细胞质
伴侣(临床)
化学
相变
热休克蛋白
生物物理学
细胞生物学
生物化学
生物
热力学
医学
基因
物理
病理
作者
Shan Lu,Jiaojiao Hu,Olubankole Aladesuyi Arogundade,Alexander Goginashvili,Sonia Vazquez‐Sanchez,Jolene K. Diedrich,Jinge Gu,Jacob A. Blum,Spencer Oung,Qiaozhen Ye,Haiyang Yu,John Ravits,Cong Liu,John R. Yates,Don W. Cleveland
标识
DOI:10.1038/s41556-022-00988-8
摘要
While acetylated, RNA-binding-deficient TDP-43 reversibly phase separates within nuclei into complex droplets (anisosomes) comprised of TDP-43-containing liquid outer shells and liquid centres of HSP70-family chaperones, cytoplasmic aggregates of TDP-43 are hallmarks of multiple neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS). Here we show that transient oxidative stress, proteasome inhibition or inhibition of the ATP-dependent chaperone activity of HSP70 provokes reversible cytoplasmic TDP-43 de-mixing and transition from liquid to gel/solid, independently of RNA binding or stress granules. Isotope labelling mass spectrometry was used to identify that phase-separated cytoplasmic TDP-43 is bound by the small heat-shock protein HSPB1. Binding is direct, mediated through TDP-43's RNA binding and low-complexity domains. HSPB1 partitions into TDP-43 droplets, inhibits TDP-43 assembly into fibrils, and is essential for disassembly of stress-induced TDP-43 droplets. A decrease in HSPB1 promotes cytoplasmic TDP-43 de-mixing and mislocalization. HSPB1 depletion was identified in spinal motor neurons of patients with ALS containing aggregated TDP-43. These findings identify HSPB1 to be a regulator of cytoplasmic TDP-43 phase separation and aggregation.
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