An inducible Cldn11-CreERT2 mouse line for selective targeting of lymphatic valves.
Henrik OrtsäterMagda N Hernández-VásquezMaria H UlvmarAlexander GowTaija MakinenPublished in: Genesis (New York, N.Y. : 2000) (2021)
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.
Keyphrases
- aortic valve
- aortic valve replacement
- transcatheter aortic valve replacement
- aortic stenosis
- transcatheter aortic valve implantation
- endothelial cells
- lymph node
- mitral valve
- high glucose
- cancer therapy
- coronary artery disease
- transcription factor
- dna damage
- dna methylation
- ejection fraction
- metabolic syndrome
- high fat diet induced
- adipose tissue
- insulin resistance
- drug delivery
- dna repair
- living cells
- skeletal muscle