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 language | English |
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Article number | 31 |
Journal | BMC Developmental Biology |
Volume | 7 |
DOIs | |
Publication status | Published - 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