Shen Wei-Bin, Plachez Céline, Mongi Aika S, Richards Linda J
Department of Anatomy and Neurobiology and The Program in Neuroscience, The University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Gene Expr Patterns. 2006 Jun;6(5):471-81. doi: 10.1016/j.modgep.2005.11.004. Epub 2006 Feb 2.
Cortical midline glia are critical to the formation of the corpus callosum during development. The glial wedge is a population of midline glia that is located at the corticoseptal boundary and expresses repulsive/growth-inhibitory molecules that guide callosal axons as they cross the midline. The glial wedge are the first cells within the cortex to express GFAP and thus may express molecules specific for glial maturation. The corticoseptal boundary is a genetically defined boundary between the cingulate cortex (dorsal telencephalon) and the septum (ventral telencephalon). The correct dorso-ventral position of this boundary is vital to the formation of both the glial wedge and the corpus callosum. Our aim was to identify genes expressed specifically within the glial wedge that might be involved in either glial differentiation, formation of the corticoseptal boundary or development of the corpus callosum. To identify such genes we have performed a differential display PCR screen comparing RNA isolated from the glial wedge with RNA isolated from control tissues such as the neocortex and septum, of embryonic day 17 mouse brains. Using 200 different combinations of primers, we identified and cloned 67 distinct gene fragments. In situ hybridization analysis confirmed the differential expression of many of the genes, and showed that clones G24F3, G39F8 and transcription factor LZIP have specific expression patterns in the telencephalon of embryonic and postnatal brains. An RNase Protection Assay (RPA) revealed that the expression of G39F8, G24F3 and LZIP increase markedly in the telencephalon at E16 and continue to be expressed until at least P0, during the period when the corpus callosum is forming.
皮质中线胶质细胞在发育过程中对胼胝体的形成至关重要。胶质楔是位于皮质-隔区边界的一群中线胶质细胞,它们表达排斥性/生长抑制性分子,在胼胝体轴突穿过中线时引导这些轴突。胶质楔是皮质内最早表达胶质纤维酸性蛋白(GFAP)的细胞,因此可能表达胶质成熟特有的分子。皮质-隔区边界是扣带回皮质(背侧端脑)和隔区(腹侧端脑)之间的一个由基因定义的边界。这个边界正确的背-腹位置对于胶质楔和胼胝体的形成都至关重要。我们的目的是鉴定在胶质楔中特异性表达的基因,这些基因可能参与胶质分化、皮质-隔区边界的形成或胼胝体的发育。为了鉴定这些基因,我们进行了差异显示PCR筛选,将从胚胎第17天小鼠脑的胶质楔中分离的RNA与从对照组织如新皮质和隔区中分离的RNA进行比较。使用200种不同的引物组合,我们鉴定并克隆了67个不同的基因片段。原位杂交分析证实了许多基因的差异表达,并表明克隆G24F3、G39F8和转录因子LZIP在胚胎期和出生后脑的端脑中具有特定的表达模式。核糖核酸酶保护分析(RPA)显示,在胼胝体形成期间,G39F8、G24F3和LZIP在端脑中的表达在胚胎第16天显著增加,并至少持续表达至出生后第0天。