74
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      The Indispensable Roles of Microglia and Astrocytes during Brain Development

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Glia are essential for brain functioning during development and in the adult brain. Here, we discuss the various roles of both microglia and astrocytes, and their interactions during brain development. Although both cells are fundamentally different in origin and function, they often affect the same developmental processes such as neuro-/gliogenesis, angiogenesis, axonal outgrowth, synaptogenesis and synaptic pruning. Due to their important instructive roles in these processes, dysfunction of microglia or astrocytes during brain development could contribute to neurodevelopmental disorders and potentially even late-onset neuropathology. A better understanding of the origin, differentiation process and developmental functions of microglia and astrocytes will help to fully appreciate their role both in the developing as well as in the adult brain, in health and disease.

          Related collections

          Most cited references427

          • Record: found
          • Abstract: found
          • Article: not found

          Fate mapping analysis reveals that adult microglia derive from primitive macrophages.

          Microglia are the resident macrophages of the central nervous system and are associated with the pathogenesis of many neurodegenerative and brain inflammatory diseases; however, the origin of adult microglia remains controversial. We show that postnatal hematopoietic progenitors do not significantly contribute to microglia homeostasis in the adult brain. In contrast to many macrophage populations, we show that microglia develop in mice that lack colony stimulating factor-1 (CSF-1) but are absent in CSF-1 receptor-deficient mice. In vivo lineage tracing studies established that adult microglia derive from primitive myeloid progenitors that arise before embryonic day 8. These results identify microglia as an ontogenically distinct population in the mononuclear phagocyte system and have implications for the use of embryonically derived microglial progenitors for the treatment of various brain disorders.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo.

            Microglial cells represent the immune system of the mammalian brain and therefore are critically involved in various injuries and diseases. Little is known about their role in the healthy brain and their immediate reaction to brain damage. By using in vivo two-photon imaging in neocortex, we found that microglial cells are highly active in their presumed resting state, continually surveying their microenvironment with extremely motile processes and protrusions. Furthermore, blood-brain barrier disruption provoked immediate and focal activation of microglia, switching their behavior from patroling to shielding of the injured site. Microglia thus are busy and vigilant housekeepers in the adult brain.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Synaptic pruning by microglia is necessary for normal brain development.

              Microglia are highly motile phagocytic cells that infiltrate and take up residence in the developing brain, where they are thought to provide a surveillance and scavenging function. However, although microglia have been shown to engulf and clear damaged cellular debris after brain insult, it remains less clear what role microglia play in the uninjured brain. Here, we show that microglia actively engulf synaptic material and play a major role in synaptic pruning during postnatal development in mice. These findings link microglia surveillance to synaptic maturation and suggest that deficits in microglia function may contribute to synaptic abnormalities seen in some neurodevelopmental disorders.
                Bookmark

                Author and article information

                Contributors
                Journal
                Front Hum Neurosci
                Front Hum Neurosci
                Front. Hum. Neurosci.
                Frontiers in Human Neuroscience
                Frontiers Media S.A.
                1662-5161
                08 November 2016
                2016
                : 10
                : 566
                Affiliations
                [1] 1Swammerdam Institute for Life Sciences, University of Amsterdam Amsterdam, Netherlands
                [2] 2Department of Psychiatry and Behavioral Sciences, UC Davis MIND Institute Sacramento, CA, USA
                [3] 3Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht Utrecht, Netherlands
                [4] 4Netherlands Institute for Neuroscience Amsterdam, Netherlands
                Author notes

                Edited by: Rajeev Krishnadas, NHS Greater Glasgow and Clyde, UK

                Reviewed by: Yvonne Nolan, University College Cork, Ireland; Amanda Sierra, Achucarro Basque Center for Neuroscience, Spain

                *Correspondence: Paul J. Lucassen p.j.lucassen@ 123456uva.nl

                Shared senior authorship.

                Article
                10.3389/fnhum.2016.00566
                5099170
                27877121
                3b6204ef-3234-4e24-a56c-7566b6c43ede
                Copyright © 2016 Reemst, Noctor, Lucassen and Hol.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 22 June 2016
                : 25 October 2016
                Page count
                Figures: 3, Tables: 1, Equations: 0, References: 400, Pages: 28, Words: 25523
                Funding
                Funded by: Nederlandse Organisatie voor Wetenschappelijk Onderzoek 10.13039/501100003246
                Funded by: ZonMw 10.13039/501100001826
                Categories
                Neuroscience
                Review

                Neurosciences
                microglia,astrocytes,brain development,glial cells,neurodevelopmental disorders
                Neurosciences
                microglia, astrocytes, brain development, glial cells, neurodevelopmental disorders

                Comments

                Comment on this article