Carcinoembryonic antigen‐related cell adhesion molecule‐1 (CEACAM1) is known to be crucial to vasculogenesis and angiogenesis. Recently, CEACAM1 deficiency was shown to result in the formation of aortic plaque‐like lesions, indicating a role for...
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https://www.riss.kr/link?id=O120814872
2018년
-
0892-6638
1530-6860
SCI;SCIE;SCOPUS
학술저널
5612-5625 [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
Carcinoembryonic antigen‐related cell adhesion molecule‐1 (CEACAM1) is known to be crucial to vasculogenesis and angiogenesis. Recently, CEACAM1 deficiency was shown to result in the formation of aortic plaque‐like lesions, indicating a role for...
Carcinoembryonic antigen‐related cell adhesion molecule‐1 (CEACAM1) is known to be crucial to vasculogenesis and angiogenesis. Recently, CEACAM1 deficiency was shown to result in the formation of aortic plaque‐like lesions, indicating a role for CEACAM1 in adult vessels as well. The underlying mechanisms remained largely elusive. Therefore, we aimed to elucidate the role of CEACAM1 in endothelial homeostasis. Here, we show that CEACAM1 deficiency causes subcellular eNOS redistribution in endothelial cells (i.e., by eNOS depalmitoylation) and alters endothelial glycocalyx that confers antiadhesive properties to the endothelium (i.e., by repression of glycocalyx‐degrading enzymes). Accordingly, our analysis revealed an increased leukocyte‐endothelial interaction in CEACAM1‐deficient endothelium. In addition, CEACAM1 age dependently modulated basal and TNF‐α‐mediated endothelial barrier (EB) leakiness. In younger mice, CEACAM1 was protective for EB, whereas in aged mice it promoted EB leakiness. EB function depends on interendothelial adherence junctions formed by β‐catenin/vascular endothelial‐cadherin complexes. We show here that CEACAM1 influenced basal and TNF‐α‐mediated phosphorylation of β‐catenin and caveolin‐1, which are essential players in EB modulation. Both increased adhesiveness to leukocytes and EB modulation due to CEACAM1 deficiency may facilitate inflammatory cell transmigration into the vascular wall and subsequent plaque formation. Collectively, these results identify a crucial role for CEACAM1 in endothelial homeostasis of adult blood vessels.—Ghavampour, S., Kleefeldt, F., Bömmel, H., Volland, J., Paus, A., Horst, A., Pfeiffer, V., Hübner, S., Wagner, N., Rueckschloss, U., Ergün, S. Endothelial barrier function is differentially regulated by CEACAM1‐ mediated signaling. FASEB J. 32, 5612–5625 (2018). www.fasebj.org
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