重組及培養人類誘導型多能性幹細胞在奈米片段接枝表面;Reprogramming and Culture of Human Induced Pluripotent Stem Cells on a Substrate with Immobilized Cell Adhesion Peptides

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題名:	重組及培養人類誘導型多能性幹細胞在奈米片段接枝表面;Reprogramming and Culture of Human Induced Pluripotent Stem Cells on a Substrate with Immobilized Cell Adhesion Peptides
作者:	林佳逸;Lin,Jia-yi
貢獻者:	化學工程與材料工程學系
關鍵詞:	多能性幹細胞;生醫材料;pluripotent stem cell;Cell Adhesion Peptides
日期:	2014-06-16
上傳時間:	2014-08-11 18:13:51 (UTC+8)
出版者:	國立中央大學
摘要:	人類誘導型多能性幹細胞由於具有分化成三胚層細胞之能力，在臨床上相當具有潛力用於許多疾病的治療。然而人類誘導型多能性幹細胞由於飼養層具有異種來源，在臨床上發展受到許多限制。使用具有奈米片段表面改質之生醫材料在無飼養層之培養環境下，可以提供具有再現性的培養環境、低成本的培養材料並且不會引入異種汙染源。這些條件將可以改善人類誘導型多能性幹細胞在臨床上之運用。在這篇文章中我們在使用老鼠胚胎纖維母細胞作為飼養層環境下，成功利用具有多能性基因之逆轉錄病毒，將人類脂肪幹細胞誘導成人類誘導型多能性幹細胞。人類誘導型多能性幹細胞群落可以在病毒轉染後第八天觀察到，從一開始種植105個人類脂肪幹細胞，經過誘導後可以在10cm飼養層上總共得到484個群落，而其誘導成多能性幹細胞之效率為0.484%。此外，鹼性磷酸酶活性及多能性蛋白指標Oc4,Sox2及SSEA-4都清楚的表現在人類誘導型多能性幹細胞之群落上。我們同時也利用聚乙烯醇-共-衣康酸之薄膜上接枝奈米片段，建立新的無飼養層之培養系統用於培養人類多能性幹細胞。在這篇研究中，隨著增加由玻連蛋白中找到之寡胜肽的濃度，人類多能性幹細胞將表現較高之群落貼附率、較高群落數放大率及較低群落分化率。此外也利用控制聚乙烯醇-共-衣康酸薄膜之交聯時間，調控薄膜之表面軟硬度，從10.3千帕斯卡至30.4千帕斯卡。在這裡使用人類胚胎幹細胞(WA09)培養在具有較硬表面之聚乙烯醇-共-衣康酸細胞培養系統，比起較表面具有較好的表現。另外，在經過數代培養在表面接枝500毫克/毫升濃度之寡胜肽在25.3千帕斯卡表面軟硬度之聚乙烯醇-共-衣康酸細胞培養系統，人類胚胎幹細胞群落仍然表現鹼性磷酸酶活性及多能性蛋白指標Oct4、Sox2、Nanog、SSEA-4、Tra-1-60及Tra-1-81。這些結果顯示人類多能性幹細胞可以培養在我們的聚乙烯醇-共-衣康酸細胞培養系統，並且維持人類幹細胞之多能性表現。在未來，聚乙烯醇-共-衣康酸細胞培養系統可用作具有無異種來源及無飼養層之培養環境來誘導人類組織細胞形成人類多能性幹細胞。 ;Human induced pluripotent stem cells (hiPSCs) have significant potential in therapeutic applications for many diseases because they have the specific ability to differentiate into all types of human somatic cells. However, the tentative clinical potential of hiPSCs is restricted by the use of mouse embryonic fibroblasts (MEFs) as a feeder layer. The feeder-free cultures using synthetic biomaterials having nanosegments as stem cell culture materials offer more reproducible culture conditions and lower the cost of production without introducing xenogenic contaminants. These improvements will increase the potential clinical applications of differentiated hiPSCs. Here we report that hiPSCs can be successively generated with usage of a feeder layer of MEFs during generation of hiPSCs by transfection of retrovirus containing pluripotent genes into human adipose-derived stem cells (hADSCs). hiPSC colonies were clearly observed for the cells cultured on MEFs at day 8 after transfection The number of colonies generated on MEFs was 484 per 10 cm dishes, when 105 hADSCs were seeded on the dishes. The efficiency of hiPSC generation on MEFs was 0.484%. Furthermore, the hiPSC colony showed alkali phosphatase activity clearly, and immunofluorescence suggested that the hiPSCs were generated on MEFs expressing pluripotent protein of Oct4, Sox2 and SSEA-4. At same time, polyvinylalcohol-co-itaconic acid (PVA-IA) films grafted with nanosegment (KGGPQVTRGDVFTMP [cell-binding domain derived from vitronectin, oligoVN] was established for cultivation of human pluripotent stem cells. In this study, with increase the concentration of oligo-VN, hPSCs shown the higher colony attachment ratio, colony expansion fold and lower differentiation ratio. Furthermore, the elasticity of PVA-IA films grafted with oligo-VN was regulated from 10.3 kPa to 30.4kPa by control of crosslinking time of PVA-IA. hESCs (WA09) cultured on PVA-IA culture system with stiffer elasticity of surface (25.3kPa) shown the better performance than the soft one (15.8kPa). Moreover, hESCs (WA09) cultured on PVA-IA films grafted with 500µg/ml oligo-VN with 25.3kPa elasticity of surface for 5 passage shown alkali phosphatase activity and pluripotent protein expression such as Oct4, Sox2, Nanog, SSEA-4, Tra-1-60 and Tra-1-81. This result indicates that hPSCs could be cultured on our PVA-IA culture system and maintain pluripotency of hPSCs. In the future, the PVA-IA culture system could be used to generation of hiPSCs from primary human tissue cells on xenogenic-free and feeder-free conditions.
顯示於類別:	[化學工程與材料工程研究所] 博碩士論文

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