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Essential roles of SHPS-1 in induction of contact hypersensitivity of skin.

Motegi, Sei-Ichiro (författare)
Gunma University
Okazawa, Hideki (författare)
Gunma University
Murata, Yoji (författare)
Gunma University
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Kanazawa, Yoshitake (författare)
Gunma University
Saito, Yasuyuki (författare)
Gunma University
Kobayashi, Hisae (författare)
Gunma University
Ohnishi, Hiroshi (författare)
Gunma University
Oldenborg, Per-Arne (författare)
Umeå universitet,Histologi med cellbiologi
Ishikawa, Osamu (författare)
Gunma University
Matozaki, Takashi (författare)
Gunma University
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 (creator_code:org_t)
Elsevier BV, 2008
2008
Engelska.
Ingår i: Immunology Letters. - : Elsevier BV. - 0165-2478 .- 1879-0542. ; 121:1, s. 52-60
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • SHPS-1 is a transmembrane protein that binds the protein tyrosine phosphatases SHP-1 and SHP-2 and is abundant on the surface of CD11c(+) dendritic cells (DCs). We recently showed that SHPS-1 is essential for priming by DCs of CD4(+) T cells and for development of Th17 cell-mediated experimental autoimmunity. We have now further evaluated the importance of SHPS-1 and that of its ligand CD47 in contact hypersensitivity (CHS) to 2,4-dinitro-1-fluorobenzene (DNFB). Whereas the DNFB-induced CHS response was impaired in mice that express a mutant form of SHPS-1 lacking most of the cytoplasmic region, it was unaffected in CD47-deficient mice. Moreover, treatment of wild-type mice with mAbs to SHPS-1 that either block or do not block the binding of SHPS-1 to CD47 inhibited the CHS response. A mAb to CD47 had no such effect. The 2,4-dinitro-benzenesulfonic acid-induced proliferation of, and production of IFN-gamma or IL-17 by, T cells from DNFB-sensitized wild-type mice were inhibited by either mAb to SHPS-1 but not by that to CD47. In contrast, the blocking mAbs to SHPS-1, but not that to CD47, inhibited an allogeneic mixed leukocyte reaction. Both mAbs to SHPS-1, but not that to CD47, also inhibited the lipopolysaccharide- or polyinosinic-polycytidylic acid-induced production of TNF-alpha by DCs. These results suggest that SHPS-1 is essential for development of CHS, likely as a result of its positive regulation of the priming by DCs of CD4(+) T cells. However, such regulation by SHPS-1 does not appear to require its interaction with CD47.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine (hsv//eng)

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