Cargando…
Suppression of PFKFB3-driven glycolysis restrains endothelial-to-mesenchymal transition and fibrotic response
Endothelial-to-mesenchymal transition (EndoMT), the process wherein endothelial cells lose endothelial identity and adopt mesenchymal-like phenotypes, constitutes a critical contributor to cardiac fibrosis. The phenotypic plasticity of endothelial cells can be intricately shaped by alteration of met...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433407/ https://www.ncbi.nlm.nih.gov/pubmed/36045132 http://dx.doi.org/10.1038/s41392-022-01097-6 |
_version_ | 1784780626151342080 |
---|---|
author | Zeng, Hao Pan, Ting Zhan, Meiling Hailiwu, Renaguli Liu, Baolin Yang, Hua Li, Ping |
author_facet | Zeng, Hao Pan, Ting Zhan, Meiling Hailiwu, Renaguli Liu, Baolin Yang, Hua Li, Ping |
author_sort | Zeng, Hao |
collection | PubMed |
description | Endothelial-to-mesenchymal transition (EndoMT), the process wherein endothelial cells lose endothelial identity and adopt mesenchymal-like phenotypes, constitutes a critical contributor to cardiac fibrosis. The phenotypic plasticity of endothelial cells can be intricately shaped by alteration of metabolic pathways, but how endothelial cells adjust cellular metabolism to drive EndoMT is incompletely understood. Here, we identified 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 (PFKFB3) as a critical driver of EndoMT via triggering abnormal glycolysis and compromising mitochondrial respiration. Pharmacological suppression of PFKFB3 with salvianolic acid C (SAC), a phenolic compound derived from Salvia miltiorrhiza, attenuates EndoMT and fibrotic response. PFKFB3-haplodeficiency recapitulates the anti-EndoMT effect of SAC while PFKFB3-overexpression augments the magnitude of EndoMT and exacerbates cardiac fibrosis. Mechanistically, PFKFB3-driven glycolysis compromises cytoplasmic nicotinamide adenine dinucleotide phosphate (reduced form, NADPH) production via hijacking glucose flux from pentose phosphate pathway. Efflux of mitochondrial NADPH through isocitrate/α-ketoglutarate shuttle replenishes cytoplasmic NADPH pool but meanwhile impairs mitochondrial respiration by hampering mitochondrial iron-sulfur cluster biosynthesis. SAC disrupts PFKFB3 stability by accelerating its degradation and thus maintains metabolic homeostasis in endothelial cells, underlying its anti-EndoMT effects. These findings for the first time identify the critical role of PFKFB3 in triggering EndoMT by driving abnormal glycolysis in endothelial cells, and also highlight the therapeutic potential for pharmacological intervention of PFKFB3 (with SAC or other PFKFB3 inhibitors) to combat EndoMT-associated fibrotic responses via metabolic regulation. |
format | Online Article Text |
id | pubmed-9433407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94334072022-09-02 Suppression of PFKFB3-driven glycolysis restrains endothelial-to-mesenchymal transition and fibrotic response Zeng, Hao Pan, Ting Zhan, Meiling Hailiwu, Renaguli Liu, Baolin Yang, Hua Li, Ping Signal Transduct Target Ther Article Endothelial-to-mesenchymal transition (EndoMT), the process wherein endothelial cells lose endothelial identity and adopt mesenchymal-like phenotypes, constitutes a critical contributor to cardiac fibrosis. The phenotypic plasticity of endothelial cells can be intricately shaped by alteration of metabolic pathways, but how endothelial cells adjust cellular metabolism to drive EndoMT is incompletely understood. Here, we identified 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 (PFKFB3) as a critical driver of EndoMT via triggering abnormal glycolysis and compromising mitochondrial respiration. Pharmacological suppression of PFKFB3 with salvianolic acid C (SAC), a phenolic compound derived from Salvia miltiorrhiza, attenuates EndoMT and fibrotic response. PFKFB3-haplodeficiency recapitulates the anti-EndoMT effect of SAC while PFKFB3-overexpression augments the magnitude of EndoMT and exacerbates cardiac fibrosis. Mechanistically, PFKFB3-driven glycolysis compromises cytoplasmic nicotinamide adenine dinucleotide phosphate (reduced form, NADPH) production via hijacking glucose flux from pentose phosphate pathway. Efflux of mitochondrial NADPH through isocitrate/α-ketoglutarate shuttle replenishes cytoplasmic NADPH pool but meanwhile impairs mitochondrial respiration by hampering mitochondrial iron-sulfur cluster biosynthesis. SAC disrupts PFKFB3 stability by accelerating its degradation and thus maintains metabolic homeostasis in endothelial cells, underlying its anti-EndoMT effects. These findings for the first time identify the critical role of PFKFB3 in triggering EndoMT by driving abnormal glycolysis in endothelial cells, and also highlight the therapeutic potential for pharmacological intervention of PFKFB3 (with SAC or other PFKFB3 inhibitors) to combat EndoMT-associated fibrotic responses via metabolic regulation. Nature Publishing Group UK 2022-09-01 /pmc/articles/PMC9433407/ /pubmed/36045132 http://dx.doi.org/10.1038/s41392-022-01097-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zeng, Hao Pan, Ting Zhan, Meiling Hailiwu, Renaguli Liu, Baolin Yang, Hua Li, Ping Suppression of PFKFB3-driven glycolysis restrains endothelial-to-mesenchymal transition and fibrotic response |
title | Suppression of PFKFB3-driven glycolysis restrains endothelial-to-mesenchymal transition and fibrotic response |
title_full | Suppression of PFKFB3-driven glycolysis restrains endothelial-to-mesenchymal transition and fibrotic response |
title_fullStr | Suppression of PFKFB3-driven glycolysis restrains endothelial-to-mesenchymal transition and fibrotic response |
title_full_unstemmed | Suppression of PFKFB3-driven glycolysis restrains endothelial-to-mesenchymal transition and fibrotic response |
title_short | Suppression of PFKFB3-driven glycolysis restrains endothelial-to-mesenchymal transition and fibrotic response |
title_sort | suppression of pfkfb3-driven glycolysis restrains endothelial-to-mesenchymal transition and fibrotic response |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433407/ https://www.ncbi.nlm.nih.gov/pubmed/36045132 http://dx.doi.org/10.1038/s41392-022-01097-6 |
work_keys_str_mv | AT zenghao suppressionofpfkfb3drivenglycolysisrestrainsendothelialtomesenchymaltransitionandfibroticresponse AT panting suppressionofpfkfb3drivenglycolysisrestrainsendothelialtomesenchymaltransitionandfibroticresponse AT zhanmeiling suppressionofpfkfb3drivenglycolysisrestrainsendothelialtomesenchymaltransitionandfibroticresponse AT hailiwurenaguli suppressionofpfkfb3drivenglycolysisrestrainsendothelialtomesenchymaltransitionandfibroticresponse AT liubaolin suppressionofpfkfb3drivenglycolysisrestrainsendothelialtomesenchymaltransitionandfibroticresponse AT yanghua suppressionofpfkfb3drivenglycolysisrestrainsendothelialtomesenchymaltransitionandfibroticresponse AT liping suppressionofpfkfb3drivenglycolysisrestrainsendothelialtomesenchymaltransitionandfibroticresponse |