Literature DB >> 21305616

Pattern of invasion of the embryonic mouse spinal cord by microglial cells at the time of the onset of functional neuronal networks.

C Rigato1, R Buckinx, H Le-Corronc, J M Rigo, P Legendre.   

Abstract

Microglial cells invade the central nervous system during embryonic development, but their developmental functional roles in vivo remain largely unknown. Accordingly, their invasion pattern during early embryonic development is still poorly understood. To address this issue, we analyzed the initial developmental pattern of microglial cell invasion in the spinal cord of CX3CR1-eGFP mouse embryos using immunohistochemistry. Microglial cells began to invade the mouse embryonic spinal cord at a developmental period corresponding to the onset of spontaneous electrical activity and of synaptogenesis. Microglial cells reached the spinal cord through the peripheral vasculature and began to invade the parenchyma at 11.5 days of embryonic age (E11.5). Remarkably, at E12.5, activated microglial cells aggregated in the dorsolateral region close to terminals of dying dorsal root ganglia neurons. At E13.5, microglial cells in the ventral marginal zone interacted with radial glial cells, whereas ramified microglial cells within the parenchyma interacted with growing capillaries. At this age, activated microglial cells (Mac-2 staining) also accumulated within the lateral motor columns at the onset of the developmental cell death of motoneurons. This cell aggregation was still observed at E14.5, but microglial cells no longer expressed Mac-2. At E15.5, microglial cells were randomly distributed within the parenchyma. Our results provide the essential basis for further studies on the role of microglial cells in the early development of spinal cord neuronal networks in vivo.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21305616     DOI: 10.1002/glia.21140

Source DB:  PubMed          Journal:  Glia        ISSN: 0894-1491            Impact factor:   7.452


  40 in total

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Review 4.  Fine-tuning the central nervous system: microglial modelling of cells and synapses.

Authors:  Anna L Xavier; João R L Menezes; Steven A Goldman; Maiken Nedergaard
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2014-10-19       Impact factor: 6.237

5.  N-terminal horseshoe conformation of DCC is functionally required for axon guidance and might be shared by other neural receptors.

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6.  Developmental changes in microglial mobilization are independent of apoptosis in the neonatal mouse hippocampus.

Authors:  Ukpong B Eyo; Samuel A Miner; Joshua A Weiner; Michael E Dailey
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Review 7.  Innate immune activation in neurodegenerative disease.

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8.  Characterization of inflammatory gene expression and galectin-3 function after spinal cord injury in mice.

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Review 9.  Microglia: key elements in neural development, plasticity, and pathology.

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Journal:  J Neuroimmune Pharmacol       Date:  2013-01-27       Impact factor: 4.147

10.  Microglia proliferation is controlled by P2X7 receptors in a Pannexin-1-independent manner during early embryonic spinal cord invasion.

Authors:  Chiara Rigato; Nina Swinnen; Roeland Buckinx; Isabelle Couillin; Jean-Marie Mangin; Jean-Michel Rigo; Pascal Legendre; Hervé Le Corronc
Journal:  J Neurosci       Date:  2012-08-22       Impact factor: 6.167

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