Stromal derived factor-1 exerts differential regulation on distinct cortical cell populations in vitro

James Pritchett, Clare Wright, Leo Zeef, Bagirathy Nadarajah

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Background. Stromal derived factor (SDF-1), an alpha chemokine, is a widely known chemoattractant in the immune system. A growing body of evidence now suggests multiple regulatory roles for SDF-1 in the developing nervous system. Results. To investigate the role of SDF-1 signaling in the growth and differentiation of cortical cells, we performed numerous in vitro experiments, including gene chip and quantitative RT-PCR analysis. Using SDF-1 medium and AMD3100, a receptor antagonist, we demonstrate that the chemokine signaling regulates key events during early cortical development. First, SDF-1 signaling maintains cortical progenitors in proliferation, possibly through a mechanism involving connexin 43 mediated intercellular coupling. Second, SDF-1 signaling upregulates the differentiation of cortical GABAergic neurons, independent of sonic signaling pathway. Third, SDF-1 enables the elongation and branching of axons of cortical glutamatergic neurons. Finally, cortical cultures derived from CXCR4-/- mutants show a close parallel to AMD3100 treatment with reduced cell proliferation and differentiation of GABAergic neurons. Conclusion. Results from this study show that SDF-1 regulates distinct cortical cell populations in vitro. © 2007 Pritchett et al; licensee BioMed Central Ltd.
    Original languageEnglish
    Article number31
    JournalBMC Developmental Biology
    Volume7
    DOIs
    Publication statusPublished - 2007

    Keywords

    • Animals
    • ultrastructure: Axons
    • Cell Differentiation
    • Cell Proliferation
    • Cells, Cultured
    • cytology: Cerebral Cortex
    • genetics: Chemokines, CXC
    • Culture Media, Conditioned
    • Enzyme-Linked Immunosorbent Assay
    • Gene Expression Regulation, Developmental
    • Immunohistochemistry
    • Mice
    • Mutation
    • cytology: Neurons
    • Oligonucleotide Array Sequence Analysis
    • Rats
    • genetics: Receptors, CXCR4
    • Reverse Transcriptase Polymerase Chain Reaction

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