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胚胎干细胞向角质形成细胞的分化:野生型和β1整合素缺陷型细胞的比较。

Differentiation of embryonal stem cells into keratinocytes: comparison of wild-type and beta 1 integrin-deficient cells.

作者信息

Bagutti C, Wobus A M, Fässler R, Watt F M

机构信息

Imperial Cancer Research Fund, London, United Kingdom.

出版信息

Dev Biol. 1996 Oct 10;179(1):184-96. doi: 10.1006/dbio.1996.0250.

Abstract

beta 1 Integrins are known to regulate terminal differentiation and morphogenesis in the adult epidermis. We have investigated their role in the embryonic development of keratinocytes by comparing the differentiation of wild-type and beta 1-null mouse embryonal stem (ES) cells. By 12-15 days in culture, differentiation of embryonic or simple epithelial cells occurred in both ES cell populations, as detected by expression of keratins 8, 18, and 19. From 21 days, expression of keratins 10 and 14 and of the cornified envelope precursor involucrin indicated that some of the wild-type cells had differentiated into keratinocytes. In contrast, keratinocyte markers were not expressed in beta 1-null cultures. The beta 1-null cells failed to express the alpha 2 and alpha 3 integrin subunits on the cell surface, consistent with the association of these a subunits with beta 1. Furthermore, alpha 6 and beta 4 expression was reduced in the beta 1-null cultures. Although beta 1-null ES cells failed to undergo differentiation into keratinocytes in vitro, they did form keratinocyte cysts expressing alpha 6 beta 4, keratins 1 and 14, and involucrin when allowed to form teratomas by subcutaneous injection in mice; furthermore, beta 1-null keratinocytes were found in the epidermis of a wild-type/beta 1-null chimeric mouse. As judged by immunofluorescence microscopy, extracellular matrix assembly was severely impaired in beta 1-null ES cell cultures, but not in the teratomas or chimeric mouse skin. We therefore speculate that the failure of beta 1-null cells to differentiate into keratinocytes in vitro may reflect an inability to assemble a basement membrane.

摘要

已知β1整合素可调节成年表皮中的终末分化和形态发生。我们通过比较野生型和β1基因缺失的小鼠胚胎干细胞(ES细胞)的分化情况,研究了它们在角质形成细胞胚胎发育中的作用。在培养12 - 15天时,两个ES细胞群体中均出现了胚胎或简单上皮细胞的分化,这可通过角蛋白8、18和19的表达检测到。从21天起,角蛋白10和14以及角质化包膜前体内披蛋白的表达表明,一些野生型细胞已分化为角质形成细胞。相比之下,β1基因缺失的培养物中未表达角质形成细胞标志物。β1基因缺失的细胞未能在细胞表面表达α2和α3整合素亚基,这与这些α亚基与β1的关联一致。此外,β1基因缺失的培养物中α6和β4的表达降低。尽管β1基因缺失的ES细胞在体外未能分化为角质形成细胞,但当通过皮下注射到小鼠体内形成畸胎瘤时,它们确实形成了表达α6β4、角蛋白1和14以及内披蛋白的角质形成细胞囊肿;此外,在野生型/β1基因缺失的嵌合小鼠的表皮中发现了β1基因缺失的角质形成细胞。通过免疫荧光显微镜判断,β1基因缺失的ES细胞培养物中的细胞外基质组装严重受损,但在畸胎瘤或嵌合小鼠皮肤中则未受损。因此,我们推测β1基因缺失的细胞在体外无法分化为角质形成细胞可能反映了其无法组装基底膜。

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