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- W2075996720 abstract "Channel catfish (Ictalurus punctatus) leukocyte immune-type receptors (IpLITRs) are immunoregulatory proteins belonging to the immunoglobulin superfamily that likely play an important role in the regulation of teleost immune cell effector responses. IpLITRs are expressed by myeloid and lymphoid subsets and based on their structural features can be classified as either putative stimulatory or inhibitory forms. We have recently demonstrated at the biochemical and functional levels that stimulatory IpLITR-types induced intracellular signaling cascades resulting in immune cell activation. Alternatively, we have shown that putative inhibitory IpLITRs may abrogate immune cell responses by recruiting teleost Src homology 2 (SH2) domain-containing cytoplasmic phosphatases (SHP) to their tyrosine-containing cytoplasmic tails. In the present study, we used vaccinia virus to express recombinant chimeric proteins encoding the extracellular and transmembrane regions of human KIR2DL3 fused with the cytoplasmic tails of two putative inhibitory IpLITRs (i.e. IpLITR1.2a and IpLITR1.1b) in mouse spleen-derived cytotoxic lymphocytes. This approach allowed us to study the specific effects of IpLITR-induced signaling on lymphocyte killing of B cell targets (e.g. 721.221 cells) using a standard chromium release assay. Our results suggest that both IpLITR1.2a and IpLITR1.1b are potent inhibitors of lymphocyte-mediated cellular cytotoxicity. Furthermore, using a catalytically inactive SHP-1 mutant in combination with site-directed mutagenesis and co-immunoprecipitations, we also demonstrate that the IpLITR1.2a-mediated functional inhibitory response is SHP-1-dependent. Alternatively, IpLITR1.1b-mediated inhibition of cellular cytotoxicity is facilitated by both SHP-1-dependent and independent mechanisms, possibly involving the C-terminal Src kinase (Csk). The involvement of this inhibitory kinase requires binding to a tyrosine residue encoded in the unique membrane proximal cytoplasmic tail region of IpLITR1.1b. Overall, this represents the first functional information for inhibitory IpLITR-types and reveals that catfish LITRs engage SHP-dependent and -independent inhibitory signaling pathways to abrogate lymphocyte-mediated killing." @default.
- W2075996720 created "2016-06-24" @default.
- W2075996720 creator A5041763221 @default.
- W2075996720 creator A5042841355 @default.
- W2075996720 creator A5050035445 @default.
- W2075996720 creator A5051835176 @default.
- W2075996720 date "2012-05-01" @default.
- W2075996720 modified "2023-10-04" @default.
- W2075996720 title "Channel catfish leukocyte immune-type receptor mediated inhibition of cellular cytotoxicity is facilitated by SHP-1-dependent and -independent mechanisms" @default.
- W2075996720 cites W1493742659 @default.
- W2075996720 cites W1494561978 @default.
- W2075996720 cites W1505599659 @default.
- W2075996720 cites W1513771042 @default.
- W2075996720 cites W1527352542 @default.
- W2075996720 cites W1541594543 @default.
- W2075996720 cites W1548078808 @default.
- W2075996720 cites W1548757245 @default.
- W2075996720 cites W1553517909 @default.
- W2075996720 cites W1790034387 @default.
- W2075996720 cites W1966930760 @default.
- W2075996720 cites W1969950463 @default.
- W2075996720 cites W1972178991 @default.
- W2075996720 cites W1974670739 @default.
- W2075996720 cites W1976805459 @default.
- W2075996720 cites W1977455794 @default.
- W2075996720 cites W1980823192 @default.
- W2075996720 cites W1981891742 @default.
- W2075996720 cites W1996058409 @default.
- W2075996720 cites W1999946772 @default.
- W2075996720 cites W2001324898 @default.
- W2075996720 cites W2014096863 @default.
- W2075996720 cites W2017504214 @default.
- W2075996720 cites W2017759565 @default.
- W2075996720 cites W2019420747 @default.
- W2075996720 cites W2019558661 @default.
- W2075996720 cites W2034408745 @default.
- W2075996720 cites W2035047005 @default.
- W2075996720 cites W2035555412 @default.
- W2075996720 cites W2036032819 @default.
- W2075996720 cites W2039998576 @default.
- W2075996720 cites W2042728577 @default.
- W2075996720 cites W2043094609 @default.
- W2075996720 cites W2045039830 @default.
- W2075996720 cites W2049360086 @default.
- W2075996720 cites W2052013741 @default.
- W2075996720 cites W2054366595 @default.
- W2075996720 cites W2055143049 @default.
- W2075996720 cites W2061097078 @default.
- W2075996720 cites W2063063012 @default.
- W2075996720 cites W2066969466 @default.
- W2075996720 cites W2070551124 @default.
- W2075996720 cites W2071724008 @default.
- W2075996720 cites W2073835145 @default.
- W2075996720 cites W2074852820 @default.
- W2075996720 cites W2075351740 @default.
- W2075996720 cites W2079057243 @default.
- W2075996720 cites W2083884970 @default.
- W2075996720 cites W2084466639 @default.
- W2075996720 cites W2086542713 @default.
- W2075996720 cites W2092328154 @default.
- W2075996720 cites W2098556757 @default.
- W2075996720 cites W2101257013 @default.
- W2075996720 cites W2101994976 @default.
- W2075996720 cites W2106756955 @default.
- W2075996720 cites W2110804196 @default.
- W2075996720 cites W2114453006 @default.
- W2075996720 cites W2118738797 @default.
- W2075996720 cites W2118740405 @default.
- W2075996720 cites W2123822428 @default.
- W2075996720 cites W2125488268 @default.
- W2075996720 cites W2130506153 @default.
- W2075996720 cites W2132268212 @default.
- W2075996720 cites W2133064156 @default.
- W2075996720 cites W2146573379 @default.
- W2075996720 cites W2152498364 @default.
- W2075996720 cites W2153578552 @default.
- W2075996720 cites W2158722170 @default.
- W2075996720 cites W2160675888 @default.
- W2075996720 cites W2167569919 @default.
- W2075996720 cites W2167634911 @default.
- W2075996720 cites W2168601978 @default.
- W2075996720 cites W2172180689 @default.
- W2075996720 cites W2325098089 @default.
- W2075996720 cites W2770627470 @default.
- W2075996720 cites W317592431 @default.
- W2075996720 cites W3186605366 @default.
- W2075996720 cites W4293168410 @default.
- W2075996720 doi "https://doi.org/10.1016/j.dci.2011.09.005" @default.
- W2075996720 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21945134" @default.
- W2075996720 hasPublicationYear "2012" @default.
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