Doan Ryan A, Monk Kelly R
The Vollum Institute, Oregon Health & Science University , Portland, OR, USA.
J Cell Biol. 2025 May 5;224(5). doi: 10.1083/jcb.202311041. Epub 2025 Mar 19.
Schwann cells, the myelinating glia of the peripheral nervous system (PNS), are critical for myelin development, maintenance, and repair. Rac1 is a known regulator of radial sorting, a key step in developmental myelination. Previously, in zebrafish, we showed that the loss of Dock1, a Rac1-specific guanine nucleotide exchange factor, resulted in delayed peripheral myelination during development. Here, we demonstrate that Dock1 is necessary for myelin maintenance and remyelination after injury in adult zebrafish. Furthermore, Dock1 performs an evolutionarily conserved role in mice, functioning cell autonomously in Schwann cells to regulate the development, maintenance, and repair of peripheral myelin. Pharmacological and genetic manipulation of Rac1 in larval zebrafish, along with the analysis of active Rac1 levels in developing Dock1 mutant mouse nerves, revealed an interaction between these two proteins. We propose that the interplay between Dock1 and Rac1 signaling in Schwann cells is required to establish, maintain, and facilitate repair and remyelination within the PNS.
施万细胞是周围神经系统(PNS)的髓鞘形成神经胶质细胞,对髓鞘的发育、维持和修复至关重要。Rac1是已知的径向分选调节因子,是发育性髓鞘形成的关键步骤。此前,我们在斑马鱼中发现,Rac1特异性鸟嘌呤核苷酸交换因子Dock1的缺失导致发育过程中周围髓鞘形成延迟。在此,我们证明Dock1对成年斑马鱼损伤后的髓鞘维持和髓鞘再生是必需的。此外,Dock1在小鼠中发挥进化上保守的作用,在施万细胞中自主发挥功能,以调节周围髓鞘的发育、维持和修复。对斑马鱼幼体中Rac1进行药理学和遗传学操作,以及对发育中的Dock1突变小鼠神经中活性Rac1水平的分析,揭示了这两种蛋白之间的相互作用。我们提出,施万细胞中Dock1和Rac1信号之间的相互作用对于在PNS内建立、维持和促进修复及髓鞘再生是必需的。