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DLX - 2、MASH - 1和MAP - 2的表达以及溴脱氧尿苷掺入确定了胚胎小鼠前脑中分子层面不同的细胞群。

DLX-2, MASH-1, and MAP-2 expression and bromodeoxyuridine incorporation define molecularly distinct cell populations in the embryonic mouse forebrain.

作者信息

Porteus M H, Bulfone A, Liu J K, Puelles L, Lo L C, Rubenstein J L

机构信息

Nina Ireland Laboratory of Developmental Biology, Department of Psychiatry, University of California, San Francisco 94143-0984.

出版信息

J Neurosci. 1994 Nov;14(11 Pt 1):6370-83. doi: 10.1523/JNEUROSCI.14-11-06370.1994.

DOI:10.1523/JNEUROSCI.14-11-06370.1994
PMID:7965042
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6577226/
Abstract

Recently, the Dlx family of homeobox genes have been identified as candidates for regulating patterning and differentiation of the forebrain. We have made a polyclonal antiserum to the protein product of the Dlx-2 gene. Using this antiserum, we have characterized the spatial and temporal pattern of DLX-2 protein expression during murine development and in the adult mouse brain. These studies demonstrate that, like the mRNA from the Dlx-2 gene, DLX-2 protein is expressed in mouse embryonic forebrain, limbs, tail, genital tubercle, and branchial arches. Within the embryonic forebrain, DLX-2 protein is expressed within specific transverse and longitudinal domains. Analysis of expression within the wall of the forebrain shows that DLX-2 is expressed in proliferative regions including the ventricular and subventricular zones. DLX-2 is expressed in the same cells as MASH-1, a marker of relatively undifferentiated cells, but in a reciprocal fashion to MAP-2, a marker of terminal neuronal differentiation. A number of DLX-2-expressing cells, but not all, can be labeled with bromodeoxyuridine (BrdU). Using the patterns of DLX-2, MASH-1, MAP-2 expression, and bromodeoxyuridine incorporation, we identify four molecularly distinct populations of cells that may correspond to different stages of neuronal differentiation in the mouse basal forebrain, in which DLX-2 is expressed at the transition from proliferation to terminal differentiation.

摘要

最近,同源异型盒基因的Dlx家族已被确定为调节前脑模式形成和分化的候选基因。我们制备了针对Dlx-2基因蛋白质产物的多克隆抗血清。利用这种抗血清,我们已对小鼠发育过程中和成年小鼠脑中DLX-2蛋白表达的时空模式进行了表征。这些研究表明,与Dlx-2基因的mRNA一样,DLX-2蛋白在小鼠胚胎前脑、四肢、尾巴、生殖结节和鳃弓中表达。在胚胎前脑内,DLX-2蛋白在特定的横向和纵向区域表达。对前脑壁内表达的分析表明,DLX-2在包括脑室和室下区在内的增殖区域表达。DLX-2与相对未分化细胞的标志物MASH-1在相同细胞中表达,但与终末神经元分化的标志物MAP-2呈相反方式表达。许多表达DLX-2的细胞(但不是全部)可用溴脱氧尿苷(BrdU)标记。利用DLX-2、MASH-1、MAP-2的表达模式以及溴脱氧尿苷掺入情况,我们确定了四个分子上不同的细胞群体,它们可能对应于小鼠基底前脑神经元分化的不同阶段,其中DLX-2在从增殖到终末分化的转变过程中表达。

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