Polysialyltransferase expression is linked to neuronal migration in the developing and adult zebrafish

Dev Dyn. 2008 Jan;237(1):276-85. doi: 10.1002/dvdy.21410.

Abstract

Modulation of cell-cell adhesion is crucial for regulating neuronal migration and maintenance of structural plasticity in the embryonic and mature brain. Such modulation can be obtained by the enzymatic attachment of polysialic acid (PSA) to the neural cell adhesion molecule (NCAM) by means of the polysialyltransferases STX and PST. Thus, differential expression of STX and PST is likely to be responsible for varying functions of PSA-NCAM during neuronal differentiation, maintenance, plasticity, and regeneration. We have isolated the zebrafish homologues of STX (St8sia2) and PST (St8sia4) and demonstrate that their expression in the embryonic and adult nervous system is often confined to regions of neuronal migration. Moreover, in the adult cerebellum, the complementary expression pattern of both polysialyltransferases suggests a function in regulating cerebellar neuronal plasticity. Enzymatic removal of PSA in the embryonic cerebellum results in impaired neuronal migration, suggesting that PSA-NCAM is a key regulator of motility for cerebellar neuronal progenitors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / embryology
  • Brain / growth & development
  • Brain / metabolism
  • Cell Adhesion / genetics
  • Cell Adhesion / physiology
  • Cell Movement / genetics*
  • Cell Movement / physiology
  • Central Nervous System / embryology
  • Central Nervous System / growth & development
  • Central Nervous System / metabolism
  • Cerebellum / embryology
  • Cerebellum / growth & development
  • Cerebellum / metabolism
  • Gene Expression Regulation, Developmental
  • Immunohistochemistry
  • Neural Cell Adhesion Molecules / genetics
  • Neural Cell Adhesion Molecules / metabolism
  • Neural Cell Adhesion Molecules / physiology
  • Neurons / cytology
  • Neurons / enzymology
  • Neurons / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sialic Acids / metabolism
  • Sialyltransferases / genetics*
  • Sialyltransferases / metabolism
  • Zebrafish / embryology
  • Zebrafish / genetics*
  • Zebrafish / growth & development
  • Zebrafish Proteins / genetics*
  • Zebrafish Proteins / metabolism
  • Zebrafish Proteins / physiology

Substances

  • Neural Cell Adhesion Molecules
  • Sialic Acids
  • Zebrafish Proteins
  • ncam1a protein, zebrafish
  • polysialic acid
  • CMP-N-acetylneuraminate-poly-alpha-2,8-sialosyl sialyltransferase
  • Sialyltransferases