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内黏液素在小鼠胚胎内皮以及背主动脉中假定造血簇上的早期表达。

Early expression of endomucin on endothelium of the mouse embryo and on putative hematopoietic clusters in the dorsal aorta.

作者信息

Brachtendorf G, Kuhn A, Samulowitz U, Knorr R, Gustafsson E, Potocnik A J, Fässler R, Vestweber D

机构信息

Institute of Cell Biology, ZMBE, University of Münster and Max-Planck-Institute of Physiological and Clinical Research, Bad Nauheim, Germany.

出版信息

Dev Dyn. 2001 Nov;222(3):410-9. doi: 10.1002/dvdy.1199.

Abstract

Endomucin is a recently identified sialomucin that is specifically expressed on endothelium of the adult mouse. Here, we have analysed the expression of endomucin during development of the vascular system by immunohistochemistry by using three monoclonal antibodies (mAb). We demonstrate that two of the mAb, V.5C7 and V.1A7, recognize epitopes on the nonglycosylated protein, because they recognize the antigen when it is synthesized as a bacterial fusion protein and when it is in vitro translated in a membrane-free reticulocyte lysate. During in vitro differentiation of embryonic stem cells to endothelial cells, endomucin is expressed at day 6 after onset of differentiation, 1 day later than PECAM-1. During differentiation of the mouse embryo, endomucin is first detected at E8.0 in all embryonic blood vessels detectable at this stage but is absent in blood islands of the yolk sac. Analysing the paraaortic-splanchnopleura (P-SP) region and the aorta-gonad-mesonephros (AGM) region as sites of intraembryonic hematopoiesis, we found that endothelium of the dorsal aorta is brightly positive for endomucin at E8.5-9.0 and at E11.5. At later stages and in the adult aorta, endothelial staining is strongly reduced and confined to focal areas. Cell clusters associated with the luminal surface of the endothelium of the dorsal aorta could be stained for endomucin and for CD34. At a later stage (E15.5) single leukocytes in the lumen of large venules were stained for endomucin. We conclude that endomucin is an early endothelial-specific antigen that is also expressed on putative hematopoietic progenitor cells.

摘要

内联蛋白是一种最近发现的涎黏蛋白,在成年小鼠的内皮细胞上特异性表达。在此,我们使用三种单克隆抗体(mAb),通过免疫组织化学分析了血管系统发育过程中内联蛋白的表达。我们证明其中两种mAb,V.5C7和V.1A7,识别非糖基化蛋白上的表位,因为当抗原作为细菌融合蛋白合成时以及在无膜网织红细胞裂解物中进行体外翻译时,它们都能识别该抗原。在胚胎干细胞体外分化为内皮细胞的过程中,内联蛋白在分化开始后第6天表达,比血小板内皮细胞黏附分子-1(PECAM-1)晚1天。在小鼠胚胎分化过程中,内联蛋白在E8.0时首次在该阶段可检测到的所有胚胎血管中被检测到,但在卵黄囊的血岛中不存在。分析主动脉旁脏壁中胚层(P-SP)区域和主动脉-性腺-中肾(AGM)区域作为胚胎内造血的部位,我们发现背主动脉的内皮在E8.5-9.0和E11.5时对内联蛋白呈强阳性。在后期和成年主动脉中,内皮染色强烈减少并局限于局部区域。与背主动脉内皮腔表面相关的细胞簇对内联蛋白和CD34均可染色。在后期阶段(E15.5),大静脉管腔中的单个白细胞对内联蛋白呈阳性染色。我们得出结论,内联蛋白是一种早期内皮特异性抗原,也在假定的造血祖细胞上表达。

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