Inorganic Polyphosphate, Mitochondria, and Neurodegeneration.

Aging Bioenergetics Inorganic polyphosphate Mitochondrial dysfunction Mitochondrial permeability transition pore Mitochondrial unfolded protein response Neurodegeneration Oxidative phosphorylation PolyP Stress response

Journal

Progress in molecular and subcellular biology
ISSN: 0079-6484
Titre abrégé: Prog Mol Subcell Biol
Pays: United States
ID NLM: 0233223

Informations de publication

Date de publication:
2022
Historique:
entrez: 13 6 2022
pubmed: 14 6 2022
medline: 16 6 2022
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 35697936
doi: 10.1007/978-3-031-01237-2_3
doi:

Substances chimiques

Polyphosphates 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

27-49

Subventions

Organisme : NIA NIH HHS
ID : R00 AG055701
Pays : United States

Informations de copyright

© 2022. The Author(s), under exclusive license to Springer Nature Switzerland AG.

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Auteurs

Pedro Urquiza (P)

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

Maria E Solesio (ME)

Department of Biology, Rutgers University, Camden, NJ, USA. m.solesio@rutgers.edu.

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