Identification of CSF-1 as a brain macrophage migratory activity produced by astrocytes
Autor: | Michel Mallat, Charles-Félix Calvo, Jacques Glowinski, Michèle Gelman, Alexandre Dobbertin |
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Rok vydání: | 1998 |
Předmět: |
Cell Survival
medicine.medical_treatment Central nervous system Enzyme-Linked Immunosorbent Assay Biology Cellular and Molecular Neuroscience Cell Movement medicine Animals Humans Macrophage Cells Cultured Brain Chemistry Neurons Microglia Macrophage Colony-Stimulating Factor Macrophages Brain Blotting Northern Rats Cell biology Chemotaxis Leukocyte medicine.anatomical_structure Cytokine Neurology Cerebral cortex Astrocytes Immunology Cytokines Neuroglia Cell Division Chemotaxis assay Astrocyte |
Zdroj: | Glia. 24:180-186 |
ISSN: | 1098-1136 0894-1491 |
Popis: | Intraparenchymal migration of macrophages occurs in the CNS during development or as a consequence of tissue injuries. In the present study, we have shown, by using an in vitro chemotaxis assay, that cultured rat astrocytes obtained from the developing cerebral cortex and striatum produce soluble factors, which attract purified brain macrophages. The effect of astrocyte-derived factors on macrophages was strongly reduced in the presence of antibodies neutralizing colony-stimulating factor 1 (CSF-1, also called M-CSF), and recombinant CSF-1 was found to act as a chemotactic agent on brain macrophages. Synthesis of CSF-1 by cultured astrocytes was confirmed by northern detection of CSF-1 transcripts. In contrast, the CSF-1 gene was not expressed by cultured neurons from the cerebral cortex and striatum or by the brain macrophage population responsive to CSF-1 gradient. ELISA detection of CSF-1 in tissue extracts revealed the occurrence of this cytokine in the rat cerebral cortex during postnatal development and in adults. Altogether, our results demonstrate that astrocytes, through CSF-1 secretion, can trigger the polarized migration of brain macrophages and suggest a new mechanism which could regulate the locomotion of these cells in the cerebral cortex during ontogenesis or following lesions. |
Databáze: | OpenAIRE |
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