Publikationsdatum:
1999-05-29
Beschreibung:
Endoglin is a transforming growth factor-beta (TGF-beta) binding protein expressed on the surface of endothelial cells. Loss-of-function mutations in the human endoglin gene ENG cause hereditary hemorrhagic telangiectasia (HHT1), a disease characterized by vascular malformations. Here it is shown that by gestational day 11.5, mice lacking endoglin die from defective vascular development. However, in contrast to mice lacking TGF-beta, vasculogenesis was unaffected. Loss of endoglin caused poor vascular smooth muscle development and arrested endothelial remodeling. These results demonstrate that endoglin is essential for angiogenesis and suggest a pathogenic mechanism for HHT1.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Li, D Y -- Sorensen, L K -- Brooke, B S -- Urness, L D -- Davis, E C -- Taylor, D G -- Boak, B B -- Wendel, D P -- K08 HL03490-03/HL/NHLBI NIH HHS/ -- T35 HL07744-06/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 1999 May 28;284(5419):1534-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Program in Human Molecular Biology and Genetics, Department of Human Genetics, Howard Hughes Medical Institute, University of Utah, Salt Lake City, UT 84112-5330, USA. dean.li@hci.utah.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10348742" target="_blank"〉PubMed〈/a〉
Schlagwort(e):
Animals
;
Antigens, CD
;
Antigens, CD31/analysis
;
Blood Vessels/cytology/*embryology/metabolism
;
Cell Differentiation
;
Crosses, Genetic
;
Endothelium, Vascular/cytology/*embryology/metabolism
;
Female
;
Gene Targeting
;
In Situ Hybridization
;
Male
;
Mice
;
Mice, Inbred C57BL
;
Microscopy, Electron
;
Muscle, Smooth, Vascular/cytology/*embryology
;
*Neovascularization, Physiologic
;
Receptors, Cell Surface
;
Signal Transduction
;
Transforming Growth Factor beta/metabolism
;
Vascular Cell Adhesion Molecule-1/genetics/*physiology
;
Yolk Sac/ultrastructure
Print ISSN:
0036-8075
Digitale ISSN:
1095-9203
Thema:
Biologie
,
Chemie und Pharmazie
,
Informatik
,
Medizin
,
Allgemeine Naturwissenschaft
,
Physik
Permalink