Department of Cell Biology, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA.
Department of Biochemistry, Hunter James Kelly Research Institute, Jacobs School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, NY 14203, USA.
Brain. 2022 Mar 29;145(1):168-178. doi: 10.1093/brain/awab249.
Agents that raise cyclic guanosine monophosphate (cGMP) by activating protein kinase G increase 26S proteasome activities, protein ubiquitination and degradation of misfolded proteins. Therefore, they may be useful in treating neurodegenerative and other diseases caused by an accumulation of misfolded proteins. Mutations in myelin protein zero (MPZ) cause the peripheral neuropathy Charcot-Marie-Tooth type 1B (CMT1B). In peripheral nerves of a mouse model of CMT1B, where the mutant MPZS63del is expressed, proteasome activities are reduced, mutant MPZS63del and polyubiquitinated proteins accumulate and the unfolded protein response (p-eif2α) is induced. In HEK293 cells, raising cGMP stimulated ubiquitination and degradation of MPZS63del, but not of wild-type MPZ. Treating S63del mice with the phosphodiesterase 5 inhibitor, sildenafil-to raise cGMP-increased proteasome activity in sciatic nerves and reduced the levels of polyubiquitinated proteins, the proteasome reporter ubG76V-GFP and p-elF2α. Furthermore, sildenafil treatment reduced the number of amyelinated axons, and increased myelin thickness and nerve conduction velocity in sciatic nerves. Thus, agents that raise cGMP, including those widely used in medicine, may be useful therapies for CMT1B and other proteotoxic diseases.
通过激活蛋白激酶 G 来提高环鸟苷酸单磷酸 (cGMP) 的药物可增加 26S 蛋白酶体的活性、蛋白质泛素化以及错误折叠蛋白质的降解。因此,它们可能对治疗由错误折叠蛋白质积累引起的神经退行性疾病和其他疾病有用。髓鞘蛋白零 (MPZ) 的突变会导致周围神经病变夏科-马里-图思病 1B 型(CMT1B)。在 CMT1B 的小鼠模型的周围神经中,表达突变型 MPZS63del,蛋白酶体的活性降低,突变型 MPZS63del 和多泛素化蛋白质积累,未折叠蛋白反应 (p-eif2α) 被诱导。在 HEK293 细胞中,提高 cGMP 可刺激 MPZS63del 的泛素化和降解,但对野生型 MPZ 则没有效果。用磷酸二酯酶 5 抑制剂西地那非(sildenafil)治疗 S63del 小鼠——提高 cGMP 以增加坐骨神经中的蛋白酶体活性,并降低多泛素化蛋白质、蛋白酶体报告 ubG76V-GFP 和 p-elF2α 的水平。此外,西地那非治疗还减少了无髓鞘轴突的数量,并增加了坐骨神经中的髓鞘厚度和神经传导速度。因此,提高 cGMP 的药物,包括在医学中广泛使用的药物,可能对 CMT1B 和其他蛋白毒性疾病是有用的治疗方法。