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  1. NTU Theses and Dissertations Repository
  2. 工學院
  3. 應用力學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/45136
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor黃榮山(Long-Sun Huang)
dc.contributor.authorPo-Chun Tsaien
dc.contributor.author蔡伯駿zh_TW
dc.date.accessioned2021-06-15T04:05:54Z-
dc.date.available2010-02-11
dc.date.copyright2010-02-11
dc.date.issued2010
dc.date.submitted2010-02-08
dc.identifier.citation[1] P. Poredos, 'Endothelial dysfunction in the pathogenesis of atherosclerosis,' Clin Appl Thromb Hemost, vol. 7, pp. 276-280, Oct 2001.
[2] P. V. Targonski, P. O. Bonetti, G. M. Pumper, S. T. Higano, D. R. Holmes, Jr., and A. Lerman, 'Coronary endothelial dysfunction is associated with an increased risk of cerebrovascular events,' Circulation, vol. 107, pp. 2805-2809, Jun 10 2003.
[3] K. Kathir and M. R. Adams, 'Endothelial dysfunction as a predictor of acute coronary syndromes,' Semin Vasc Med, vol. 3, pp. 355-362, Nov 2003.
[4] D. L. Fry, 'Acute vascular endothelial changes associated with increased blood velocity gradients,' Circ Res, vol. 22, pp. 165-197, Feb 1968.
[5] G. M. Walker, H. C. Zeringue, and D. J. Beebe, 'Microenvironment design considerations for cellular scale studies,' Lab Chip, vol. 4, pp. 91-97, Apr 2004.
[6] M. S. Tsai, S. M. Hwang, Y. L. Tsai, F. C. Cheng, J. L. Lee, and Y. J. Chang, 'Clonal amniotic fluid-derived stem cells express characteristics of both mesenchymal and neural stem cells,' Biol Reprod, vol. 74, pp. 545-551, Mar 2006.
[7] P. De Coppi, G. Bartsch, Jr., M. M. Siddiqui, T. Xu, C. C. Santos, L. Perin, G. Mostoslavsky, A. C. Serre, E. Y. Snyder, J. J. Yoo, M. E. Furth, S. Soker, and A. Atala, 'Isolation of amniotic stem cell lines with potential for therapy,' Nat Biotechnol, vol. 25, pp. 100-106, Jan 2007.
[8] M. H. Ross, Histology: A Text and Atlas, Third Edition ed.: Lippincott Williams & Wilkins, 1995.
[9] C. F. Dewey, Jr., 'Effects of fluid flow on living vascular cells,' J Biomech Eng, vol. 106, pp. 31-35, Feb 1984.
[10] J. A. Frangos, S. G. Eskin, L. V. McIntire, and C. L. Ives, 'Flow effects on prostacyclin production by cultured human endothelial cells,' Science, vol. 227, pp. 1477-1479, Mar 22 1985.
[11] S. Akimoto, M. Mitsumata, T. Sasaguri, and Y. Yoshida, 'Laminar shear stress inhibits vascular endothelial cell proliferation by inducing cyclin-dependent kinase inhibitor p21(Sdi1/Cip1/Waf1),' Circ Res, vol. 86, pp. 185-190, Feb 4 2000.
[12] H. Wang, G. M. Riha, S. Yan, M. Li, H. Chai, H. Yang, Q. Yao, and C. Chen, 'Shear stress induces endothelial differentiation from a murine embryonic mesenchymal progenitor cell line,' Arterioscler Thromb Vasc Biol, vol. 25, pp. 1817-1823, Sep 2005.
[13] K. Yamamoto, T. Takahashi, T. Asahara, N. Ohura, T. Sokabe, A. Kamiya, and J. Ando, 'Proliferation, differentiation, and tube formation by endothelial progenitor cells in response to shear stress,' J Appl Physiol, vol. 95, pp. 2081-2088, Nov 2003.
[14] C. C. Wu, Y. C. Chao, C. N. Chen, C. Shu, Y. C. Chen, C. C. Chien, J. J. Chiu, and B. L. Yen, 'Synergism of biochemical and mechanical stimuli in the differentiation of human placenta-derived multipotent cells into endothelial cells,' Journal of biomechanics, vol. 41, pp. 813-821, Nov 2008.
[15] 福井三郎, 杉野幸夫, 細胞培養: 藝軒圖書, 1989.
[16] H. Takamatsu and N. Kumagae, 'Survival of biological cells deformed in a narrow gap,' J Biomech Eng, vol. 124, pp. 780-783, Dec 2002.
[17] E. Bramanti, F. Ferri, C. Sortino, M. Onor, G. Raspi, and M. Venturini, 'Characterization of denatured proteins by hydrophobic interaction chromatography: a preliminary study,' Biopolymers, vol. 69, pp. 293-300, Jul 2003.
[18] P. J. Torry, G. T. Taylor, M. Nullet, S. K. Sharma and B. E. Liebert, 'Protein adsorption from seawater onto solid substrata: II. Behavior of bound protein and its influence on interfacial proteins,' Mar. Chem, vol. 47(1), pp. 21-39, 1994.
[19] N. Q. Balaban, U. S. Schwarz, D. Riveline, P. Goichberg, G. Tzur, I. Sabanay, D. Mahalu, S. Safran, A. Bershadsky, L. Addadi, and B. Geiger, 'Force and focal adhesion assembly: a close relationship studied using elastic micropatterned substrates,' Nat Cell Biol, vol. 3, pp. 466-472, May 2001.
[20] A. I. Teixeira, G. A. Abrams, P. J. Bertics, C. J. Murphy, and P. F. Nealey, 'Epithelial contact guidance on well-defined micro- and nanostructured substrates,' J Cell Sci, vol. 116, pp. 1881-192, May 2003.
[21] C. S. Chen, J. L. Alonso, E. Ostuni, G. M. Whitesides, and D. E. Ingber, 'Cell shape provides global control of focal adhesion assembly,' Biochem Biophys Res Commun, vol. 307, pp. 355-361, Jul 2003.
[22] C. M. Nelson and C. S. Chen, 'Cell-cell signaling by direct contact increases cell proliferation via a PI3K-dependent signal,' FEBS Lett, vol. 514, pp. 238-242, Mar 2002.
[23] X. F. Walboomers, H. J. Croes, L. A. Ginsel, and J. A. Jansen, 'Growth behavior of fibroblasts on microgrooved polystyrene,' Biomaterials, vol. 19, pp. 1861-1868, Oct 1998.
[24] S. Chang, Y. Popowich, R. S. Greco, and B. Haimovich, 'Neutrophil survival on biomaterials is determined by surface topography,' J Vasc Surg, vol. 37, pp. 1082-1090, May 2003.
[25] M. Hirashima, H. Kataoka, S. Nishikawa, and N. Matsuyoshi, 'Maturation of embryonic stem cells into endothelial cells in an in vitro model of vasculogenesis,' Blood, vol. 93, pp. 1253-1263, Feb 15 1999.
[26] H. Wang, G. M. Riha, S. Yan, M. Li, H. Chai, H. Yang, Q. Yao, and C. Chen, 'Shear Stress Induces Endothelial Differentiation From a Murine Embryonic Mesenchymal Progenitor Cell Line,' Arterioscler Thromb Vasc Biol, vol. 25, pp. 1817-1823, Sep 2005.
[27] J. Ando, H. Nomura, and A. Kamiya, 'The effect of fluid shear stress on the migration and proliferation of cultured endothelial cells,' Microvasc Res, vol. 33, pp. 62-70, Jan 1987.
[28] W. B. Amos and J. G. White, 'How the confocal laser scanning microscope entered biological research,' Biol Cell, vol. 95, pp. 335-342, Sep 2003.
[29] J. C. Voyta, D. P. Via, C. E. Butterfield, and B. R. Zetter, 'Identification and isolation of endothelial cells based on their increased uptake of acetylated-low density lipoprotein,' J Cell Biol, vol. 99, pp. 2034-2040, Dec 1984.
[30] S. Chien, 'Mechanotransduction and endothelial cell homeostasis: the wisdom of the cell,' Am J Physiol Heart Circ Physiol, vol. 292, pp. H1209-H1224, Mar 2007.
[31] 蔣雅郁, '微流體剪應力對內皮細胞與多能羊水幹細胞分化之影響,' Jul 2008.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/45136-
dc.description.abstract幹細胞治療在心血管疾病的應用上漸漸受到關注,利用微機電製程製造的微晶片,提供比公分尺寸的實驗更接近人體的培養環境,例如細胞和細胞間的距離以及類似人體血管的培養體積,在這理論基礎下,微機電技術製造的微晶片提供流體剪應力的刺激,可以加速羊水幹細胞分化成內皮細胞
內皮細胞有沿著流場方向排列的特性,匯整人類羊水幹細胞在12 dyne/cm2
剪應力刺激24小時後的排列方向統計資料,剪應力刺激3小時後的排列角度分布和24小時的結果接近,表示其有相近的分化結果,此外,剪應力12 dyne/cm2 作用3小時以及24小時後,血小板與內皮細胞貼附分子(platelet endothelial cell adhesion molecule ,PECAM-1) 和 溫偉伯因子(von Willebrand Factor, vWF)都有明顯的表現,經過3小時的剪應力刺激,血小板與內皮細胞貼附分子, 溫偉伯因子以及血管內皮生長因子受體(vascular endothelial growth factor-2 receptor, VEGFR)的基因表現量都超過10倍以上,另外經過剪應力刺激後,在基質膠(matrigel) 基底上,觀察到低密度脂蛋白的堆積以及網狀結構形成,細胞在剪應力12 dyne/cm2 刺激下,分化程度比3, 6, and 18 dyne/cm2來的高
在巨觀尺寸的實驗架構下,需要數天才能達到分化的結果,而微流道系統成功的提供了快速分化的環境,人類羊水細胞在微流道系統的培養環境下,3小時就有明顯分化結果,本研究顯現出其在幹細胞的治療以及心血管疾病的研究上的潛力
zh_TW
dc.description.abstractStem cell therapies for cardiovascular diseases are of great growing interest. Micro-electro-mechanism-system (MEMS) fabricated chips provide more in vivo like cell-to-cell distance and culturing volume than that in centimetre-scaled experiments. In this thesis, we are able to accelerate the process of endothelial differentiation of human amniotic fluid stem cells (hAFSCs) by the stimulation of fluidic shear stress in a MEMS-fabricated micro device.
Cells aligning to flow directions is a known property of endothelial cells. hAFSCs affected by 12 dyne/cm2 of shear stress were compiled statistics for the arrangement angles toward the flow direction in a 24-hour period. The angular distribution of cells after 3 hours of stress stimulation approaches to that of cells after 24 hours, indicating similar degrees of endothelial differentiation. Both cell samples stimulated by 12 dyne/cm2 stress after 3 hours and 24 hours exhibit protein expressions of platelet endothelial cell adhesion molecule (PECAM-1) and von Willebrand Factor (vWF). Over ten folds of gene expressions in PECAM-1, vWF and vascular endothelial growth factor-2 receptor (VEGFR) appeared after 3 hours stimulation. Uptakes of ac-LDL and formation of tube-like structure on Matrigel were also observed after shear stress stimulation. Cells stimulated by 12dyne/cm2 shear stress have higher degrees of differentiation than those stimulated by 3, 6, and 18 dyne/cm2 shear stress.
Utilizing 3 hours to achieve differentiation instead of days in macro-scale experiments, this micro fluidic system has been proved successful for a rapid shear stress stimulation of hAFSCs differentiation into endothelial cells. This research shows its great potential in stem cell therapy and cardiovascular disease studies.
en
dc.description.provenanceMade available in DSpace on 2021-06-15T04:05:54Z (GMT). No. of bitstreams: 1
ntu-99-R96543051-1.pdf: 5275540 bytes, checksum: ea53400f11008b2688edff1162c15f97 (MD5)
Previous issue date: 2010
en
dc.description.tableofcontents第一章 序論 1
1-1 前言 1
1-2 研究動機 3
1-3 文獻探討 5
1-4 研究方法 10
1-5 論文架構 11
第二章 實驗原理 12
2-1 細胞培養環境之控制 12
2-1-1 傳統細胞培養技術 12
2-1-2 微尺寸培養對細胞之影響 16
2-2 流體剪應力對細胞之影響與計算 19
2-3 流體剪應力對幹細胞分化為內皮細胞之影響 22
2-4 即時定量聚合酶連鎖反應 24
2-5 雷射共軛焦顯微鏡 25
2-6 血管生成與低密度脂蛋白攝取 26
第三章 製程設計與實驗方法 26
3-1 微流道晶片設計與製造 27
3-1-1 微流道晶片規格與設計 27
3-1-2 聚二甲基矽氧烷微流道製作 28
3-1-3 微流道晶片整合 29
3-2 實驗系統之架設 31
3-3 羊水幹細胞之培養 32
3-4 羊水幹細胞之剪應力刺激 33
第四章 實驗結果 35
4-1 羊水幹細胞受剪應力影響之排列效果 35
4-2 羊水幹胞受剪應力影響後之基因型表現 41
4-3 羊水幹胞受剪應力影響後之蛋白質表現 42
4-4 羊水幹細胞受剪應力影響後之血管生成實驗 46
第五章 結論以及未來展望 48
5-1 結論 48
5-2 未來展望 49
參考文獻 51
dc.language.isozh-TW
dc.subject幹細胞zh_TW
dc.subject微流體zh_TW
dc.subject內皮細胞zh_TW
dc.subjectmicro fluidicsen
dc.subjectstem cellen
dc.subjectendothelial cellsen
dc.title微流體剪應力對羊水幹細胞分化為內皮細胞之影響zh_TW
dc.titlethe effects of microfluidic shear stress on endothelial differentiation of amniotic fluid stem cellsen
dc.typeThesis
dc.date.schoolyear98-1
dc.description.degree碩士
dc.contributor.oralexamcommittee黃效民(Shiaw-Min Hwang),王安邦(An-Bang Wang)
dc.subject.keyword幹細胞,微流體,內皮細胞,zh_TW
dc.subject.keywordstem cell,micro fluidics,endothelial cells,en
dc.relation.page53
dc.rights.note有償授權
dc.date.accepted2010-02-09
dc.contributor.author-college工學院zh_TW
dc.contributor.author-dept應用力學研究所zh_TW
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