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The pseudoenzyme ADPRHL1 affects cardiac function by regulating the ROCK pathway
BACKGROUND: Pseudoenzymes, catalytically deficient variants of active enzymes, have a wide range of regulatory functions. ADP-ribosylhydrolase-like 1 (ADPRHL1), a pseudoenzyme belonging to a small group of ADP-ribosylhydrolase enzymes that lacks the amino acid residues necessary for catalytic activi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601310/ https://www.ncbi.nlm.nih.gov/pubmed/37880701 http://dx.doi.org/10.1186/s13287-023-03507-0 |
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author | Tian, Lei Guo, Tianwei Wu, Fujian Bai, Rui Ai, Sinan Wang, Hongyue Song, Yuanxiu Zhu, Min Jiang, Youxu Ma, Shuhong Zhuang, Xiaofeng Guo, Shuzhen |
author_facet | Tian, Lei Guo, Tianwei Wu, Fujian Bai, Rui Ai, Sinan Wang, Hongyue Song, Yuanxiu Zhu, Min Jiang, Youxu Ma, Shuhong Zhuang, Xiaofeng Guo, Shuzhen |
author_sort | Tian, Lei |
collection | PubMed |
description | BACKGROUND: Pseudoenzymes, catalytically deficient variants of active enzymes, have a wide range of regulatory functions. ADP-ribosylhydrolase-like 1 (ADPRHL1), a pseudoenzyme belonging to a small group of ADP-ribosylhydrolase enzymes that lacks the amino acid residues necessary for catalytic activity, may have a significant role in heart development based on accumulating evidence. However, the specific function of ADPRHL1 in this process has not been elucidated. To investigate the role of ADPRHL1 in the heart, we generated the first in vitro human embryonic stem cell model with an ADPRHL1 knockout. METHOD: Using the CRISPR/Cas9 system, we generated ADPRHL1 knockout in the human embryonic stem cell (hESC) H9 line. The cells were differentiated into cardiomyocytes using a chemically defined and xeno-free method. We employed confocal laser microscopy to detect calcium transients and microelectrode array (MEA) to assess the electrophysiological activity of ADPRHL1 deficiency cardiomyocytes. Additionally, we investigated the cellular mechanism of ADPRHL1 by Bulk RNA sequencing and western blot. RESULTS: The results indicate that the absence of ADPRHL1 in cardiomyocytes led to adhered abnormally, as well as perturbations in calcium transients and electrophysiological activity. We also revealed that disruption of focal adhesion formation in these cardiomyocytes was due to an excessive upregulation of the ROCK–myosin II pathway. Notably, inhibition of ROCK and myosin II effectively restores focal adhesions in ADPRHL1-deficient cardiomyocytes and improved electrical conduction and calcium activity. CONCLUSIONS: Our findings demonstrate that ADPRHL1 plays a critical role in maintaining the proper function of cardiomyocytes by regulating the ROCK–myosin II pathway, suggesting that it may serve as a potential drug target for the treatment of ADPRHL1-related diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03507-0. |
format | Online Article Text |
id | pubmed-10601310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106013102023-10-27 The pseudoenzyme ADPRHL1 affects cardiac function by regulating the ROCK pathway Tian, Lei Guo, Tianwei Wu, Fujian Bai, Rui Ai, Sinan Wang, Hongyue Song, Yuanxiu Zhu, Min Jiang, Youxu Ma, Shuhong Zhuang, Xiaofeng Guo, Shuzhen Stem Cell Res Ther Research BACKGROUND: Pseudoenzymes, catalytically deficient variants of active enzymes, have a wide range of regulatory functions. ADP-ribosylhydrolase-like 1 (ADPRHL1), a pseudoenzyme belonging to a small group of ADP-ribosylhydrolase enzymes that lacks the amino acid residues necessary for catalytic activity, may have a significant role in heart development based on accumulating evidence. However, the specific function of ADPRHL1 in this process has not been elucidated. To investigate the role of ADPRHL1 in the heart, we generated the first in vitro human embryonic stem cell model with an ADPRHL1 knockout. METHOD: Using the CRISPR/Cas9 system, we generated ADPRHL1 knockout in the human embryonic stem cell (hESC) H9 line. The cells were differentiated into cardiomyocytes using a chemically defined and xeno-free method. We employed confocal laser microscopy to detect calcium transients and microelectrode array (MEA) to assess the electrophysiological activity of ADPRHL1 deficiency cardiomyocytes. Additionally, we investigated the cellular mechanism of ADPRHL1 by Bulk RNA sequencing and western blot. RESULTS: The results indicate that the absence of ADPRHL1 in cardiomyocytes led to adhered abnormally, as well as perturbations in calcium transients and electrophysiological activity. We also revealed that disruption of focal adhesion formation in these cardiomyocytes was due to an excessive upregulation of the ROCK–myosin II pathway. Notably, inhibition of ROCK and myosin II effectively restores focal adhesions in ADPRHL1-deficient cardiomyocytes and improved electrical conduction and calcium activity. CONCLUSIONS: Our findings demonstrate that ADPRHL1 plays a critical role in maintaining the proper function of cardiomyocytes by regulating the ROCK–myosin II pathway, suggesting that it may serve as a potential drug target for the treatment of ADPRHL1-related diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03507-0. BioMed Central 2023-10-26 /pmc/articles/PMC10601310/ /pubmed/37880701 http://dx.doi.org/10.1186/s13287-023-03507-0 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Tian, Lei Guo, Tianwei Wu, Fujian Bai, Rui Ai, Sinan Wang, Hongyue Song, Yuanxiu Zhu, Min Jiang, Youxu Ma, Shuhong Zhuang, Xiaofeng Guo, Shuzhen The pseudoenzyme ADPRHL1 affects cardiac function by regulating the ROCK pathway |
title | The pseudoenzyme ADPRHL1 affects cardiac function by regulating the ROCK pathway |
title_full | The pseudoenzyme ADPRHL1 affects cardiac function by regulating the ROCK pathway |
title_fullStr | The pseudoenzyme ADPRHL1 affects cardiac function by regulating the ROCK pathway |
title_full_unstemmed | The pseudoenzyme ADPRHL1 affects cardiac function by regulating the ROCK pathway |
title_short | The pseudoenzyme ADPRHL1 affects cardiac function by regulating the ROCK pathway |
title_sort | pseudoenzyme adprhl1 affects cardiac function by regulating the rock pathway |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601310/ https://www.ncbi.nlm.nih.gov/pubmed/37880701 http://dx.doi.org/10.1186/s13287-023-03507-0 |
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