Membrane-associated CD93 regulates leukocyte migration and C1q-hemolytic activity during murine peritonitis

Mallary C. Greenlee-Wacker, Carlos Briseño, Manuel Galvan, Gabriela Moriel, Peter Velázquez, Suzanne S. Bohlson

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20 Scopus citations


CD93 is emerging as a novel regulator of inflammation; however, its molecular function is unknown. CD93 exists as a membraneassociated glycoprotein on the surface of cells involved in the inflammatory cascade, including endothelial and myeloid cells. A soluble form (sCD93) is detectable in blood and is elevated with inflammation. In this study, we demonstrate heightened susceptibility to thioglycollate-induced peritonitis in CD93-/- mice. CD93-/- mice showed a 1.6-1.8-fold increase in leukocyte infiltration during thioglycollate-induced peritonitis between 3 and 24 h that returned to wild type levels by 96 h. Impaired vascular integrity in CD93 -/- mice during peritonitis was demonstrated using fluorescence multiphoton intravital microscopy; however, no differences in cytokine or chemokine levels were detected with Luminex Multiplex or ELISA analysis. C1q-hemolytic activity in CD93-/-mice was decreased by 22% at time zero and by 46% 3 h after thioglycollate injection, suggesting a defect in the classical complement pathway. Leukocyte recruitment and C1q-hemolytic activity was restored to wild type levels when CD93 was expressed on either hematopoietic cells or nonhematopoietic cells in bone marrow chimeric mice. However, elevated levels of sCD93 in inflammatory fluid were observed only when CD93 was expressed on nonhematopoietic cells. Because cell-associated CD93 was sufficient to restore a normal inflammatory response, these data suggest that cell-associated CD93, and not sCD93, regulates leukocyte recruitment and complement activation during murine peritonitis.

Original languageEnglish
Pages (from-to)3353-3361
Number of pages9
JournalJournal of Immunology
Issue number6
StatePublished - Sep 15 2011


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