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J Neuroimmunol ; 184(1-2): 198-208, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17289163

ABSTRACT

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.


Subject(s)
Chemotaxis/physiology , Gene Expression/physiology , Neurons/metabolism , Receptors, Interleukin-8A/metabolism , Stem Cells/metabolism , Analysis of Variance , Animals , Calcium/metabolism , Cell Line , Cell Movement/drug effects , Cell Movement/physiology , Chemotaxis/drug effects , Dose-Response Relationship, Drug , Doublecortin Domain Proteins , Drug Interactions , Enzyme Inhibitors/pharmacology , Flow Cytometry/methods , Gene Expression/drug effects , Immunohistochemistry/methods , In Vitro Techniques , Interleukin-8/pharmacology , Mice , Microtubule-Associated Proteins/metabolism , Neurons/drug effects , Neuropeptides/metabolism , Peptides, Cyclic/pharmacology , RNA, Messenger/biosynthesis , Receptors, Interleukin-8A/genetics , Reverse Transcriptase Polymerase Chain Reaction/methods , Stem Cells/drug effects
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