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Grape seed proanthocyanidin extract protects lymphocytes against histone-induced apoptosis

Apoptosis of lymphocytes is associated with immunosuppression and poor prognosis in sepsis. Our previous report showed that histones, nuclear proteins released from damaged or dying cells in sepsis, can mediate lymphocyte apoptosis via mitochondria damage. Grape seed proanthocyanidin extract (GSPE),...

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Autores principales: Chang, Ping, Mo, Bing, Cauvi, David M., Yu, Ying, Guo, Zhenhui, Zhou, Jian, Huang, Qiong, Yan, Qitao, Chen, Guiming, Liu, Zhanguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363264/
https://www.ncbi.nlm.nih.gov/pubmed/28344907
http://dx.doi.org/10.7717/peerj.3108
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author Chang, Ping
Mo, Bing
Cauvi, David M.
Yu, Ying
Guo, Zhenhui
Zhou, Jian
Huang, Qiong
Yan, Qitao
Chen, Guiming
Liu, Zhanguo
author_facet Chang, Ping
Mo, Bing
Cauvi, David M.
Yu, Ying
Guo, Zhenhui
Zhou, Jian
Huang, Qiong
Yan, Qitao
Chen, Guiming
Liu, Zhanguo
author_sort Chang, Ping
collection PubMed
description Apoptosis of lymphocytes is associated with immunosuppression and poor prognosis in sepsis. Our previous report showed that histones, nuclear proteins released from damaged or dying cells in sepsis, can mediate lymphocyte apoptosis via mitochondria damage. Grape seed proanthocyanidin extract (GSPE), a natural substance with protective properties against oxidative stress, plays a vital role in cell and mitochondria protection. We thus hypothesized that GSPE may play a protective role in histone-induced lymphocyte apoptosis through its anti-oxidative properties. In this study, we investigated the protective efficacy of GSPE on lymphocyte apoptosis induced by extracellular histones, a main contributor of death in sepsis. Human blood lymphocytes were treated with 50 μg/ml histones, 2 μg/ml GSPE, or a combination of both. A total of 100 μM N-acetylcysteine (NAC), a reactive oxygen species (ROS) inhibitor, was used as a positive control for GSPE. Apoptosis, intracellular ROS levels, mitochondrial membrane potential, Bcl-2 expression, and caspase-3 cleavage were measured. Our data clearly indicate that GSPE significantly inhibited lymphocyte apoptosis, generation of ROS, the loss of mitochondrial membrane potential, the decrease in Bcl-2 expression, and caspase-3 activation induced by extracellular histones. In conclusion, we show that GSPE has a protective effect on lymphocyte apoptosis induced by extracellular histones. This study suggests GSPE as a potential therapeutic agent that could help reduce lymphocyte apoptosis, and thus the state of immunosuppression was observed in septic patients.
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spelling pubmed-53632642017-03-24 Grape seed proanthocyanidin extract protects lymphocytes against histone-induced apoptosis Chang, Ping Mo, Bing Cauvi, David M. Yu, Ying Guo, Zhenhui Zhou, Jian Huang, Qiong Yan, Qitao Chen, Guiming Liu, Zhanguo PeerJ Cell Biology Apoptosis of lymphocytes is associated with immunosuppression and poor prognosis in sepsis. Our previous report showed that histones, nuclear proteins released from damaged or dying cells in sepsis, can mediate lymphocyte apoptosis via mitochondria damage. Grape seed proanthocyanidin extract (GSPE), a natural substance with protective properties against oxidative stress, plays a vital role in cell and mitochondria protection. We thus hypothesized that GSPE may play a protective role in histone-induced lymphocyte apoptosis through its anti-oxidative properties. In this study, we investigated the protective efficacy of GSPE on lymphocyte apoptosis induced by extracellular histones, a main contributor of death in sepsis. Human blood lymphocytes were treated with 50 μg/ml histones, 2 μg/ml GSPE, or a combination of both. A total of 100 μM N-acetylcysteine (NAC), a reactive oxygen species (ROS) inhibitor, was used as a positive control for GSPE. Apoptosis, intracellular ROS levels, mitochondrial membrane potential, Bcl-2 expression, and caspase-3 cleavage were measured. Our data clearly indicate that GSPE significantly inhibited lymphocyte apoptosis, generation of ROS, the loss of mitochondrial membrane potential, the decrease in Bcl-2 expression, and caspase-3 activation induced by extracellular histones. In conclusion, we show that GSPE has a protective effect on lymphocyte apoptosis induced by extracellular histones. This study suggests GSPE as a potential therapeutic agent that could help reduce lymphocyte apoptosis, and thus the state of immunosuppression was observed in septic patients. PeerJ Inc. 2017-03-21 /pmc/articles/PMC5363264/ /pubmed/28344907 http://dx.doi.org/10.7717/peerj.3108 Text en © 2017 Chang et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Cell Biology
Chang, Ping
Mo, Bing
Cauvi, David M.
Yu, Ying
Guo, Zhenhui
Zhou, Jian
Huang, Qiong
Yan, Qitao
Chen, Guiming
Liu, Zhanguo
Grape seed proanthocyanidin extract protects lymphocytes against histone-induced apoptosis
title Grape seed proanthocyanidin extract protects lymphocytes against histone-induced apoptosis
title_full Grape seed proanthocyanidin extract protects lymphocytes against histone-induced apoptosis
title_fullStr Grape seed proanthocyanidin extract protects lymphocytes against histone-induced apoptosis
title_full_unstemmed Grape seed proanthocyanidin extract protects lymphocytes against histone-induced apoptosis
title_short Grape seed proanthocyanidin extract protects lymphocytes against histone-induced apoptosis
title_sort grape seed proanthocyanidin extract protects lymphocytes against histone-induced apoptosis
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363264/
https://www.ncbi.nlm.nih.gov/pubmed/28344907
http://dx.doi.org/10.7717/peerj.3108
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