Nuber Silke, Hsiang Harrison, Keewan Esra'a, Moors Tim E, Reitz Sydney J, Tiwari Anupama, Ho Gary Ph, Su Elena, Hahn Wolf, Adom Marie-Alexandre, Pathak Riddhima, Blizzard Matthew, Kim Sangjune, Ko Han Seok, Zhang Xiaoqun, Svenningsson Per, Selkoe Dennis J, Fanning Saranna
Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Department of Neurology and.
JCI Insight. 2025 Jun 3;10(13). doi: 10.1172/jci.insight.188413. eCollection 2025 Jul 8.
Loss-of-function mutations in the GBA1 gene are a prevalent risk factor for Parkinson's disease (PD). Defining features are Lewy bodies that can be rich in α-synuclein (αS), vesicle membranes, and other lipid membranes, coupled with striatal dopamine loss and progressive motor dysfunction. Of these, lipid abnormalities are the least understood. An altered lipid metabolism in PD patient-derived neurons - carrying mutations in either GBA1, encoding for glucocerebrosidase (GCase), or αS - shifted the physiological αS tetramer/monomer (T:M) equilibrium, resulting in PD phenotypes. We previously reported inhibition of stearoyl-CoA desaturase (SCD), the rate-limiting enzyme for fatty acid desaturation, stabilized αS tetramers and improved motor deficits in αS mice. Here we show that mutant GBA1-PD cultured neurons have increased SCD products (monounsaturated fatty acids [MUFAS]) and reduced αS T:M ratios that were improved by inhibiting SCD. Oral treatment of symptomatic L444P and E326K Gba1 mutant mice with 5b also improved the αS T:M homeostasis and dopaminergic striatal integrity. Moreover, SCD inhibition normalized GCase maturation and dampened lysosomal and lipid-rich clustering, key features of neuropathology in GBA-PD. In conclusion, this study supports that brain MUFA metabolism links GBA1 genotype and WT αS homeostasis to downstream neuronal and behavioral impairments, identifying SCD as a therapeutic target for GBA-PD.
GBA1基因功能丧失突变是帕金森病(PD)的常见风险因素。其典型特征是路易小体,其中富含α-突触核蛋白(αS)、囊泡膜和其他脂质膜,同时伴有纹状体多巴胺丧失和进行性运动功能障碍。其中,脂质异常最不为人所了解。在源自PD患者的神经元中,编码葡萄糖脑苷脂酶(GCase)的GBA1或αS发生突变,导致脂质代谢改变,从而改变了生理性αS四聚体/单体(T:M)平衡,进而导致PD表型。我们之前报道,抑制脂肪酸去饱和的限速酶硬脂酰辅酶A去饱和酶(SCD)可稳定αS四聚体,并改善αS小鼠的运动缺陷。在此,我们表明,突变型GBA1-PD培养神经元的SCD产物(单不饱和脂肪酸 [MUFAS])增加,αS T:M比率降低,而抑制SCD可改善这一情况。用5b对有症状的L444P和E326K Gba1突变小鼠进行口服治疗,也改善了αS T:M稳态和多巴胺能纹状体完整性。此外,抑制SCD可使GCase成熟正常化,并减轻溶酶体和富含脂质的聚集,这些是GBA-PD神经病理学的关键特征。总之,本研究支持大脑单不饱和脂肪酸代谢将GBA1基因型和野生型αS稳态与下游神经元和行为损伤联系起来,确定SCD为GBA-PD的治疗靶点。