| Literature DB >> 34338433 |
Henrik Ortsäter1, Magda N Hernández-Vásquez1, Maria H Ulvmar1, Alexander Gow2, Taija Mäkinen1.
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 CreERT2 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-CreERT2 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-CreERT2 -mediated recombination is induced during valve leaflet formation, and efficient labeling of valve endothelial cells was observed in mature valves. The Cldn11-CreERT2 mouse thus provides a valuable tool for functional studies of valves.Entities:
Keywords: Cre recombinase; lymphatic vessel; valve
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Year: 2021 PMID: 34338433 DOI: 10.1002/dvg.23439
Source DB: PubMed Journal: Genesis ISSN: 1526-954X Impact factor: 2.487