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人多能干细胞中2-E2特异性表面蛋白的检测与表征

Detection and characterization of 2-E2-specific surface protein in human pluripotent stem cells.

作者信息

Kim Hana, Choi Hong Seo, Kim Cheorl-Ho, Ryu Chun Jeih

机构信息

Insitute of Bioscience, Department of Bioscience and Biotechnology, Sejong University, 98 Gunja-Dong, Gwangjin-Gu, Seoul, Korea.

出版信息

Hybridoma (Larchmt). 2011 Aug;30(4):401-4. doi: 10.1089/hyb.2011.0020.

Abstract

To investigate cell surface antigens on human embryonic stem cells (hESCs), we generated a panel of monoclonal antibodies (MAbs) against undifferentiated hESCs by a decoy immunization strategy. One of the MAbs, MAb 2-E2, specifically bound to human pluripotent stem cells but not to mouse pluripotent stem cells and mouse embryonic fibroblasts. 2-E2 also bound to human differentiated cells, peripheral blood monocytes, and dermal fibroblasts. 2-E2 antigen expression drastically decreased in retinoic acid-induced differentiated hESCs. However, it gradually increased after initial decrease during embryoid body formation of hESCs. 2-E2 recognized approximately 68 and 27 kDa proteins present on the surface of human pluripotent stem cells. The results suggest that 2-E2-specific surface protein is a novel cell surface protein that plays a role in the early differentiation of human pluripotent stem cells.

摘要

为了研究人类胚胎干细胞(hESCs)的细胞表面抗原,我们通过诱饵免疫策略制备了一组针对未分化hESCs的单克隆抗体(MAbs)。其中一种单克隆抗体,即MAb 2-E2,特异性地结合人类多能干细胞,但不结合小鼠多能干细胞和小鼠胚胎成纤维细胞。2-E2也结合人类分化细胞、外周血单核细胞和真皮成纤维细胞。在视黄酸诱导分化的hESCs中,2-E2抗原表达急剧下降。然而,在hESCs形成胚状体的过程中,它在最初下降后逐渐增加。2-E2识别出存在于人类多能干细胞表面的大约68和27 kDa的蛋白质。结果表明,2-E2特异性表面蛋白是一种新型细胞表面蛋白,在人类多能干细胞的早期分化中发挥作用。

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