Chen Chunling, Merrill Ronald A, Jong Chian Ju, Strack Stefan
Department of Neuroscience and Pharmacology, University of Iowa, Carver College of Medicine, Bowen Science Building, 51 Newton Road, Iowa City, IA, 52242, USA.
Department of Molecular Physiology and Biophysics, University of Iowa, Carver College of Medicine, Bowen Science Building, 51 Newton Road, Iowa City, IA, 52242, USA.
Cerebellum. 2024 Oct;23(5):2042-2049. doi: 10.1007/s12311-024-01701-1. Epub 2024 May 13.
Autosomal-recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is caused by loss-of-function mutation in the SACS gene, which encodes sacsin, a putative HSP70-HSP90 co-chaperone. Previous studies with Sacs knock-out (KO) mice and patient-derived fibroblasts suggested that SACSIN mutations inhibit the function of the mitochondrial fission enzyme dynamin-related protein 1 (Drp1). This in turn resulted in mitochondrial hyperfusion and dysfunction. We experimentally tested this hypothesis by genetically manipulating the mitochondrial fission/fusion equilibrium, creating double KO (DKO) mice that also lack positive (PP2A/Bβ2) and negative (PKA/AKAP1) regulators of Drp1. Neither promoting mitochondrial fusion (Bβ2 KO) nor fission (Akap1 KO) influenced progression of motor symptoms in Sacs KO mice. However, our studies identified profound learning and memory deficits in aged Sacs KO mice. Moreover, this cognitive impairment was rescued in a gene dose-dependent manner by deletion of the Drp1 inhibitor PKA/Akap1. Our results are inconsistent with mitochondrial dysfunction as a primary pathogenic mechanism in ARSACS. Instead, they imply that promoting mitochondrial fission may be beneficial at later stages of the disease when pathology extends to brain regions subserving learning and memory.
夏尔沃瓦-萨格奈常染色体隐性痉挛性共济失调(ARSACS)由SACS基因突变导致功能丧失引起,该基因编码sacsin,一种假定的HSP70-HSP90共伴侣蛋白。先前对Sacs基因敲除(KO)小鼠和患者来源的成纤维细胞的研究表明,SACSIN突变会抑制线粒体分裂酶动力相关蛋白1(Drp1)的功能。这进而导致线粒体过度融合和功能障碍。我们通过基因操作线粒体分裂/融合平衡对这一假设进行了实验验证,创建了同时缺乏Drp1正向(PP2A/Bβ2)和负向(PKA/AKAP1)调节因子的双基因敲除(DKO)小鼠。促进线粒体融合(Bβ2基因敲除)或分裂(Akap1基因敲除)均未影响Sacs基因敲除小鼠运动症状的进展。然而,我们的研究发现老年Sacs基因敲除小鼠存在严重的学习和记忆缺陷。此外,通过缺失Drp1抑制剂PKA/Akap1,这种认知障碍以基因剂量依赖的方式得到了挽救。我们的结果与线粒体功能障碍作为ARSACS主要致病机制的观点不一致。相反,这意味着在疾病后期病理扩展到负责学习和记忆的脑区时,促进线粒体分裂可能有益。