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Antimicrobial Peptides Mediate Apoptosis by Changing Mitochondrial Membrane Permeability

Changes in mitochondrial membrane permeability are closely associated with mitochondria-mediated apoptosis. Antimicrobial peptides (AMPs), which have been found to enter cells to exert physiological effects, cause damage to the mitochondria. This paper reviews the molecular mechanisms of AMP-mediate...

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Autores principales: Wang, Hongji, Zhang, Chaowen, Li, Mengnan, Liu, Chaoran, Wang, Jingyi, Ou, Xuan, Han, Yuzhu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653759/
https://www.ncbi.nlm.nih.gov/pubmed/36361521
http://dx.doi.org/10.3390/ijms232112732
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author Wang, Hongji
Zhang, Chaowen
Li, Mengnan
Liu, Chaoran
Wang, Jingyi
Ou, Xuan
Han, Yuzhu
author_facet Wang, Hongji
Zhang, Chaowen
Li, Mengnan
Liu, Chaoran
Wang, Jingyi
Ou, Xuan
Han, Yuzhu
author_sort Wang, Hongji
collection PubMed
description Changes in mitochondrial membrane permeability are closely associated with mitochondria-mediated apoptosis. Antimicrobial peptides (AMPs), which have been found to enter cells to exert physiological effects, cause damage to the mitochondria. This paper reviews the molecular mechanisms of AMP-mediated apoptosis by changing the permeability of the mitochondrial membrane through three pathways: the outer mitochondrial membrane (OMM), inner mitochondrial membrane (IMM), and mitochondrial permeability transition pore (MPTP). The roles of AMPs in inducing changes in membrane permeability and apoptosis are also discussed. Combined with recent research results, the possible application prospects of AMPs are proposed to provide a theoretical reference for the development of AMPs as therapeutic agents for human diseases.
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spelling pubmed-96537592022-11-15 Antimicrobial Peptides Mediate Apoptosis by Changing Mitochondrial Membrane Permeability Wang, Hongji Zhang, Chaowen Li, Mengnan Liu, Chaoran Wang, Jingyi Ou, Xuan Han, Yuzhu Int J Mol Sci Review Changes in mitochondrial membrane permeability are closely associated with mitochondria-mediated apoptosis. Antimicrobial peptides (AMPs), which have been found to enter cells to exert physiological effects, cause damage to the mitochondria. This paper reviews the molecular mechanisms of AMP-mediated apoptosis by changing the permeability of the mitochondrial membrane through three pathways: the outer mitochondrial membrane (OMM), inner mitochondrial membrane (IMM), and mitochondrial permeability transition pore (MPTP). The roles of AMPs in inducing changes in membrane permeability and apoptosis are also discussed. Combined with recent research results, the possible application prospects of AMPs are proposed to provide a theoretical reference for the development of AMPs as therapeutic agents for human diseases. MDPI 2022-10-22 /pmc/articles/PMC9653759/ /pubmed/36361521 http://dx.doi.org/10.3390/ijms232112732 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wang, Hongji
Zhang, Chaowen
Li, Mengnan
Liu, Chaoran
Wang, Jingyi
Ou, Xuan
Han, Yuzhu
Antimicrobial Peptides Mediate Apoptosis by Changing Mitochondrial Membrane Permeability
title Antimicrobial Peptides Mediate Apoptosis by Changing Mitochondrial Membrane Permeability
title_full Antimicrobial Peptides Mediate Apoptosis by Changing Mitochondrial Membrane Permeability
title_fullStr Antimicrobial Peptides Mediate Apoptosis by Changing Mitochondrial Membrane Permeability
title_full_unstemmed Antimicrobial Peptides Mediate Apoptosis by Changing Mitochondrial Membrane Permeability
title_short Antimicrobial Peptides Mediate Apoptosis by Changing Mitochondrial Membrane Permeability
title_sort antimicrobial peptides mediate apoptosis by changing mitochondrial membrane permeability
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653759/
https://www.ncbi.nlm.nih.gov/pubmed/36361521
http://dx.doi.org/10.3390/ijms232112732
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