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Comparative studies of the expression of creatine kinase isoforms under immune stress in Pelodiscus sinensis
The expression and localization of different isoforms of creatine kinase in Pelodiscus sinensis (PSCK) were studied to reveal the role of PSCK isozymes (PSCK-B, PSCK-M, PSCK-S) under bacterial infection-induced immunologic stress. The computational molecular dynamics simulations predicted that PSCK-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282771/ https://www.ncbi.nlm.nih.gov/pubmed/32531365 http://dx.doi.org/10.1016/j.ijbiomac.2020.06.036 |
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author | Li, Caiyan Wang, Wei Lee, Jinhyuk Zeng, Lifang Yang, Yufei Yin, Shang-Jun Park, Yong-Doo Qian, Guo-Ying |
author_facet | Li, Caiyan Wang, Wei Lee, Jinhyuk Zeng, Lifang Yang, Yufei Yin, Shang-Jun Park, Yong-Doo Qian, Guo-Ying |
author_sort | Li, Caiyan |
collection | PubMed |
description | The expression and localization of different isoforms of creatine kinase in Pelodiscus sinensis (PSCK) were studied to reveal the role of PSCK isozymes (PSCK-B, PSCK-M, PSCK-S) under bacterial infection-induced immunologic stress. The computational molecular dynamics simulations predicted that PSCK-S would mostly possess a kinase function in a structural aspect when compared to PSCK-B and PSCK-M. The assay of biochemical parameters such as total superoxide dismutase (T-SOD), lactate dehydrogenase (LDH), malondialdehyde (MDA), catalase (CAT), and the content of ATP were measured along with total PSCK activity in different tissue samples under bacterial infection. The expression detections of PSCK isozymes in vitro and in vivo were overall well-matched where PSCK isozymes were expressed differently in P. sinensis tissues. The results showed that PSCK-B mostly contributes to the spleen, followed by the liver and myocardium; PSCK-M mostly contributes to the liver, followed by the myocardium and skeletal muscle, while PSCK-S contributes to the spleen and is uniquely expressed in skeletal muscle. Our study suggests that the various alterations of PSCK isozymes in tissues of P. sinensis are prone to defense the bacterial infection and blocking energetic imbalance before severe pathogenesis turned on in P. sinensis. |
format | Online Article Text |
id | pubmed-7282771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72827712020-06-10 Comparative studies of the expression of creatine kinase isoforms under immune stress in Pelodiscus sinensis Li, Caiyan Wang, Wei Lee, Jinhyuk Zeng, Lifang Yang, Yufei Yin, Shang-Jun Park, Yong-Doo Qian, Guo-Ying Int J Biol Macromol Article The expression and localization of different isoforms of creatine kinase in Pelodiscus sinensis (PSCK) were studied to reveal the role of PSCK isozymes (PSCK-B, PSCK-M, PSCK-S) under bacterial infection-induced immunologic stress. The computational molecular dynamics simulations predicted that PSCK-S would mostly possess a kinase function in a structural aspect when compared to PSCK-B and PSCK-M. The assay of biochemical parameters such as total superoxide dismutase (T-SOD), lactate dehydrogenase (LDH), malondialdehyde (MDA), catalase (CAT), and the content of ATP were measured along with total PSCK activity in different tissue samples under bacterial infection. The expression detections of PSCK isozymes in vitro and in vivo were overall well-matched where PSCK isozymes were expressed differently in P. sinensis tissues. The results showed that PSCK-B mostly contributes to the spleen, followed by the liver and myocardium; PSCK-M mostly contributes to the liver, followed by the myocardium and skeletal muscle, while PSCK-S contributes to the spleen and is uniquely expressed in skeletal muscle. Our study suggests that the various alterations of PSCK isozymes in tissues of P. sinensis are prone to defense the bacterial infection and blocking energetic imbalance before severe pathogenesis turned on in P. sinensis. Elsevier B.V. 2020-11-01 2020-06-09 /pmc/articles/PMC7282771/ /pubmed/32531365 http://dx.doi.org/10.1016/j.ijbiomac.2020.06.036 Text en © 2020 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Li, Caiyan Wang, Wei Lee, Jinhyuk Zeng, Lifang Yang, Yufei Yin, Shang-Jun Park, Yong-Doo Qian, Guo-Ying Comparative studies of the expression of creatine kinase isoforms under immune stress in Pelodiscus sinensis |
title | Comparative studies of the expression of creatine kinase isoforms under immune stress in Pelodiscus sinensis |
title_full | Comparative studies of the expression of creatine kinase isoforms under immune stress in Pelodiscus sinensis |
title_fullStr | Comparative studies of the expression of creatine kinase isoforms under immune stress in Pelodiscus sinensis |
title_full_unstemmed | Comparative studies of the expression of creatine kinase isoforms under immune stress in Pelodiscus sinensis |
title_short | Comparative studies of the expression of creatine kinase isoforms under immune stress in Pelodiscus sinensis |
title_sort | comparative studies of the expression of creatine kinase isoforms under immune stress in pelodiscus sinensis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282771/ https://www.ncbi.nlm.nih.gov/pubmed/32531365 http://dx.doi.org/10.1016/j.ijbiomac.2020.06.036 |
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