a Department of Anesthesiology , University of Rochester , Rochester , NY , USA.
b Institute for Cell Biology , University of Bonn , Bonn , Germany.
Autophagy. 2019 Jul;15(7):1199-1213. doi: 10.1080/15548627.2019.1580096. Epub 2019 Mar 1.
A major cellular catabolic pathway in neurons is macroautophagy/autophagy, through which misfolded or aggregation-prone proteins are sequestered into autophagosomes that fuse with lysosomes, and are degraded. MAPT (microtubule-associated protein tau) is one of the protein clients of autophagy. Given that accumulation of hyperphosphorylated MAPT contributes to the pathogenesis of Alzheimer disease and other tauopathies, decreasing endogenous MAPT levels has been shown to be beneficial to neuronal health in models of these diseases. A previous study demonstrated that the HSPA/HSP70 co-chaperone BAG3 (BCL2-associated athanogene 3) facilitates endogenous MAPT clearance through autophagy. These findings prompted us to further investigate the mechanisms underlying BAG3-mediated autophagy in the degradation of endogenous MAPT. Here we demonstrate for the first time that BAG3 plays an important role in autophagic flux in the neurites of mature neurons (20-24 days in vitro [DIV]) through interaction with the post-synaptic cytoskeleton protein SYNPO (synaptopodin). Loss of either BAG3 or SYNPO impeded the fusion of autophagosomes and lysosomes predominantly in the post-synaptic compartment. A block of autophagy leads to accumulation of the autophagic receptor protein SQSTM1/p62 (sequestosome 1) as well as MAPT phosphorylated at Ser262 (p-Ser262). Furthermore, p-Ser262 appears to accumulate in autophagosomes at post-synaptic densities. Overall these data provide evidence of a novel role for the co-chaperone BAG3 in synapses. In cooperation with SYNPO, it functions as part of a surveillance complex that facilitates the autophagic clearance of MAPT p-Ser262, and possibly other MAPT species at the post-synapse. This appears to be crucial for the maintenance of a healthy, functional synapse.: aa: amino acids; ACTB: actin beta; BafA1: bafilomycin A BAG3: BCL2 associated athanogene 3; CQ chloroquine; CTSL: cathepsin L; DIV: days in vitro; DLG4/PSD95: discs large MAGUK scaffold protein 4; HSPA/HSP70: heat shock protein family A (Hsp70); MAP1LC3B/LC3B: microtubule associated protein 1 light chain 3 beta; MAP2: microtubule associated protein 2; MAPT: microtubule associated protein tau; p-Ser262: MAPT phosphorylated at serine 262; p-Ser396/404: MAPT phosphorylated at serines 396 and 404; p-Thr231: MAPT phosphorylated at threonine 231; PBS: phosphate buffered saline; PK: proteinase K; scr: scrambled; shRNA: short hairpin RNA; SQSTM1/p62 sequestosome 1; SYN1: synapsin I; SYNPO synaptopodin; SYNPO2/myopodin: synaptopodin 2; VPS: vacuolar protein sorting.
神经元中主要的细胞分解代谢途径是巨自噬/自噬,通过该途径,错误折叠或易于聚集的蛋白质被隔离到自噬体中,自噬体与溶酶体融合,并被降解。MAPT(微管相关蛋白 tau)是自噬的蛋白质客户之一。鉴于过度磷酸化的 MAPT 的积累有助于阿尔茨海默病和其他 tau 病的发病机制,降低内源性 MAPT 水平已被证明对这些疾病模型中的神经元健康有益。先前的研究表明,HSPA/HSP70 共伴侣 BAG3(BCL2 相关的 Athanogene 3)通过自噬促进内源性 MAPT 的清除。这些发现促使我们进一步研究 BAG3 介导的自噬在降解内源性 MAPT 中的机制。在这里,我们首次证明 BAG3 通过与突触后细胞骨架蛋白 SYNPO(突触小体蛋白)相互作用,在成熟神经元(体外 20-24 天)的神经突中发挥重要作用,促进自噬通量。BAG3 或 SYNPO 的缺失均主要阻碍了自噬体与溶酶体的融合。自噬的阻断会导致自噬受体蛋白 SQSTM1/p62(自噬体 1)以及在丝氨酸 262 处磷酸化的 MAPT(p-Ser262)的积累。此外,p-Ser262 似乎在突触后密度处积累在自噬体中。总的来说,这些数据为共伴侣 BAG3 在突触中的新作用提供了证据。它与 SYNPO 合作,作为监视复合物的一部分发挥作用,该复合物促进 MAPT p-Ser262 的自噬清除,以及可能在突触后发生的其他 MAPT 物种。这对于维持健康、功能正常的突触至关重要。