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Differential chemotactic potential of mouse platelet basic protein for thymocyte subsets
Authors:W.?X.?Fu,S.?Y.?Gong,X.?P.?Qian,Y.?Li,M.?L.?Zhu,X.?Y.?Dong,Y.?Li,W.?F.?Chen  author-information"  >  author-information__contact u-icon-before"  >  mailto:wfchen@public.bta.net.cn"   title="  wfchen@public.bta.net.cn"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Department of Immunology, Peking University Health Science Center, 100083 Beijing, China
Abstract:Mouse platelet basic protein (CXCL7/mPBP) was cloned from thymic stromal cells and further identification indicated that it was expressed in thymic monocytes/macrophages (Mo/Mphgrs). Recombinant mPBP was chemoattractive for target cells of polymorphonuclear leucocytes, peritoneal Mo/Mphgrs and splenic lymphocytes with distinct potencies. CXCR2 was identified to be a cognate receptor for mPBP. Mouse thymocyte subsets of CD4-CD8- double-negative (DN), CD4+CD8+ double-positive (DP), CD4+CD8- single-positive (CD4SP) and CD4-CD8+ single-positive (CD8SP) expressed cell surface CXCR2 with different positive percentages and expression levels. mPBP was chemoattractive for thymocyte subsets with the potency order DN>DP> CD8SP>CD4SP, consistent with the levels of CXCR2 expressed on the respective cells. Thus, mPBP in thymus is functionally redundant with chemokine CXCL12/ SDF-1. Moreover, our finding that thymic Mo/Mphgrs can produce mPBP implies that they may have other functions apart from acting as scavengers in thymus.Received 25 March 2004; received after revision 10 May 2004; accepted 8 June 2004
Keywords:Chemokine  chemotaxis  monocyte/macrophage  stromal cell  thymus
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