Child Study Center, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06520, USA.
Mol Cell Neurosci. 2010 Aug;44(4):362-73. doi: 10.1016/j.mcn.2010.05.001. Epub 2010 May 12.
It is well established that cerebellar granule cell precursors (GCPs) initially derive from progenitors in the rhombic lip of the embryonic cerebellar primordium. GCPs proliferate and migrate tangentially across the cerebellum to form the external granule cell layer (EGL) in late embryogenesis and early postnatal development. It is unclear whether GCPs are specified exclusively in the embryonic rhombic lip or whether their precursor persists in the neonate. Using transgenic mice expressing DsRed under the human glial fibrillary acidic protein (hGFAP) promoter, we found 2 populations of DsRed(+) cells in the EGL in the first postnatal week defined by bright and faint DsRed-fluorescent signal. Bright DsRed(+) cells have a protein expression profile and electrophysiological characteristics typical of astrocytes, but faint DsRed(+) cells in the EGL and internal granule cell layer (IGL) express markers and physiological properties of immature neurons. To determine if these astroglial cells gave rise to GCPs, we genetically tagged them with EGFP or betagal reporter genes at postnatal day (P)3-P5 using a hGFAP promoter driven inducible Cre recombinase. We found that GFAP promoter(+) cells in the EGL are proliferative and express glial and neural stem cell markers. In addition, immature granule cells (GCs) en route to the IGL at P12 as well as GCs in the mature cerebellum, 30days after recombination, express the reporter protein, suggesting that GFAP promoter(+) cells in the EGL generate a subset of granule cells. The identification of glial cells which function as neuronal progenitor cells profoundly impacts our understanding of cellular plasticity in the developing cerebellum.
众所周知,小脑颗粒细胞前体细胞(GCPs)最初来源于胚胎小脑原基的菱唇中的祖细胞。GCPs 增殖并沿切线迁移穿过小脑,在胚胎晚期和出生后早期形成外颗粒细胞层(EGL)。目前尚不清楚 GCPs 是否仅在胚胎菱唇中特异性指定,或者它们的前体是否在新生儿中持续存在。使用表达 DsRed 的转基因小鼠,该 DsRed 在人神经胶质纤维酸性蛋白(hGFAP)启动子的控制下表达,我们在出生后第一周的 EGL 中发现了 2 种 DsRed(+)细胞群,其特征是明亮和暗淡的 DsRed 荧光信号。明亮的 DsRed(+)细胞具有典型的星形胶质细胞的蛋白表达谱和电生理特征,但 EGL 和内颗粒细胞层(IGL)中的暗淡 DsRed(+)细胞表达未成熟神经元的标志物和生理特性。为了确定这些星形胶质细胞是否产生 GCPs,我们在出生后第 3-5 天(P)使用 hGFAP 启动子驱动的诱导型 Cre 重组酶对其进行基因标记,并用 EGFP 或 betagal 报告基因标记。我们发现 EGL 中的 GFAP 启动子(+)细胞具有增殖能力,并表达神经胶质和神经干细胞标志物。此外,在 P12 时处于向 IGL 迁移途中的未成熟颗粒细胞(GCs)以及在重组后 30 天的成熟小脑中的 GC 表达报告蛋白,表明 EGL 中的 GFAP 启动子(+)细胞产生了一部分颗粒细胞。鉴定作为神经元祖细胞起作用的神经胶质细胞,深刻地影响了我们对发育中小脑细胞可塑性的理解。