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SKArred 2 死亡:海马体的神经炎症崩溃。

SKArred 2 death: neuroinflammatory breakdown of the hippocampus.

机构信息

Research Group Neurohomeostasis, Department of Psychiatry and Psychotherapy, University of Bonn, Bonn, Germany.

Department of Psychiatry, Harvard Medical School, McLean Hospital, Belmont, MA, USA.

出版信息

Autophagy. 2024 Nov;20(11):2581-2583. doi: 10.1080/15548627.2024.2373675. Epub 2024 Jul 10.

Abstract

A multitude of cellular responses to intrinsic and extrinsic signals converge on macroautophagy/autophagy, a conserved catabolic process that degrades cytoplasmic constituents and organelles in the lysosome, particularly during starvation or stress. In addition to protein degradation, autophagy is deeply interconnected with unconventional protein secretion and polarized sorting at multiple levels within eukaryotic cells. Secretory autophagy (SA) has been recognized as a novel mechanism in which autophagosomes fuse with the plasma membrane and actively participate in the secretion of a series of cytosolic proteins, ranging from tissue remodeling factors to inflammatory molecules of the IL1 family. SA is partially controlled by the glucocorticoid-responsive, HSP90 co-chaperone FKBP5 and members of the SNARE proteins, SEC22B, SNAP23, SNAP29, STX3 and STX4. SA deregulation is implicated in several inflammatory pathologies, including cancer, cell death and degeneration. However, the key molecular mechanisms governing SA and its regulation remain elusive, as does its role in neuroinflammation and neurodegeneration. To further characterize SA and pinpoint its involvement in neuroinflammatory processes, we studied SA-relevant protein interaction networks in mouse brain, microglia and human postmortem brain tissue from control subjects and Alzheimer disease cases. We demonstrate that SA regulates neuroinflammation-mediated neurodegeneration via SKA2 and FKBP5 signaling.

摘要

大量细胞对内源性和外源性信号的反应都集中在巨自噬/自噬上,这是一种保守的分解代谢过程,可在溶酶体中降解细胞质成分和细胞器,特别是在饥饿或应激期间。除了蛋白质降解,自噬与非传统的蛋白质分泌和真核细胞内多个水平的极化分选密切相关。分泌自噬(SA)已被认为是一种新的机制,其中自噬体与质膜融合,并积极参与一系列细胞质蛋白的分泌,范围从组织重塑因子到白细胞介素 1 家族的炎症分子。SA 部分受糖皮质激素反应性 HSP90 共伴侣 FKBP5 和 SNARE 蛋白 SEC22B、SNAP23、SNAP29、STX3 和 STX4 的控制。SA 失调与几种炎症性病理有关,包括癌症、细胞死亡和变性。然而,控制 SA 的关键分子机制及其调节仍然难以捉摸,其在神经炎症和神经退行性变中的作用也是如此。为了进一步表征 SA 并确定其在神经炎症过程中的作用,我们研究了来自对照受试者和阿尔茨海默病病例的小鼠大脑、小胶质细胞和人死后脑组织中的与 SA 相关的蛋白质相互作用网络。我们证明,SA 通过 SKA2 和 FKBP5 信号调节神经炎症介导的神经退行性变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb80/11572194/1e9d740c8bfd/KAUP_A_2373675_F0001_C.jpg

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