| Literature DB >> 26231120 |
Anna Bunin1, Vanja Sisirak2, Hiyaa S Ghosh3, Lucja T Grajkowska2, Z Esther Hou3, Michelle Miron3, Cliff Yang3, Michele Ceribelli4, Noriko Uetani5, Laurence Chaperot6, Joel Plumas6, Wiljan Hendriks7, Michel L Tremblay5, Hans Häcker8, Louis M Staudt4, Peter H Green9, Govind Bhagat10, Boris Reizis11.
Abstract
Plasmacytoid dendritic cells (pDCs) are primary producers of type I interferon (IFN) in response to viruses. The IFN-producing capacity of pDCs is regulated by specific inhibitory receptors, yet none of the known receptors are conserved in evolution. We report that within the human immune system, receptor protein tyrosine phosphatase sigma (PTPRS) is expressed specifically on pDCs. Surface PTPRS was rapidly downregulated after pDC activation, and only PTPRS(-) pDCs produced IFN-α. Antibody-mediated PTPRS crosslinking inhibited pDC activation, whereas PTPRS knockdown enhanced IFN response in a pDC cell line. Similarly, murine Ptprs and the homologous receptor phosphatase Ptprf were specifically co-expressed in murine pDCs. Haplodeficiency or DC-specific deletion of Ptprs on Ptprf-deficient background were associated with enhanced IFN response of pDCs, leukocyte infiltration in the intestine and mild colitis. Thus, PTPRS represents an evolutionarily conserved pDC-specific inhibitory receptor, and is required to prevent spontaneous IFN production and immune-mediated intestinal inflammation.Entities:
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Year: 2015 PMID: 26231120 PMCID: PMC4547994 DOI: 10.1016/j.immuni.2015.07.009
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745