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Lactylation, a Novel Metabolic Reprogramming Code: Current Status and Prospects
Lactate is an end product of glycolysis. As a critical energy source for mitochondrial respiration, lactate also acts as a precursor of gluconeogenesis and a signaling molecule. We briefly summarize emerging concepts regarding lactate metabolism, such as the lactate shuttle, lactate homeostasis, and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8222712/ https://www.ncbi.nlm.nih.gov/pubmed/34177945 http://dx.doi.org/10.3389/fimmu.2021.688910 |
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author | Chen, An-Na Luo, Yan Yang, Yu-Han Fu, Jian-Tao Geng, Xiu-Mei Shi, Jun-Ping Yang, Jin |
author_facet | Chen, An-Na Luo, Yan Yang, Yu-Han Fu, Jian-Tao Geng, Xiu-Mei Shi, Jun-Ping Yang, Jin |
author_sort | Chen, An-Na |
collection | PubMed |
description | Lactate is an end product of glycolysis. As a critical energy source for mitochondrial respiration, lactate also acts as a precursor of gluconeogenesis and a signaling molecule. We briefly summarize emerging concepts regarding lactate metabolism, such as the lactate shuttle, lactate homeostasis, and lactate-microenvironment interaction. Accumulating evidence indicates that lactate-mediated reprogramming of immune cells and enhancement of cellular plasticity contribute to establishing disease-specific immunity status. However, the mechanisms by which changes in lactate states influence the establishment of diverse functional adaptive states are largely uncharacterized. Posttranslational histone modifications create a code that functions as a key sensor of metabolism and are responsible for transducing metabolic changes into stable gene expression patterns. In this review, we describe the recent advances in a novel lactate-induced histone modification, histone lysine lactylation. These observations support the idea that epigenetic reprogramming-linked lactate input is related to disease state outputs, such as cancer progression and drug resistance. |
format | Online Article Text |
id | pubmed-8222712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82227122021-06-25 Lactylation, a Novel Metabolic Reprogramming Code: Current Status and Prospects Chen, An-Na Luo, Yan Yang, Yu-Han Fu, Jian-Tao Geng, Xiu-Mei Shi, Jun-Ping Yang, Jin Front Immunol Immunology Lactate is an end product of glycolysis. As a critical energy source for mitochondrial respiration, lactate also acts as a precursor of gluconeogenesis and a signaling molecule. We briefly summarize emerging concepts regarding lactate metabolism, such as the lactate shuttle, lactate homeostasis, and lactate-microenvironment interaction. Accumulating evidence indicates that lactate-mediated reprogramming of immune cells and enhancement of cellular plasticity contribute to establishing disease-specific immunity status. However, the mechanisms by which changes in lactate states influence the establishment of diverse functional adaptive states are largely uncharacterized. Posttranslational histone modifications create a code that functions as a key sensor of metabolism and are responsible for transducing metabolic changes into stable gene expression patterns. In this review, we describe the recent advances in a novel lactate-induced histone modification, histone lysine lactylation. These observations support the idea that epigenetic reprogramming-linked lactate input is related to disease state outputs, such as cancer progression and drug resistance. Frontiers Media S.A. 2021-06-10 /pmc/articles/PMC8222712/ /pubmed/34177945 http://dx.doi.org/10.3389/fimmu.2021.688910 Text en Copyright © 2021 Chen, Luo, Yang, Fu, Geng, Shi and Yang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Chen, An-Na Luo, Yan Yang, Yu-Han Fu, Jian-Tao Geng, Xiu-Mei Shi, Jun-Ping Yang, Jin Lactylation, a Novel Metabolic Reprogramming Code: Current Status and Prospects |
title | Lactylation, a Novel Metabolic Reprogramming Code: Current Status and Prospects |
title_full | Lactylation, a Novel Metabolic Reprogramming Code: Current Status and Prospects |
title_fullStr | Lactylation, a Novel Metabolic Reprogramming Code: Current Status and Prospects |
title_full_unstemmed | Lactylation, a Novel Metabolic Reprogramming Code: Current Status and Prospects |
title_short | Lactylation, a Novel Metabolic Reprogramming Code: Current Status and Prospects |
title_sort | lactylation, a novel metabolic reprogramming code: current status and prospects |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8222712/ https://www.ncbi.nlm.nih.gov/pubmed/34177945 http://dx.doi.org/10.3389/fimmu.2021.688910 |
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