SKArred 2 死亡:海马体的神经炎症破坏。

Autophagy Pub Date : 2024-11-01 Epub Date: 2024-07-10 DOI:10.1080/15548627.2024.2373675
Thomas Bajaj, Tim Ebert, Larissa J Dillmann, Clara Sokn, Nils C Gassen, Jakob Hartmann
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引用次数: 0

摘要

细胞对内在和外在信号的多种反应都趋向于大自噬/自噬,这是一种保守的分解代谢过程,在溶酶体中降解细胞质成分和细胞器,尤其是在饥饿或应激状态下。除蛋白质降解外,自噬还与真核细胞内的非常规蛋白质分泌和多级极化分类密切相关。分泌型自噬(SA)已被认为是一种新的机制,在这种机制中,自噬体与质膜融合,并积极参与分泌一系列细胞膜蛋白质,包括组织重塑因子和 IL1 家族的炎症分子。自噬作用部分受糖皮质激素反应性、HSP90 协同伴侣蛋白 FKBP5 和 SNARE 蛋白(SEC22B、SNAP23、SNAP29、STX3 和 STX4)成员的控制。SA 失调与包括癌症、细胞死亡和变性在内的多种炎症性病症有关。然而,关于 SA 及其调控的关键分子机制,以及它在神经炎症和神经变性中的作用,仍然扑朔迷离。为了进一步描述 SA 的特性并确定其在神经炎症过程中的参与,我们研究了小鼠大脑、小胶质细胞以及来自对照组和阿尔茨海默病病例的人类死后脑组织中与 SA 相关的蛋白质相互作用网络。我们证明,SA 通过 SKA2 和 FKBP5 信号传导调节神经炎症介导的神经退行性变。
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SKArred 2 death: neuroinflammatory breakdown of the hippocampus.

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.

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