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GSK3β Inhibition Ameliorates Atherosclerotic Calcification

Endothelial-mesenchymal transition (EndMT) drives endothelium to contribute to atherosclerotic calcification. In a previous study, we showed that glycogen synthase kinase-3β (GSK3β) inhibition induced β-catenin and reduced mothers against DPP homolog 1 (SMAD1) in order to redirect osteoblast-like ce...

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Autores principales: Cai, Xinjiang, Zhao, Yan, Yang, Yang, Wu, Xiuju, Zhang, Li, Ma, Jocelyn A., Ji, Jaden, Boström, Kristina I., Yao, Yucheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10380320/
https://www.ncbi.nlm.nih.gov/pubmed/37511396
http://dx.doi.org/10.3390/ijms241411638
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author Cai, Xinjiang
Zhao, Yan
Yang, Yang
Wu, Xiuju
Zhang, Li
Ma, Jocelyn A.
Ji, Jaden
Boström, Kristina I.
Yao, Yucheng
author_facet Cai, Xinjiang
Zhao, Yan
Yang, Yang
Wu, Xiuju
Zhang, Li
Ma, Jocelyn A.
Ji, Jaden
Boström, Kristina I.
Yao, Yucheng
author_sort Cai, Xinjiang
collection PubMed
description Endothelial-mesenchymal transition (EndMT) drives endothelium to contribute to atherosclerotic calcification. In a previous study, we showed that glycogen synthase kinase-3β (GSK3β) inhibition induced β-catenin and reduced mothers against DPP homolog 1 (SMAD1) in order to redirect osteoblast-like cells towards endothelial lineage, thereby reducing vascular calcification in Matrix Gla Protein (Mgp) deficiency and diabetic Ins2(Akita/wt) mice. Here, we report that GSK3β inhibition or endothelial-specific deletion of GSK3β reduces atherosclerotic calcification. We also find that alterations in β-catenin and SMAD1 induced by GSK3β inhibition in the aortas of Apoe(−/−) mice are similar to Mgp(−/−) mice. Together, our results suggest that GSK3β inhibition reduces vascular calcification in atherosclerotic lesions through a similar mechanism to that in Mgp(−/−) mice.
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spelling pubmed-103803202023-07-29 GSK3β Inhibition Ameliorates Atherosclerotic Calcification Cai, Xinjiang Zhao, Yan Yang, Yang Wu, Xiuju Zhang, Li Ma, Jocelyn A. Ji, Jaden Boström, Kristina I. Yao, Yucheng Int J Mol Sci Communication Endothelial-mesenchymal transition (EndMT) drives endothelium to contribute to atherosclerotic calcification. In a previous study, we showed that glycogen synthase kinase-3β (GSK3β) inhibition induced β-catenin and reduced mothers against DPP homolog 1 (SMAD1) in order to redirect osteoblast-like cells towards endothelial lineage, thereby reducing vascular calcification in Matrix Gla Protein (Mgp) deficiency and diabetic Ins2(Akita/wt) mice. Here, we report that GSK3β inhibition or endothelial-specific deletion of GSK3β reduces atherosclerotic calcification. We also find that alterations in β-catenin and SMAD1 induced by GSK3β inhibition in the aortas of Apoe(−/−) mice are similar to Mgp(−/−) mice. Together, our results suggest that GSK3β inhibition reduces vascular calcification in atherosclerotic lesions through a similar mechanism to that in Mgp(−/−) mice. MDPI 2023-07-19 /pmc/articles/PMC10380320/ /pubmed/37511396 http://dx.doi.org/10.3390/ijms241411638 Text en © 2023 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 Communication
Cai, Xinjiang
Zhao, Yan
Yang, Yang
Wu, Xiuju
Zhang, Li
Ma, Jocelyn A.
Ji, Jaden
Boström, Kristina I.
Yao, Yucheng
GSK3β Inhibition Ameliorates Atherosclerotic Calcification
title GSK3β Inhibition Ameliorates Atherosclerotic Calcification
title_full GSK3β Inhibition Ameliorates Atherosclerotic Calcification
title_fullStr GSK3β Inhibition Ameliorates Atherosclerotic Calcification
title_full_unstemmed GSK3β Inhibition Ameliorates Atherosclerotic Calcification
title_short GSK3β Inhibition Ameliorates Atherosclerotic Calcification
title_sort gsk3β inhibition ameliorates atherosclerotic calcification
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10380320/
https://www.ncbi.nlm.nih.gov/pubmed/37511396
http://dx.doi.org/10.3390/ijms241411638
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