Division of Experimental Hematology and Cancer Biology, Department of Pediatrics, Cincinnati Children's Hospital University of Cincinnati, Cincinnati, Ohio.
Glia. 2013 Nov;61(11):1906-21. doi: 10.1002/glia.22567. Epub 2013 Sep 6.
The Rho family GTPase Cdc42 has been implicated in developmental Schwann cell (SC) proliferation, providing sufficient SCs for radial sorting of axons preceding SC differentiation in the peripheral nervous system. We generated Cdc42 conditional knockout (Cdc42-CKO) mice and confirmed aberrant axon sorting in Cdc42-CKO nerves. In adult Cdc42-CKO nerves, blood vessels were enlarged, and mature Remak bundles containing small axons were absent. Abnormal infoldings and outfoldings of myelin sheaths developed in Cdc42-CKO nerves, mimicking pathological features of Charcot-Marie-Tooth (CMT) disease. The NF2/merlin tumor suppressor has been implicated up- and down-stream of Cdc42. In Cdc42-CKO;NF2-del double mutant mice, radial sorting defects seen in Cdc42-CKO nerves were rescued, while changes in myelin sheaths in Cdc42-CKO nerves were not. Phosphorylation of Focal adhesion kinase (FAK) and P-GSK3β, as well as expression of β-catenin were decreased in Cdc42-CKO nerves, and these changes were rescued by NF2/merlin mutation in Cdc42-CKO;NF2-del double mutant mice. Thus, Cdc42 regulates SC radial sorting in vivo through NF2/merlin dependent signaling pathways, while Cdc42 modulation of myelin sheath folding is NF2/merlin independent.
Rho 家族 GTP 酶 Cdc42 已被牵连到发育中的施万细胞 (SC) 增殖中,为外周神经系统中 SC 分化前的轴突放射状分选提供了足够的 SC。我们生成了 Cdc42 条件性敲除 (Cdc42-CKO) 小鼠,并证实了 Cdc42-CKO 神经中的异常轴突分选。在成年 Cdc42-CKO 神经中,血管增大,并且缺乏包含小轴突的成熟 Remak 束。Cdc42-CKO 神经中出现了异常的髓鞘内褶和外褶,模拟了 Charcot-Marie-Tooth (CMT) 疾病的病理特征。NF2/merlin 肿瘤抑制因子已被牵连到 Cdc42 的上下游。在 Cdc42-CKO;NF2-del 双突变小鼠中,Cdc42-CKO 神经中观察到的放射状分选缺陷得到了挽救,而 Cdc42-CKO 神经中髓鞘的变化没有得到挽救。Cdc42-CKO 神经中的黏着斑激酶 (FAK) 和 P-GSK3β 的磷酸化以及β-连环蛋白的表达减少,而这些变化在 Cdc42-CKO;NF2-del 双突变小鼠中通过 NF2/merlin 突变得到了挽救。因此,Cdc42 通过 NF2/merlin 依赖的信号通路调节体内 SC 的放射状分选,而 Cdc42 对髓鞘折叠的调节是 NF2/merlin 独立的。