帕尔瓦布明
DLX5型
神经节隆起
钙黄绿素
中间神经元
神经科学
生物
同源盒
大脑
中枢神经系统
基因表达
抑制性突触后电位
基因
生物化学
免疫学
免疫组织化学
作者
Yanling Wang,Catherine A. Dye,Vikaas S. Sohal,Jason E. Long,Rosanne C. Estrada,Tomas Roztocil,Thomas Lufkin,Karl Deisseroth,Scott C. Baraban,John L.R. Rubenstein
标识
DOI:10.1523/jneurosci.5963-09.2010
摘要
Dlx5 and Dlx6 homeobox genes are expressed in developing and mature cortical interneurons. Simultaneous deletion of Dlx5 and 6 results in exencephaly of the anterior brain; despite this defect, prenatal basal ganglia differentiation appeared largely intact, while tangential migration of Lhx6 + and Mafb + interneurons to the cortex was reduced and disordered. The migration deficits were associated with reduced CXCR4 expression. Transplantation of mutant immature interneurons into a wild-type brain demonstrated that loss of either Dlx5 or Dlx5&6 preferentially reduced the number of mature parvalbumin + interneurons; those parvalbumin + interneurons that were present had increased dendritic branching. Dlx5 /6 +/− mice, which appear normal histologically, show spontaneous electrographic seizures and reduced power of gamma oscillations. Thus, Dlx5&6 appeared to be required for development and function of somal innervating (parvalbumin + ) neocortical interneurons. This contrasts with Dlx1 , whose function is required for dendrite innervating (calretinin + , somatostatin + , and neuropeptide Y + ) interneurons (Cobos et al., 2005).
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