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• W1966770149 abstract "Semaphorins are a large family of secreted and membrane-bound proteins. Recently, several roles of semaphorins in the immune system have emerged. Several semaphorins and their receptors are expressed in a variety of lymphoid and myeloid cells and affect immune cell functions, including cell proliferation, differentiation, chemotaxis, and cytokine production. However, the roles of class 3 semaphorins in human myeloid cells are not well known. Here we examined the regulation of expression of class 3 semaphorins and their receptors by inflammatory stimuli and their function in human macrophages. We show that the expression of Sema3A receptors (neuropilin-1 (NRP-1), NRP-2, plexin A1, plexin A2, and plexin A3) significantly increased during M-CSF-mediated differentiation of monocytes into macrophages under conditions that promote an M2 alternatively activated macrophage phenotype. Consistent with increased NRP-1 expression, cell surface binding of Sema3A increased during M2 differentiation. Interferon (IFN)-gamma and lipopolysaccharide, which promote classical M1 macrophage activation affected expression of NRP-1, NRP-2 and plexin A1. IFN-gamma decreased NRP-1 expression and LPS suppressed NRP-2 and plexin A1 expression. Furthermore we show that Sema3A induced apoptosis in monocyte-derived macrophages and cooperated with anti-Fas CH11 antibody to augment apoptosis. Our results suggest that Sema3A plays a role in induction of apoptosis in monocyte-derived macrophages that are resistant to Fas-induced apoptosis, and that its function can be modulated in inflammatory conditions." @default.
• W1966770149 created "2016-06-24" @default.
• W1966770149 creator A5059931993 @default.
• W1966770149 creator A5084611630 @default.
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• W1966770149 date "2009-04-01" @default.
• W1966770149 modified "2023-10-11" @default.
• W1966770149 title "Expression and function of semaphorin 3A and its receptors in human monocyte-derived macrophages" @default.
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• W1966770149 doi "https://doi.org/10.1016/j.humimm.2009.01.026" @default.
• W1966770149 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4811352" @default.
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