Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Institute of Parkinson and Movement Disorder, Zhengzhou University, Zhengzhou, China.
Acta Neuropathol. 2023 May;145(5):681-705. doi: 10.1007/s00401-023-02560-6. Epub 2023 Mar 16.
Cerebral small vessel disease (CSVD) is a prominent cause of ischemic and hemorrhagic stroke and a leading cause of vascular dementia, affecting small penetrating vessels of the brain. Despite current advances in genetic susceptibility studies, challenges remain in defining the causative genes and the underlying pathophysiological mechanisms. Here, we reported that the ARHGEF15 gene was a causal gene linked to autosomal dominant inherited CSVD. We identified one heterozygous nonsynonymous mutation of the ARHGEF15 gene that cosegregated completely in two families with CSVD, and a heterozygous nonsynonymous mutation and a stop-gain mutation in two individuals with sporadic CSVD, respectively. Intriguingly, clinical imaging and pathological findings displayed severe osteoporosis and even osteoporotic fractures in all the ARHGEF15 mutation carriers. In vitro experiments indicated that ARHGEF15 mutations resulted in RhoA/ROCK2 inactivation-induced F-actin cytoskeleton disorganization in vascular smooth muscle cells and endothelial cells and osteoblast dysfunction by inhibiting the Wnt/β-catenin signaling pathway in osteoblast cells. Furthermore, Arhgef15-e(V368M)1 transgenic mice developed CSVD-like pathological and behavioral phenotypes, accompanied by severe osteoporosis. Taken together, our findings provide strong evidence that loss-of-function mutations of the ARHGEF15 gene cause CSVD accompanied by osteoporotic fracture.
脑小血管病 (CSVD) 是缺血性和出血性中风的主要原因,也是血管性痴呆的主要原因,影响大脑的小穿透血管。尽管目前在遗传易感性研究方面取得了进展,但在确定致病基因和潜在病理生理机制方面仍存在挑战。在这里,我们报道了 ARHGEF15 基因是与常染色体显性遗传 CSVD 相关的因果基因。我们在两个 CSVD 家族中发现了 ARHGEF15 基因的一个杂合非同义突变,该突变完全共分离,在两个散发性 CSVD 个体中分别发现了一个杂合非同义突变和一个无义突变。有趣的是,所有 ARHGEF15 突变携带者的临床影像学和病理学表现均显示严重的骨质疏松症,甚至骨质疏松性骨折。体外实验表明,ARHGEF15 突变导致 RhoA/ROCK2 失活,引起血管平滑肌细胞和内皮细胞中 F-肌动蛋白细胞骨架紊乱,并通过抑制成骨细胞中的 Wnt/β-连环蛋白信号通路导致成骨细胞功能障碍。此外,Arhgef15-e(V368M)1 转基因小鼠表现出 CSVD 样的病理和行为表型,伴有严重的骨质疏松症。总之,我们的研究结果提供了有力的证据,证明 ARHGEF15 基因的功能丧失突变导致 CSVD 伴发骨质疏松性骨折。