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Ahnak depletion accelerates liver regeneration by modulating the TGF-β/Smad signaling pathway

Ahnak, a large protein first identified as an inhibitor of TGF-β signaling in human neuroblastoma, was recently shown to promote TGF-β in some cancers. The TGF-β signaling pathway regulates cell growth, various biological functions, and cancer growth and metastasis. In this study, we used Ahnak knoc...

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Autores principales: Yang, Insook, Son, Yeri, Shin, Jae Hoon, Kim, Il Yong, Seong, Je Kyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Biochemistry and Molecular Biology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442348/
https://www.ncbi.nlm.nih.gov/pubmed/35880432
http://dx.doi.org/10.5483/BMBRep.2022.55.8.071
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author Yang, Insook
Son, Yeri
Shin, Jae Hoon
Kim, Il Yong
Seong, Je Kyung
author_facet Yang, Insook
Son, Yeri
Shin, Jae Hoon
Kim, Il Yong
Seong, Je Kyung
author_sort Yang, Insook
collection PubMed
description Ahnak, a large protein first identified as an inhibitor of TGF-β signaling in human neuroblastoma, was recently shown to promote TGF-β in some cancers. The TGF-β signaling pathway regulates cell growth, various biological functions, and cancer growth and metastasis. In this study, we used Ahnak knockout (KO) mice that underwent a 70% partial hepatectomy (PH) to investigate the function of Ahnak in TGF-β signaling during liver regeneration. At the indicated time points after PH, we analyzed the mRNA and protein expression of the TGF -β/Smad signaling pathway and cell cycle-related factors, evaluated the cell cycle through proliferating cell nuclear antigen (PCNA) immunostai-ning, analyzed the mitotic index by hematoxylin and eosin staining. We also measured the ratio of liver tissue weight to body weight. Activation of TGF-β signaling was confirmed by analyzing the levels of phospho-Smad 2 and 3 in the liver at the indicated time points after PH and was lower in Ahnak KO mice than in WT mice. The expression levels of cyclin B1, D1, and E1; proteins in the Rb/E2F transcriptional pathway, which regulates the cell cycle; and the numbers of PCNA-positive cells were increased in Ahnak KO mice and showed tendencies opposite that of TGF-β expression. During postoperative regeneration, the liver weight to body weight ratio tended to increase faster in Ahnak KO mice. However, 7 days after PH, both groups of mice showed similar rates of regeneration, following which their active regeneration stopped. Analysis of hepatocytes undergoing mitosis showed that there were more mitotic cells in Ahnak KO mice, consistent with the weight ratio. Our findings suggest that Ahnak enhances TGF-β signaling during postoperative liver regeneration, resulting in cell cycle disruption; this highlights a novel role of Ahnak in liver regeneration. These results provide new insight into liver regeneration and potential treatment targets for liver diseases that require surgical treatment.
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spelling pubmed-94423482022-09-12 Ahnak depletion accelerates liver regeneration by modulating the TGF-β/Smad signaling pathway Yang, Insook Son, Yeri Shin, Jae Hoon Kim, Il Yong Seong, Je Kyung BMB Rep Article Ahnak, a large protein first identified as an inhibitor of TGF-β signaling in human neuroblastoma, was recently shown to promote TGF-β in some cancers. The TGF-β signaling pathway regulates cell growth, various biological functions, and cancer growth and metastasis. In this study, we used Ahnak knockout (KO) mice that underwent a 70% partial hepatectomy (PH) to investigate the function of Ahnak in TGF-β signaling during liver regeneration. At the indicated time points after PH, we analyzed the mRNA and protein expression of the TGF -β/Smad signaling pathway and cell cycle-related factors, evaluated the cell cycle through proliferating cell nuclear antigen (PCNA) immunostai-ning, analyzed the mitotic index by hematoxylin and eosin staining. We also measured the ratio of liver tissue weight to body weight. Activation of TGF-β signaling was confirmed by analyzing the levels of phospho-Smad 2 and 3 in the liver at the indicated time points after PH and was lower in Ahnak KO mice than in WT mice. The expression levels of cyclin B1, D1, and E1; proteins in the Rb/E2F transcriptional pathway, which regulates the cell cycle; and the numbers of PCNA-positive cells were increased in Ahnak KO mice and showed tendencies opposite that of TGF-β expression. During postoperative regeneration, the liver weight to body weight ratio tended to increase faster in Ahnak KO mice. However, 7 days after PH, both groups of mice showed similar rates of regeneration, following which their active regeneration stopped. Analysis of hepatocytes undergoing mitosis showed that there were more mitotic cells in Ahnak KO mice, consistent with the weight ratio. Our findings suggest that Ahnak enhances TGF-β signaling during postoperative liver regeneration, resulting in cell cycle disruption; this highlights a novel role of Ahnak in liver regeneration. These results provide new insight into liver regeneration and potential treatment targets for liver diseases that require surgical treatment. Korean Society for Biochemistry and Molecular Biology 2022-08-31 2022-08-31 /pmc/articles/PMC9442348/ /pubmed/35880432 http://dx.doi.org/10.5483/BMBRep.2022.55.8.071 Text en Copyright © 2022 by the The Korean Society for Biochemistry and Molecular Biology https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Yang, Insook
Son, Yeri
Shin, Jae Hoon
Kim, Il Yong
Seong, Je Kyung
Ahnak depletion accelerates liver regeneration by modulating the TGF-β/Smad signaling pathway
title Ahnak depletion accelerates liver regeneration by modulating the TGF-β/Smad signaling pathway
title_full Ahnak depletion accelerates liver regeneration by modulating the TGF-β/Smad signaling pathway
title_fullStr Ahnak depletion accelerates liver regeneration by modulating the TGF-β/Smad signaling pathway
title_full_unstemmed Ahnak depletion accelerates liver regeneration by modulating the TGF-β/Smad signaling pathway
title_short Ahnak depletion accelerates liver regeneration by modulating the TGF-β/Smad signaling pathway
title_sort ahnak depletion accelerates liver regeneration by modulating the tgf-β/smad signaling pathway
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442348/
https://www.ncbi.nlm.nih.gov/pubmed/35880432
http://dx.doi.org/10.5483/BMBRep.2022.55.8.071
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