Endomucin prevents leukocyte-endothelial cell adhesion and has a critical role under resting and inflammatory conditions.

نویسندگان

  • Alisar Zahr
  • Pilar Alcaide
  • Jinling Yang
  • Alexander Jones
  • Meredith Gregory
  • Nathaniel G dela Paz
  • Sunita Patel-Hett
  • Tania Nevers
  • Adarsha Koirala
  • Francis W Luscinskas
  • Magali Saint-Geniez
  • Bruce Ksander
  • Patricia A D'Amore
  • Pablo Argüeso
چکیده

Endomucin is a membrane-bound glycoprotein expressed luminally by endothelial cells that line postcapillary venules, a primary site of leukocyte recruitment during inflammation. Here we show that endomucin abrogation on quiescent endothelial cells enables neutrophils to adhere firmly, via LFA-1-mediated binding to ICAM-1 constitutively expressed by endothelial cells. Moreover, TNF-α stimulation downregulates cell surface expression of endomucin concurrent with increased expression of adhesion molecules. Adenovirus-mediated expression of endomucin under inflammatory conditions prevents neutrophil adhesion in vitro and reduces the infiltration of CD45(+) and NIMP-R14(+) cells in vivo. These results indicate that endomucin prevents leukocyte contact with adhesion molecules in non-inflamed tissues and that downregulation of endomucin is critical to facilitate adhesion of leukocytes into inflamed tissues.

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عنوان ژورنال:
  • Nature communications

دوره 7  شماره 

صفحات  -

تاریخ انتشار 2016