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Cubic Membranes Formation in Synchronized Human Hepatocellular Carcinoma Cells Reveals a Possible Role as a Structural Antioxidant Defense System in Cell Cycle Progression

Cubic membranes (CMs) represent unique biological membrane structures with highly curved three-dimensional periodic minimal surfaces, which have been observed in a wide range of cell types and organelles under various stress conditions (e. g., starvation, virus-infection, and oxidation). However, th...

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Autores principales: Kong, Deqin, Liu, Rui, Liu, Jiangzheng, Zhou, Qingbiao, Zhang, Jiaxin, Li, Wenli, Bai, Hua, Hai, Chunxu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769198/
https://www.ncbi.nlm.nih.gov/pubmed/33381509
http://dx.doi.org/10.3389/fcell.2020.617406
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author Kong, Deqin
Liu, Rui
Liu, Jiangzheng
Zhou, Qingbiao
Zhang, Jiaxin
Li, Wenli
Bai, Hua
Hai, Chunxu
author_facet Kong, Deqin
Liu, Rui
Liu, Jiangzheng
Zhou, Qingbiao
Zhang, Jiaxin
Li, Wenli
Bai, Hua
Hai, Chunxu
author_sort Kong, Deqin
collection PubMed
description Cubic membranes (CMs) represent unique biological membrane structures with highly curved three-dimensional periodic minimal surfaces, which have been observed in a wide range of cell types and organelles under various stress conditions (e. g., starvation, virus-infection, and oxidation). However, there are few reports on the biological roles of CMs, especially their roles in cell cycle. Hence, we established a stable cell population of human hepatocellular carcinoma cells (HepG2) of 100% S phase by thymidine treatment, and determined certain parameters in G2 phase released from S phase. Then we found a close relationship between CMs formation and cell cycle, and an increase in reactive oxygen species (ROS) and mitochondrial function. After the synchronization of HepG2 cells were induced, CMs were observed through transmission electron microscope in G2 phase but not in G1, S and M phase. Moreover, the increased ATP production, mitochondrial and intracellular ROS levels were also present in G2 phase, which demonstrated a positive correlation with CMs formation by Pearson correlation analysis. This study suggests that CMs may act as an antioxidant structure in response to mitochondria-derived ROS during G2 phase and thus participate in cell cycle progression.
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spelling pubmed-77691982020-12-29 Cubic Membranes Formation in Synchronized Human Hepatocellular Carcinoma Cells Reveals a Possible Role as a Structural Antioxidant Defense System in Cell Cycle Progression Kong, Deqin Liu, Rui Liu, Jiangzheng Zhou, Qingbiao Zhang, Jiaxin Li, Wenli Bai, Hua Hai, Chunxu Front Cell Dev Biol Cell and Developmental Biology Cubic membranes (CMs) represent unique biological membrane structures with highly curved three-dimensional periodic minimal surfaces, which have been observed in a wide range of cell types and organelles under various stress conditions (e. g., starvation, virus-infection, and oxidation). However, there are few reports on the biological roles of CMs, especially their roles in cell cycle. Hence, we established a stable cell population of human hepatocellular carcinoma cells (HepG2) of 100% S phase by thymidine treatment, and determined certain parameters in G2 phase released from S phase. Then we found a close relationship between CMs formation and cell cycle, and an increase in reactive oxygen species (ROS) and mitochondrial function. After the synchronization of HepG2 cells were induced, CMs were observed through transmission electron microscope in G2 phase but not in G1, S and M phase. Moreover, the increased ATP production, mitochondrial and intracellular ROS levels were also present in G2 phase, which demonstrated a positive correlation with CMs formation by Pearson correlation analysis. This study suggests that CMs may act as an antioxidant structure in response to mitochondria-derived ROS during G2 phase and thus participate in cell cycle progression. Frontiers Media S.A. 2020-12-14 /pmc/articles/PMC7769198/ /pubmed/33381509 http://dx.doi.org/10.3389/fcell.2020.617406 Text en Copyright © 2020 Kong, Liu, Liu, Zhou, Zhang, Li, Bai and Hai. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Kong, Deqin
Liu, Rui
Liu, Jiangzheng
Zhou, Qingbiao
Zhang, Jiaxin
Li, Wenli
Bai, Hua
Hai, Chunxu
Cubic Membranes Formation in Synchronized Human Hepatocellular Carcinoma Cells Reveals a Possible Role as a Structural Antioxidant Defense System in Cell Cycle Progression
title Cubic Membranes Formation in Synchronized Human Hepatocellular Carcinoma Cells Reveals a Possible Role as a Structural Antioxidant Defense System in Cell Cycle Progression
title_full Cubic Membranes Formation in Synchronized Human Hepatocellular Carcinoma Cells Reveals a Possible Role as a Structural Antioxidant Defense System in Cell Cycle Progression
title_fullStr Cubic Membranes Formation in Synchronized Human Hepatocellular Carcinoma Cells Reveals a Possible Role as a Structural Antioxidant Defense System in Cell Cycle Progression
title_full_unstemmed Cubic Membranes Formation in Synchronized Human Hepatocellular Carcinoma Cells Reveals a Possible Role as a Structural Antioxidant Defense System in Cell Cycle Progression
title_short Cubic Membranes Formation in Synchronized Human Hepatocellular Carcinoma Cells Reveals a Possible Role as a Structural Antioxidant Defense System in Cell Cycle Progression
title_sort cubic membranes formation in synchronized human hepatocellular carcinoma cells reveals a possible role as a structural antioxidant defense system in cell cycle progression
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769198/
https://www.ncbi.nlm.nih.gov/pubmed/33381509
http://dx.doi.org/10.3389/fcell.2020.617406
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