Department of Psychiatry and Biobehavioral Sciences, Intellectual and Developmental Disabilities Research Center, University of California, Los Angeles, CA 90095; and.
Department of Psychiatry and Biobehavioral Sciences, Intellectual and Developmental Disabilities Research Center, University of California, Los Angeles, CA 90095; and
Proc Natl Acad Sci U S A. 2014 May 20;111(20):7444-9. doi: 10.1073/pnas.1400422111. Epub 2014 May 5.
The studies on the exact lineage composition of NG2 expressing progenitors in the forebrain have been controversial. A number of studies have revealed the heterogeneous nature of postnatal NG2 cells. However, NG2 cells found in embryonic dates are far less understood. Our study indicates that early NG2 progenitors from a ventral origin (i.e., before embryonic day 16.5) tangentially migrate out of the medial ganglionic eminence and give rise to interneurons in deep layers of the dorsal cerebral cortex. The majority of myelinating oligodendrocytes found in both cortical gray and white matters are, in contrast, derived from NG2 progenitors with a neonatal subventricular zone origin. Our lineage tracing data reflect the heterogeneous nature of NG2 progenitor populations and define the relationship between lineage divergence and spatiotemporal origins. Beyond the typical lineage tracing studies of NG2(+) cells, by costaining with lineage-specific markers, our study addresses the origins of heterogeneity and its implications in the differentiation potentials of NG2(+) progenitors.
关于前脑 NG2 表达祖细胞的确切谱系组成的研究一直存在争议。许多研究揭示了产后 NG2 细胞的异质性。然而,对胚胎期的 NG2 细胞了解甚少。我们的研究表明,来自腹侧起源的早期 NG2 祖细胞(即在胚胎第 16.5 天之前)沿切线方向从内侧神经节隆起向外迁移,并在大脑背侧皮层的深层产生中间神经元。相比之下,在皮质灰质和白质中发现的大多数髓鞘少突胶质细胞是源自具有新生儿侧脑室下区起源的 NG2 祖细胞。我们的谱系追踪数据反映了 NG2 祖细胞群体的异质性,并定义了谱系分化和时空起源之间的关系。除了对 NG2(+)细胞的典型谱系追踪研究之外,通过与谱系特异性标志物共染色,我们的研究解决了 NG2(+)祖细胞异质性的起源及其对分化潜能的影响。