The MHP36 line of murine neural stem cells expresses functional CXCR1 chemokine receptors that initiate chemotaxis in vitro

被引:11
作者
Beech, John Samuel
Wheeler, Daniel Wren
Reckless, Jill
Grant, Andrew James
Price, Jack
Mastroeni, Pietro
Grainger, David John
Menon, David Krishna
机构
[1] Univ Cambridge, Addenbrookes Hosp, Div Anaesthesia, Cambridge CB2 2QQ, England
[2] Univ Cambridge, Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, England
[3] Univ Cambridge, Dept Clin Vet Med, Cambridge CB3 0ES, England
[4] Inst Psychiat, Kings Coll, London SE5 8AF, England
基金
英国医学研究理事会;
关键词
neural stem cells; chemokines; receptors; chemokine; interleukin-8A; interleukin-8; chemotaxis;
D O I
10.1016/j.jneuroim.2006.12.015
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chemokines help to establish cerebral inflammation after ischemia, which comprises a major component of secondary brain injury. The CXCR4 chemokine receptor system induces neural stem cell migration, and hence has been implicated in brain repair. We show that CXCR1 and interleukin-8 also stimulate chemotaxis in murine neural stem cells from the MHP36 cell line. The presence of CXCR1 was confirmed by reverse transcriptase PCR and immunohistochemistry. Interleukin-8 evoked intracellular calcium currents, upregulated doublecortin (a protein expressed by migrating neuroblasts), and elicited positive chemotaxis in vitro. Therefore, effectors of the early innate immune response may also influence brain repair mechanisms. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:198 / 208
页数:11
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