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新型人类ATP结合盒转运蛋白ABCB5 P-糖蛋白对祖细胞融合的调控

Regulation of progenitor cell fusion by ABCB5 P-glycoprotein, a novel human ATP-binding cassette transporter.

作者信息

Frank Natasha Y, Pendse Shona S, Lapchak Peter H, Margaryan Armen, Shlain Debbie, Doeing Carsten, Sayegh Mohamed H, Frank Markus H

机构信息

Partners Center for Human Genetics, Harvard Medical School, Boston, MA 02115, USA.

出版信息

J Biol Chem. 2003 Nov 21;278(47):47156-65. doi: 10.1074/jbc.M308700200. Epub 2003 Sep 7.

Abstract

Cell fusion involving progenitor cells is a newly recognized phenomenon thought to contribute to tissue differentiation. The molecular mechanisms governing cell fusion are unknown. P-glycoprotein and related ATP-binding cassette transporters are expressed by progenitor cells, but their physiological role in these cell types has not been defined. Here, we have cloned ABCB5, a rhodamine efflux transporter and novel member of the human P-glycoprotein family, which marks CD133-expressing progenitor cells among human epidermal melanocytes and determines as a regulator of membrane potential the propensity of this subpopulation to undergo cell fusion. Our findings show that polyploid ABCB5+ cells are generated by cell fusion and that this process is specifically enhanced by ABCB5 P-glycoprotein blockade. Remarkably, multinucleated cell hybrids gave rise to mononucleated progeny, demonstrating that fusion contributes to culture growth and differentiation. Thus, our findings define a molecular mechanism for cell fusion involving progenitor cells and show that fusion and resultant growth and differentiation are not merely spontaneous events, but phenomena regulated by ABCB5 P-glycoprotein.

摘要

涉及祖细胞的细胞融合是一种新认识的现象,被认为有助于组织分化。控制细胞融合的分子机制尚不清楚。P-糖蛋白及相关的ATP结合盒转运蛋白由祖细胞表达,但其在这些细胞类型中的生理作用尚未明确。在此,我们克隆了ABCB5,一种若丹明流出转运蛋白,也是人类P-糖蛋白家族的新成员,它在人类表皮黑素细胞中标记表达CD133的祖细胞,并作为膜电位的调节因子决定该亚群进行细胞融合的倾向。我们的研究结果表明,多倍体ABCB5+细胞是通过细胞融合产生的,并且该过程通过ABCB5 P-糖蛋白阻断而特异性增强。值得注意的是,多核细胞杂种产生单核后代,表明融合有助于培养物的生长和分化。因此,我们的研究结果定义了一种涉及祖细胞的细胞融合分子机制,并表明融合以及由此产生的生长和分化不仅仅是自发事件,而是由ABCB5 P-糖蛋白调节的现象。

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