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Development ; 128(11): 1971-81, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11493520

ABSTRACT

The chemokine SDF-1 alpha (CXC12) and its receptor CXCR4 have been shown to play a role in the development of normal cerebellar cytoarchitecture. We report here that SDF-1 alpha both induces chemotactic responses in granule precursor cells and enhances granule cell proliferative responses to Sonic hedgehog. Chemotactic and proliferative responses to SDF-1 alpha are greater in granule cells obtained from cerebella of animals in the first postnatal week, coinciding with the observed in vivo peak in cerebellar CXCR4 expression. SDF-1 alpha activation of neuronal CXCR4 differs from activation of CXCR4 in leukocytes in that SDF-1 alpha-induced calcium flux is activity dependent, requiring predepolarization with KCl or pretreatment with glutamate. However, as is the case in leukocytes, neuronal responses to SDF-1 alpha are all abolished by pretreatment of granule cells with pertussis toxin, suggesting they occur through G(alpha i) activation. In conclusion, SDF-1 alpha plays a role in two important processes of granule cell maturation - proliferation and migration - assisting in the achievement of appropriate cell number and position in the cerebellar cortex.


Subject(s)
Cerebellum/cytology , Chemokines, CXC/physiology , Chemotaxis/physiology , Trans-Activators/physiology , Animals , Calcium/metabolism , Cell Division , Cell Polarity , Cerebellum/metabolism , Chemokine CXCL12 , Chemokines, CXC/genetics , Chemokines, CXC/metabolism , Female , Hedgehog Proteins , Male , Mice , Mice, Inbred BALB C , Rats , Receptors, CXCR4/genetics , Trans-Activators/metabolism
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