Department of Neurology, Louisiana State University Health Sciences Center, 1501 Kings Highway, Shreveport, LA 71130, USA.
Department of Cellular Biology and Anatomy, Louisiana State University Health Sciences Center, 1501 Kings Highway, Shreveport, LA 71130, USA.
Neurobiol Dis. 2015 Jan;73:189-203. doi: 10.1016/j.nbd.2014.09.006. Epub 2014 Sep 22.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a Notch3 dominant mutation-induced cerebral small vascular disease, is characterized by progressive degeneration of vascular smooth muscle cells (vSMCs) of small arteries in the brain, leading to recurrent ischemic stroke, vascular dementia and death. To date, no treatment can stop or delay the progression of this disease. Herein, we determined the therapeutic effects of stem cell factor (SCF) in combination with granulocyte colony-stimulating factor (G-CSF) (SCF+G-CSF) in a mouse model of CADASIL carrying the human mutant Notch3 gene. SCF+G-CSF was subcutaneously administered for 5 days and repeated 4 times with 1-4 month intervals. We found through water maze testing that SCF+G-CSF treatment improved cognitive function. SCF+G-CSF also attenuated vSMC degeneration in small arteries, increased cerebral blood vascular density, and inhibited apoptosis in CADASIL mice. We also discovered that loss of cerebral capillary endothelial cells and neural stem cells/neural progenitor cells (NSCs/NPCs) occurred in CADASIL mice. SCF+G-CSF treatment inhibited the CADASIL-induced cell loss in the endothelia and NSCs/NPCs and promoted neurogenesis. In an in vitro model of apoptosis, SCF+G-CSF prevented apoptotic cell death in vSMCs through AKT signaling and by inhibiting caspase-3 activity. These data suggest that SCF+G-CSF restricts the pathological progression of CADASIL. This study offers new insights into developing therapeutic strategies for CADASIL.
伴有皮质下梗死和白质脑病的脑常染色体显性动脉病(CADASIL)是一种 Notch3 显性突变诱导的脑小血管疾病,其特征是脑小动脉的血管平滑肌细胞(vSMCs)进行性退化,导致复发性缺血性中风、血管性痴呆和死亡。迄今为止,尚无治疗方法可以阻止或延缓该病的进展。在此,我们在携带人类突变 Notch3 基因的 CADASIL 小鼠模型中确定了干细胞因子(SCF)与粒细胞集落刺激因子(G-CSF)(SCF+G-CSF)联合治疗的疗效。SCF+G-CSF 经皮下给药 5 天,间隔 1-4 个月重复 4 次。通过水迷宫测试,我们发现 SCF+G-CSF 治疗可改善认知功能。SCF+G-CSF 还可减轻 CADASIL 小鼠小动脉中 vSMC 的退化,增加脑血血管密度,并抑制细胞凋亡。我们还发现 CADASIL 小鼠中发生了脑毛细血管内皮细胞和神经干细胞/神经前体细胞(NSCs/NPCs)的丢失。SCF+G-CSF 治疗可抑制 CADASIL 诱导的内皮细胞和 NSCs/NPCs 细胞丢失,并促进神经发生。在体外细胞凋亡模型中,SCF+G-CSF 通过 AKT 信号通路和抑制 caspase-3 活性来防止 vSMCs 的凋亡性细胞死亡。这些数据表明,SCF+G-CSF 限制了 CADASIL 的病理进展。本研究为 CADASIL 的治疗策略提供了新的见解。