分子伴侣对生理和病理凝聚的调控。

Nadeen Akaree, Valentina Secco, Flonia Levy-Adam, Amal Younis, Serena Carra, Reut Shalgi
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摘要

生物分子凝聚体是动态的无膜室,调节着无数的细胞功能。一种特殊类型的生理凝聚物称为应激颗粒(SGs),由于其在细胞应激反应和各种疾病中的作用而越来越受到关注。SGs由数百种rna结合蛋白组成,在应激反应中短暂形成,以保护mrna在应激消退时不被翻译和分解。有趣的是,SGs含有几种易于聚集的蛋白,如TDP-43、FUS、hnRNPA1等,这些蛋白通常存在于肌萎缩侧索硬化症(ALS)和额颞叶痴呆(FTD)患者尸检组织的病理包涵体中。此外,这些基因的突变会导致家族性ALS和FTD。这导致研究人员提出,病态聚集是由异常的SGs播下的种子:SGs不能正确地分解,失去其动态特性,成为病理凝聚体,最终“成熟”成聚集体。在这里,我们讨论了各种ALS/ ftd相关蛋白支持该模型的证据。我们将进一步关注分子伴侣介导的ALS/ ftd相关生理凝聚和病理凝聚的调控。除SGs外,我们还综述了与ALS/ ftd相关的核凝析物,即副斑体、各向异性和核核淀粉样体,并讨论了它们在伴侣蛋白的调控作用。由于大多数伴侣机制调节生理凝聚物的分解,我们强调了不同伴侣家族的生理和病理凝聚调节的平行主题,强调了早期疾病干预的潜力。
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Regulation of physiological and pathological condensates by molecular chaperones.

Biomolecular condensates are dynamic membraneless compartments that regulate a myriad of cellular functions. A particular type of physiological condensate called stress granules (SGs) has gained increasing interest due to its role in the cellular stress response and various diseases. SGs, composed of several hundred RNA-binding proteins, form transiently in response to stress to protect mRNAs from translation and disassemble when the stress subsides. Interestingly, SGs contain several aggregation-prone proteins, such as TDP-43, FUS, hnRNPA1, and others, which are typically found in pathological inclusions seen in autopsy tissues from amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) patients. Moreover, mutations in these genes lead to the familial form of ALS and FTD. This has led researchers to propose that pathological aggregation is seeded by aberrant SGs: SGs that fail to properly disassemble, lose their dynamic properties, and become pathological condensates which finally 'mature' into aggregates. Here, we discuss the evidence supporting this model for various ALS/FTD-associated proteins. We further continue to focus on molecular chaperone-mediated regulation of ALS/FTD-associated physiological condensates on one hand, and pathological condensates on the other. In addition to SGs, we review ALS/FTD-relevant nuclear condensates, namely paraspeckles, anisosomes, and nucleolar amyloid bodies, and discuss their emerging regulation by chaperones. As the majority of chaperoning mechanisms regulate physiological condensate disassembly, we highlight parallel themes of physiological and pathological condensation regulation across different chaperone families, underscoring the potential for early disease intervention.

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