Aberrant differentiation of glutamatergic cells in neocortex of mouse model for fragile X syndrome

Topi A Tervonen, Verna Louhivuori, Xiaohong Sun, Marie-Estelle Hokkanen, Claudius F Kratochwil, Pawel Zebryk, Eero Castren, Maija Castren

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Sammanfattning

The lack of fragile X mental retardation protein (FMRP) causes fragile X syndrome, a common form of inherited mental retardation. Our previous studies revealed alterations in the differentiation of FMRP-deficient neural progenitors. Here, we show abnormalities in neurogenesis in the mouse and human embryonic FMRP-deficient brain as well as after in utero transfection of 1304N mutated FMRP, which acts in a dominant negative manner in the wild-type mouse brain. Progenitors accumulated abnormally in the subventricular zone of the embryonic Fmr1-knockout (Fmr1-KO) mouse neocortex. An increased density of cells expressing sequentially an intermediate progenitor marker, T-box transcription factor (Tbr2), and a postmitotic neuron marker, T-brain 1 (Tbr1), indicated that the differentiation to glutamatergic cell lineages was particularly disturbed. These abnormalities were associated with an increased density of pyramidal cells of the layer V in the early postnatal neocortex suggesting a role for FMRP in the regulation of the differentiation of neocortical glutamatergic neurons. (C) 2008 Elsevier Inc. All rights reserved.
Originalspråkengelska
TidskriftNeurobiology of Disease
Volym33
Utgåva2
Sidor (från-till)250-259
Antal sidor10
ISSN0969-9961
DOI
StatusPublicerad - 2009
MoE-publikationstypA1 Tidskriftsartikel-refererad

Vetenskapsgrenar

  • 311 Basmedicin
  • 118 Biovetenskaper
  • 515 Psykologi

Citera det här