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Distinct roles of VE-cadherin for development and maintenance of specific lymph vessel beds

Haegerling, Rene (författare)
Max Planck Inst Mol Biomed, Mammalian Cell Signaling Lab, Munster, Germany
Hoppe, Esther (författare)
Max Planck Inst Mol Biomed, Mammalian Cell Signaling Lab, Munster, Germany;Univ Munster, EIMI, Munster, Germany
Dierkes, Cathrin (författare)
Max Planck Inst Mol Biomed, Mammalian Cell Signaling Lab, Munster, Germany
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Stehling, Martin (författare)
Max Planck Inst Mol Biomed, Flow Cytometry Unit, Munster, Germany
Mäkinen, Taija (författare)
Uppsala universitet,Vaskulärbiologi
Butz, Stefan (författare)
Max Planck Inst Mol Biomed, Dept Vasc Cell Biol, Munster, Germany
Vestweber, Dietmar (författare)
Max Planck Inst Mol Biomed, Dept Vasc Cell Biol, Munster, Germany;DFG Cluster Excellence 1003 CiM Cells Mot, Munster, Germany
Kiefer, Friedemann (författare)
Max Planck Inst Mol Biomed, Mammalian Cell Signaling Lab, Munster, Germany;Univ Munster, EIMI, Munster, Germany;DFG Cluster Excellence 1003 CiM Cells Mot, Munster, Germany
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 (creator_code:org_t)
2018-10-08
2018
Engelska.
Ingår i: EMBO Journal. - : WILEY. - 0261-4189 .- 1460-2075. ; 37:22
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Endothelial cells line blood and lymphatic vessels and form intercellular junctions, which preserve vessel structure and integrity. The vascular endothelial cadherin, VE-cadherin, mediates endothelial adhesion and is indispensible for blood vessel development and permeability regulation. However, its requirement for lymphatic vessels has not been addressed. During development, VE-cadherin deletion in lymphatic endothelial cells resulted in abortive lymphangiogenesis, edema, and prenatal death. Unexpectedly, inducible postnatal or adult deletion elicited vessel bed-specific responses. Mature dermal lymph vessels resisted VE-cadherin loss and maintained button junctions, which was associated with an upregulation of junctional molecules. Very different, mesenteric lymphatic collectors deteriorated and formed a strongly hyperplastic layer of lymphatic endothelial cells on the mesothelium. This massive hyperproliferation may have been favored by high mesenteric VEGF-C expression and was associated with VEGFR-3 phosphorylation and upregulation of the transcriptional activator TAZ. Finally, intestinal lacteals fragmented into cysts or became highly distended possibly as a consequence of the mesenteric defects. Taken together, we demonstrate here the importance of VE-cadherin for lymphatic vessel development and maintenance, which is however remarkably vessel bed-specific.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Nyckelord

lymph vessels
lymphatic valves
vascular heterogeneity
VE-cadherin
YAP/TAZ

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