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作 者:王赟[1] 窦忠英[1] 乔海[1] 赵婷[1] 杨春荣[1]
机构地区:[1]西北农林科技大学国家干细胞生物技术中心陕西分中心,陕西杨凌712100
出 处:《中国农业科学》2008年第8期2554-2562,共9页Scientia Agricultura Sinica
基 金:国家"863"项目(2005AA219050);教育部重大项目(03160);国家自然科学基金(30671067);陕西省重大科技专项(2006kz05-G1)
摘 要:【目的】探寻一种简单的胰腺干细胞的分离方法,以便为糖尿病的细胞治疗研究提供丰富的种子细胞。【方法】采用胰酶消化法分离获得细胞,利用仅含有5%的血清的RPMI1640培养基培养细胞,低浓度的血清使得细胞大量死亡漂浮,只留下少数贴壁的小圆细胞。而后将血清浓度提高到15%以上继续培养;采用免疫组化方法对获得的细胞是否具有胰腺干细胞特征予以检测,并测定了细胞的生长曲线。【结果】在血清浓度提高后每个小圆细胞能快速增殖并形成一个克隆,经过这样增殖后的细胞可以连续传代,目前已传至60代。经免疫组化检测,细胞表达PDX-1、GLUT-2、vimentin等胰腺干细胞的标志;细胞也表达Glucagon、insulin、somatostatin、polypeptide等胰腺内分泌细胞的标志.【结论】通过本方法获得的细胞经检测确定为胰腺干细胞,在体外可自发分化形成胰胰内分泌部4种主要细胞。[Objective] To find an easy method for islet stem cell isolation. [Method] Cells derived from porcine fetus pancreas have been cultured in RPMI 1640 with only 5% serum. This method made most of those cells die. Only a few little cells were survived. These cells proliferated quickly when medium was changed to RPMI 1640 with 15% serum and could form cells' clone. Islet stem cell's marker was noticed and detected by immunochemical method. [Result]Cells possess strong proliferation ability and were sub cultured over 60 passages till now. It expressed islet stem cell's marker such as PDX-1, GLUT-2, and vimentin, etc. Also, it expressed insulin, Glucagon, somatostatin and polypeptide. [ Conclusion ] Cells derived by this method were determined as islet stem cells. It can differentiate into islet endocrine cell in vitro. This study has provided a reference for isolation and expansion of islet stem cell. Also, it has provided materials for diabetes therapy.
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