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      Girdin Is an Intrinsic Regulator of Neuroblast Chain Migration in the Rostral Migratory Stream of the Postnatal Brain

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          Abstract

          In postnatally developing and adult brains, interneurons of the olfactory bulb (OB) are continuously generated at the subventricular zone of the forebrain. The newborn neuroblasts migrate tangentially to the OB through a well defined pathway, the rostral migratory stream (RMS), where the neuroblasts undergo collective migration termed “chain migration.” The cell-intrinsic regulatory mechanism of neuroblast chain migration, however, has not been uncovered. Here we show that mice lacking the actin-binding Akt substrate Girdin (a protein that interacts with Disrupted-In-Schizophrenia 1 to regulate neurogenesis in the dentate gyrus) have profound defects in neuroblast chain migration along the RMS. Analysis of two gene knock-in mice harboring Girdin mutants identified unique amino acid residues in Girdin's C-terminal domain that are responsible for the regulation of neuroblast chain migration but revealed no apparent requirement of Girdin phosphorylation by Akt. Electron microscopic analyses demonstrated the involvement of Girdin in neuroblast cell–cell interactions. These findings suggest that Girdin is an important intrinsic factor that specifically governs neuroblast chain migration along the RMS.

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          Author and article information

          Journal
          J Neurosci
          J. Neurosci
          jneuro
          jneurosci
          J. Neurosci
          The Journal of Neuroscience
          Society for Neuroscience
          0270-6474
          1529-2401
          1 June 2011
          : 31
          : 22
          : 8109-8122
          Affiliations
          [1] 1Departments of Pathology and
          [2] 2Cell Pharmacology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan,
          [3] 3Department of Developmental and Regenerative Biology, Institute of Molecular Medicine, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan,
          [4] 4Institute for Advanced Research, Nagoya University, Nagoya 464-8601, Japan,
          [5] 5Core Research for Evolutionary Science and Technology, Japan Science and Technology Agency, Saitama 332-0012, Japan, and
          [6] 6Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205
          Author notes
          Correspondence should be addressed to Masahide Takahashi, Department of Pathology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan. mtakaha@ 123456med.nagoya-u.ac.jp

          Author contributions: Y.W., N.K., N.A., A.E., K.S., and M.T. designed research; Y.W., N.K., N.A., A.E., M.I.-S., T.K., M.A., Y.M., H.O., T.H., T.N., and K. Ku. performed research; K. Ka., G.-l.M., H.S., and K.S. contributed unpublished reagents/analytic tools; Y.W., N.A., A.E., and M.T. wrote the paper.

          *Y.W., N.K., and N.A. contributed equally to this work.

          Article
          PMC5491307 PMC5491307 5491307 3699212
          10.1523/JNEUROSCI.1130-11.2011
          5491307
          21632933
          9fa0224c-69ad-4754-bfd7-3fb5905de8a5
          Copyright © 2011 the authors 0270-6474/11/318109-14$15.00/0
          History
          : 3 March 2011
          : 14 April 2011
          : 15 April 2011
          Categories
          Articles
          Development/Plasticity/Repair

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