McLear Julie A, Garcia-Fresco German, Bhat Manzoor A, Van Dyke Terry A
Curriculum in Neurobiology, UNC Neuroscience Center and Neurodevelopmental Disorders Research Center, Chapel Hill, NC 27599-7295, USA.
Mol Cell Neurosci. 2006 Nov;33(3):260-73. doi: 10.1016/j.mcn.2006.07.012. Epub 2006 Sep 18.
Nestin-positive cells were targeted for pRb, p107 and p130 (pRb(f)) inactivation by expression of T(121), a truncated SV40 large T antigen that selectively binds to and inactivates pRb(f). Cre expression was initiated under GFAP control, resulting in T(121) expression restricted to neuroprogenitor cells beginning at embryonic day 11.5 (E11.5). Bi-transgenic embryos showed aberrant central nervous system (CNS) cell proliferation and apoptosis by E13.5. Defects in cortical development were evident with primary effects resulting in depletion of neural progenitors and aberrant cellular migration. Consequently, juvenile and adult brain morphology was reproducibly abnormal, including disorganization of neocortical, hippocampal and cerebellar regions. These aberrations resulted in behavioral phenotypes, including ataxia and seizures. The data indicate that inactivation of pRb(f) in radial glial cells, a population of neuroprogenitor cells, leads to specific disruptions in CNS patterning. The neuroprogenitor-restricted transgene expression provides a model in which to explore both developmental mechanisms and functional neurological outcomes.
通过表达T(121)(一种截短的SV40大T抗原,可选择性结合并使pRb(f)失活),将巢蛋白阳性细胞作为pRb、p107和p130(pRb(f))失活的靶点。Cre表达在GFAP控制下启动,导致T(121)的表达从胚胎第11.5天(E11.5)开始局限于神经祖细胞。双转基因胚胎在E13.5时显示出中枢神经系统(CNS)细胞增殖异常和凋亡。皮质发育缺陷明显,主要影响是神经祖细胞耗竭和细胞迁移异常。因此,幼年和成年大脑形态反复出现异常,包括新皮质、海马体和小脑区域的紊乱。这些畸变导致行为表型,包括共济失调和癫痫发作。数据表明,放射状胶质细胞(一种神经祖细胞群体)中pRb(f)的失活会导致CNS模式的特定破坏。神经祖细胞限制的转基因表达提供了一个模型,可用于探索发育机制和功能性神经学结果。