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完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.advisor | 李心予(Hsinyu Lee) | |
dc.contributor.author | Yi-Long Huang | en |
dc.contributor.author | 黃宜隆 | zh_TW |
dc.date.accessioned | 2021-06-07T17:53:58Z | - |
dc.date.copyright | 2012-08-22 | |
dc.date.issued | 2012 | |
dc.date.submitted | 2012-08-17 | |
dc.identifier.citation | Selzer, A., Heart-Disease - a Textbook of Cardiovascular Medicine, 2nd Edition - Braunwald,E. New England Journal of Medicine, 1984. 310(20): p. 1337-1337.
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dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/15863 | - |
dc.description.abstract | 心血管疾病是由心臟及血管病變所引起,也是國內十大死因之一。目前治療方式主要為繞道移植手術。因此,移植材料的選擇是一個很重要的議題。其中廣泛被認知的人類臍靜脈由於是天然血管因而被認為適合用於移植。在本實驗中,我們利用SDS來清除臍靜脈上面原有的細胞群,並利用FBS進一步清除殘留的核酸以防止免疫反應的發生並藉由組織切片及DNA定量的方式來確認細胞清除的效果。繼而再將臍靜脈內皮細胞 (Human umbilical vein endothelial cells, HUVECs)及內皮前驅細胞 (Endothelial progenitor cells, EPCs)種回臍靜脈。除了讓細胞在靜止及動態的環境下貼附,我們另外在種細胞的實驗中加入鞘氨醇1-磷酸鹽 (Sphingosine1-phosphate, S1P),S1P是一種水解磷酯脂,其會調節細胞的分化、遷移及貼附。由實驗結果顯示,無論是靜態或是動態的環境下,S1P會增強內皮細胞貼附於去細胞的臍靜脈。之後的凝血時間測試顯示了有種細胞的臍靜脈有較強的抗凝血能力。我們的實驗架構中顯示此實驗提供了不同的製作血管的方法並減少人工血管的製作所需的時間。 | zh_TW |
dc.description.abstract | Cardiovascular disease (CVD), disorders of the heart and blood vessels, is the leading cause of mortality and morbidity. Arterial bypass graft is a primary therapy for the CVD patients. Therefore, choosing a proper material for arterial bypass grafting is a critical issue. Human umbilical vein (HUV) is a natural vessel and has been suggested as a suitable scaffold for vascular tissue engineering. In this study, we successfully de-cellularized HUV by using sodium dodecyl sulfate (SDS) and further incubated with medium contains 12% FBS to remove the residual nucleic acid. After the de-cellularization procedures, human umbilical vein endothelial cells (HUVECs) and endothelial progenitor cell (EPC) were then seeded back on de-cellularized HUV in the presence of 1uM sphingosine 1-phosphate (S1P) in static or rotational cultural conditions. S1P is a lysophospholipid (LPL) which binds to G protein-coupled receptors (GPCRs) and enhances endothelial cell proliferation, migration, and adhesion. Our results showed that S1P enhances endothelial attachment on de-cellularized HUV in static and rotational cultural conditions and reduces time required for preparation of vessel grafts. The finding potentially provides a novel strategy to develop vascular tissues. | en |
dc.description.provenance | Made available in DSpace on 2021-06-07T17:53:58Z (GMT). No. of bitstreams: 1 ntu-101-R99B41019-1.pdf: 1456042 bytes, checksum: 9cb1263de81426188fe6fd936c4b6a92 (MD5) Previous issue date: 2012 | en |
dc.description.tableofcontents | 口試委員會審定書……………………………………………………………………i
誌謝…………………………………………………………………………………....ii 中文摘要……………………………………………………………………………...iii ABSTRACT…………………………………………………………………………..iv INTRODUCTION…………………………………………………………………….1 Cardiovascular disease (CVD)………………………………………………………...1 Coronary artery disease (CAD)…………...…………………………………………..1 Coronary artery bypass surgery………………………………………………………..2 Human umbilical cord…………………………………………………………………3 Endothelium…………………………………………………………………………...4 Endothelium and antithrombogenicity………………………………………………...5 Endothelial progenitor cells………..…………………………………………….……6 Sphingosine-1-phosphate……………………………………………………………...6 RATIONALE………………………………………………………………………….9 MATERIALS AND METHODS……………………………………………………..10 Preparation of the human umbilical vein…………………………………………….10 Dissection of the human umbilical vein……………………………………………...10 De-cellularization of human umbilical vein…………………………………….……10 Determination of cellularity………………………………………………………….11 DNA quantification…………………………………………………………………...11 Cell culture…………………………………………………………………………...12 Cell staining…………………………………………………………………………..13 Cell treatment and seeding…………………………………………………………...14 Cell counting……………………………………………………………….…………14 Coagulation test………………………………………………………………………15 Statistical analysis……………………………………………………………………15 RESULTS…………………………………………………………………………….17 Histology analysis after de-cellularization…………………………………………..17 DNA quantification after de-cellularization…………………………………….……17 S1P enhances cell adhesion on human umbilical vein……………………………….18 Blood Compatibility…………………………………………………………………..19 DISCUSSION……………..…………………………………………………………21 Reference……………………………………………………………………………..26 FIGURES…………………………………………………………………………….34 Figures 1……………………………………………………………………………...34 Figures 2……………………………………………………………………………...36 Figures3…….………………………………………………………………….……..38 Figures 4……………………………………………………………………………...40 Figures 5……………………………………………………………………………...42 Figures 6……………………………………………………………………………...44 Figures 7……………………………………………………………………………..46 Figures 8……………………………………………………………………………...48 Figures 9…………………………………………………………………………...…50 Figures 10…………………………………………………………………………….52 | |
dc.language.iso | en | |
dc.title | 鞘氨醇1-磷酸鹽對於建構人工血管影響之探討 | zh_TW |
dc.title | Sphingosine 1-phosphate Potentiated Endothelial Cell Attachment on De-cellularized Human Umbilical Vein as a Scaffold for Vascular Tissue Engineering | en |
dc.type | Thesis | |
dc.date.schoolyear | 100-2 | |
dc.description.degree | 碩士 | |
dc.contributor.oralexamcommittee | 陳思原(Shee-Uan Chen),陸振翮(Jenher Lu) | |
dc.subject.keyword | 心血管疾病,繞道移植手術,人類臍靜脈,內皮前驅細胞,鞘氨醇1-磷酸鹽, | zh_TW |
dc.subject.keyword | cardiovascular disease,arterial bypass graft,human umbilical vein,endothelial progenitor cell,sphingosine 1-phosphate, | en |
dc.relation.page | 53 | |
dc.rights.note | 未授權 | |
dc.date.accepted | 2012-08-17 | |
dc.contributor.author-college | 生命科學院 | zh_TW |
dc.contributor.author-dept | 動物學研究所 | zh_TW |
顯示於系所單位: | 動物學研究所 |
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