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诱导型 Claudin11-CreER 小鼠品系用于选择性靶向淋巴管瓣膜。

An inducible Cldn11-CreER mouse line for selective targeting of lymphatic valves.

机构信息

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.

Department of Neurology and Pediatrics, Center for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan, USA.

出版信息

Genesis. 2021 Aug;59(7-8):e23439. doi: 10.1002/dvg.23439. Epub 2021 Aug 2.

Abstract

Luminal valves of collecting lymphatic vessels are critical for maintaining unidirectional flow of lymph and their dysfunction underlies several forms of primary lymphedema. Here, we report on the generation of a transgenic mouse expressing the tamoxifen inducible CreER under the control of Cldn11 promoter that allows, for the first time, selective and temporally controlled targeting of lymphatic valve endothelial cells. We show that within the vasculature CLDN11 is specifically expressed in lymphatic valves but is not required for their development as mice with a global loss of Cldn11 display normal valves in the mesentery. Tamoxifen treated Cldn11-CreER mice also carrying a fluorescent Cre-reporter displayed reporter protein expression selectively in lymphatic valves and, to a lower degree, in venous valves. Analysis of developing vasculature further showed that Cldn11-CreER -mediated recombination is induced during valve leaflet formation, and efficient labeling of valve endothelial cells was observed in mature valves. The Cldn11-CreER mouse thus provides a valuable tool for functional studies of valves.

摘要

淋巴管腔瓣膜对于维持淋巴单向流动至关重要,其功能障碍是几种原发性淋巴水肿的基础。在这里,我们报告了一种在 Cldn11 启动子控制下表达他莫昔芬诱导型 CreER 的转基因小鼠的产生,这使得首次能够选择性和时间控制地靶向淋巴管瓣膜内皮细胞。我们发现,在脉管系统中,CLDN11 特异性表达于淋巴管瓣膜中,但对于其发育并非必需,因为全身缺失 Cldn11 的小鼠在肠系膜中显示出正常的瓣膜。用他莫昔芬处理的 Cldn11-CreER 小鼠,其携带荧光 Cre 报告基因,也选择性地在淋巴管瓣膜中表达报告蛋白,在静脉瓣膜中表达程度较低。对发育中的脉管系统的分析进一步表明,Cldn11-CreER 介导的重组发生在瓣膜小叶形成过程中,在成熟瓣膜中观察到有效的瓣膜内皮细胞标记。因此,Cldn11-CreER 小鼠为瓣膜的功能研究提供了一个有价值的工具。

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