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. 2016 Jan 20;61(15):1935–1945. doi: 10.1007/s00018-004-4137-5

Differential chemotactic potential of mouse platelet basic protein for thymocyte subsets

W X Fu 1, S Y Gong 1, X P Qian 1, Y Li 1, M L Zhu 1, X Y Dong 1, Y Li 1, W F Chen 1,
PMCID: PMC11138683  PMID: 15289935

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/Mφs). Recombinant mPBP was chemoattractive for target cells of polymorphonuclear leucocytes, peritoneal Mo/Mφs 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/Mφs can produce mPBP implies that they may have other functions apart from acting as scavengers in thymus.

Keywords: Chemokine, chemotaxis, monocyte/macrophage, stromal cell, thymus

Footnotes

Received 25 March 2004; received after revision 10 May 2004; accepted 8 June 2004


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