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纤连蛋白-2 参与了生长中的小鼠乳腺上皮细胞外基质的早期发育。

Fibulin-2 is involved in early extracellular matrix development of the outgrowing mouse mammary epithelium.

机构信息

Institute of Cancer Sciences, College of MVLS, University of Glasgow, Glasgow, G12 8QQ, UK.

出版信息

Cell Mol Life Sci. 2014 Oct;71(19):3811-28. doi: 10.1007/s00018-014-1577-4. Epub 2014 Feb 13.

Abstract

Cell-matrix interactions control outgrowth of mammary epithelium during puberty and pregnancy. We demonstrate here that the glycoprotein fibulin-2 (FBLN2) is strongly associated with pubertal and early pregnant mouse mammary epithelial outgrowth. FBLN2 was specifically localized to the cap cells of the terminal end buds during puberty and to myoepithelial cells during very early pregnancy (days 2-3) even before morphological changes to the epithelium become microscopically visible, but was down-regulated thereafter. Exposure to exogenous oestrogen (E2) or E2 plus progesterone (P) increased Fbln2 mRNA expression in the pubertal gland, indicating hormonal control. FBLN2 was co-expressed and co-localised with the proteoglycan versican (VCAN) and co-localised with laminin (LN), while over-expression of FBLN2 in HC-11 cells increased cell adhesion to several extracellular matrix proteins including LN and fibronectin, but not collagens. Mammary glands from Fbln2 knockout mice showed no obvious phenotype but increased fibulin-1 (FBLN1) staining was detected, suggesting a compensatory mechanism by other fibulin family members. We hypothesise that similar to embryonic aortic smooth muscle development, FBLN2 and VCAN expression alters the cell-matrix interaction to allow mammary ductal outgrowth and development during puberty and to enable epithelial budding during pregnancy.

摘要

细胞-基质相互作用控制青春期和怀孕期乳腺上皮的延伸。我们在此证明,糖蛋白纤连蛋白-2(FBLN2)与青春期和早孕小鼠乳腺上皮的延伸强烈相关。FBLN2 在青春期特异性定位于终末芽的帽细胞,在早孕(第 2-3 天)甚至在肉眼可见上皮形态变化之前,定位于肌上皮细胞,但随后下调。暴露于外源性雌激素(E2)或 E2 加孕酮(P)增加了青春期腺体中 Fbln2 mRNA 的表达,表明受激素控制。FBLN2 与蛋白聚糖 versican(VCAN)共表达和共定位,与层粘连蛋白(LN)共定位,而 FBLN2 在 HC-11 细胞中的过表达增加了细胞对包括 LN 和纤维连接蛋白在内的几种细胞外基质蛋白的粘附,但不包括胶原蛋白。Fbln2 基因敲除小鼠的乳腺没有明显的表型,但检测到纤连蛋白-1(FBLN1)染色增加,表明其他纤连蛋白家族成员存在代偿机制。我们假设,类似于胚胎主动脉平滑肌的发育,FBLN2 和 VCAN 的表达改变了细胞-基质相互作用,以允许青春期乳腺导管的延伸和发育,并使怀孕期上皮芽生。

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