growth. Journal of Biological Chemistry, 2014. 24. Okada, Y., et al., Pressure loading and ethanol exposure differentially modulate rat hepatic stellate cell activation. Journal of Cellular Physiology, 2008. 215(2): p. 472-480. 25. Guvendiren, M., et al., Hydrogels with differential and patterned mechanics to study stiffness-mediated myofibroblastic differentiation of hepatic stellate cells. Journal of the Mechanical Behavior of Biomedical Materials, 2014. 38: p. 198-208. 26. Laleman, W., et al., Portal hypertension: from pathophysiology to clinical practice. Liver International, 2005. 25(6): p. 1079-1090. 27. Senoo, H.I., Katsuyuki; Sato, Mitsuru; Kojima, Naosuke; Miura, Mitsutaka; Hata, Ruy-Ichiro, Three-dimensional structure of extracellular matrix reversibly regulates morphology, proliferation, and collagen metabolism of perisinusoidal stellate cells (Vitamin A-storing cells). Cell Biology International. 20(7): p. 501-512. 28. Yi, S.-H., et al., Mechanical force and tensile strain activated hepatic stellate cells and inhibited retinol metabolism. Biotechnology Letters, 2015. 37(6): p. 1141-1152. | |
dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/50768 | - |
dc.description.abstract | 肝臟星狀細胞在肝硬化的形成扮演了非常重要的腳色:製造大量的組織纖維,提高肝臟竇狀間隙的壓力以及門脈高壓等。然而,過去的研究大多注重於化學因子的研究,而物理性刺激如間隙內的高壓,血流造成的剪應力等常被忽略。在此研究中,我們發展了一個能夠模擬肝臟竇狀間隙周圍物理環境的三維細胞培養之微流道平台,來研究水壓對於肝臟星狀細胞的影響。 | zh_TW |
dc.description.abstract | Hepatic stellate cells (HSCs) play a crucial role in the development of liver fibrosis which is characterized by massive tissue scarring, elevated hepatic sinusoidal pressure, and portal hypertension. However, while a multitude of chemical factors have been investigated in the pathogenesis of liver fibrosis, physical factors such as elevated hydrostatic pressure and shear stress caused by blood flow in sinusoids remain unclear. In this study, we developed a 3D cell culture microfluidic platform that mimics the physical environments of hepatic sinusoids to investigate the effects of elevated hydrostatic pressure on HSCs phenotypes. | en |
dc.description.provenance | Made available in DSpace on 2021-06-15T12:57:15Z (GMT). No. of bitstreams: 1 ntu-105-R02945043-1.pdf: 3072665 bytes, checksum: 545fde5e31e447e7922f47faf801d45d (MD5) Previous issue date: 2016 | en |
dc.description.tableofcontents | 致謝 1
摘要 3 Abstract 4 Content 5 Chapter 1. Introduction 7 Chapter 2. Materials and Methods 12 2.1 Device design and operation principle 12 2.2 Fabrication of microfluidic system 23 2.3 Hydrostatic pressure application and measurement 26 2.4 COMSOL simulation 27 2.4 Cell culture and collagen gel preparation 27 2.5 Image acquisition 28 2.6 Cell staining, imaging and quantification 30 Chapter 3. Results and Discussions 32 3.1 Simulated pressure field and flow rates 32 3.1.1 Water-filled-only: 32 3.1.2 Half-gel and Double-gel: 35 3.1.3 Full-gel: 38 3.1.4 Comparison between no-gel, half-gel and full-gel: 39 3.2 Comparison of pressure between experiment and simulation 41 3.3 HSCs in the device 45 Chapter 4. Conclusions 48 References 50 | |
dc.language.iso | en | |
dc.title | 可模擬肝臟竇狀間隙高壓之三維細胞培養平台 | zh_TW |
dc.title | A 3D cell culture platform for mimicking pressurized hepatic sinusoid | en |
dc.type | Thesis | |
dc.date.schoolyear | 104-2 | |
dc.description.degree | 碩士 | |
dc.contributor.oralexamcommittee | 林致廷(Chih-Ting Lin),趙本秀(Pen-Hsiu Chao),蘇裕家(Yu-Chia Su) | |
dc.subject.keyword | 肝臟星狀細胞,肝臟竇狀間隙,壓力,三維細胞培養,微流道, | zh_TW |
dc.subject.keyword | Hepatic stellate cells (HSCs),hepatic sinusoids,pressure,3D cell culture,microfluidics, | en |
dc.relation.page | 52 | |
dc.identifier.doi | 10.6342/NTU201600869 | |
dc.rights.note | 有償授權 | |
dc.date.accepted | 2016-07-14 | |
dc.contributor.author-college | 電機資訊學院 | zh_TW |
dc.contributor.author-dept | 生醫電子與資訊學研究所 | zh_TW |
顯示於系所單位: | 生醫電子與資訊學研究所 |
文件中的檔案:
檔案 | 大小 | 格式 | |
---|---|---|---|
ntu-105-1.pdf 目前未授權公開取用 | 3 MB | Adobe PDF |
系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。