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无机多聚磷酸盐、线粒体与神经退行性变。

Inorganic Polyphosphate, Mitochondria, and Neurodegeneration.

机构信息

Department of Biology, Rutgers University, Camden, NJ, USA.

出版信息

Prog Mol Subcell Biol. 2022;61:27-49. doi: 10.1007/978-3-031-01237-2_3.

Abstract

With an aging population, the presence of aging-associated pathologies is expected to increase within the next decades. Regrettably, we still do not have any valid pharmacological or non-pharmacological tools to prevent, revert, or cure these pathologies. The absence of therapeutical approaches against aging-associated pathologies can be at least partially explained by the relatively lack of knowledge that we still have regarding the molecular mechanisms underlying them, as well as by the complexity of their etiopathology. In fact, a complex number of changes in the physiological function of the cell has been described in all these aging-associated pathologies, including neurodegenerative disorders. Based on multiple scientific manuscripts produced by us and others, it seems clear that mitochondria are dysfunctional in many of these aging-associated pathologies. For example, mitochondrial dysfunction is an early event in the etiopathology of all the main neurodegenerative disorders, and it could be a trigger of many of the other deleterious changes which are present at the cellular level in these pathologies. While mitochondria are complex organelles and their regulation is still not yet entirely understood, inorganic polyphosphate (polyP) could play a crucial role in the regulation of some mitochondrial processes, which are dysfunctional in neurodegeneration. PolyP is a well-preserved biopolymer; it has been identified in every organism that has been studied. It is constituted by a series of orthophosphates connected by highly energetic phosphoanhydride bonds, comparable to those found in ATP. The literature suggests that the role of polyP in maintaining mitochondrial physiology might be related, at least partially, to its effects as a key regulator of cellular bioenergetics. However, further research needs to be conducted to fully elucidate the molecular mechanisms underlying the effects of polyP in the regulation of mitochondrial physiology in aging-associated pathologies, including neurodegenerative disorders. With a significant lack of therapeutic options for the prevention and/or treatment of neurodegeneration, the search for new pharmacological tools against these conditions has been continuous in past decades, even though very few therapeutic approaches have shown potential in treating these pathologies. Therefore, increasing our knowledge about the molecular mechanisms underlying the effects of polyP in mitochondrial physiology as well as its metabolism could place this polymer as a promising and innovative pharmacological target not only in neurodegeneration, but also in a wide range of aging-associated pathologies and conditions where mitochondrial dysfunction has been described as a crucial component of its etiopathology, such as diabetes, musculoskeletal disorders, and cardiovascular disorders.

摘要

随着人口老龄化,预计未来几十年内与衰老相关的疾病将增加。遗憾的是,我们仍然没有任何有效的药物或非药物手段来预防、逆转或治愈这些疾病。针对与衰老相关的疾病缺乏治疗方法的原因至少可以部分解释为,我们对其潜在的分子机制仍然知之甚少,以及其发病机制的复杂性。事实上,在所有这些与衰老相关的疾病中,包括神经退行性疾病,都已经描述了细胞生理功能的一系列复杂变化。基于我们和其他人撰写的多篇科学论文,似乎很清楚,线粒体在许多与衰老相关的疾病中都存在功能障碍。例如,线粒体功能障碍是所有主要神经退行性疾病发病机制中的早期事件,它可能是这些疾病中细胞水平上存在的许多其他有害变化的触发因素。虽然线粒体是复杂的细胞器,其调节机制尚未完全理解,但无机多磷酸盐(polyP)可能在调节一些线粒体功能方面发挥关键作用,而这些功能在神经退行性变中是失调的。polyP 是一种保存完好的生物聚合物,在所有已研究的生物体中都有发现。它由一系列通过高能磷酸酐键连接的正磷酸盐组成,类似于在 ATP 中发现的键。文献表明,polyP 在维持线粒体生理功能方面的作用可能与其作为细胞生物能量关键调节剂的作用至少部分相关。然而,为了充分阐明 polyP 在调节与衰老相关的疾病(包括神经退行性疾病)中线粒体生理的分子机制,还需要进一步研究。由于预防和/或治疗神经退行性疾病的治疗选择非常有限,过去几十年来,人们一直在不断寻找针对这些疾病的新药物治疗方法,尽管只有很少的治疗方法显示出对这些疾病有潜在疗效。因此,增加我们对 polyP 在调节线粒体生理及其代谢方面的分子机制的了解,可能使这种聚合物不仅成为神经退行性疾病的有前途和创新的药物治疗靶点,而且还可能成为广泛的与衰老相关的疾病和病症的药物治疗靶点,这些疾病和病症的发病机制中已经描述了线粒体功能障碍是其关键组成部分,如糖尿病、肌肉骨骼疾病和心血管疾病。

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