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人类红细胞中代谢途径与氧化应激增加之间的相互作用

Interplay Between Metabolic Pathways and Increased Oxidative Stress in Human Red Blood Cells.

作者信息

Spinelli Sara, Marino Angela, Morabito Rossana, Remigante Alessia

机构信息

Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, 98166 Messina, Italy.

出版信息

Cells. 2024 Dec 7;13(23):2026. doi: 10.3390/cells13232026.

DOI:10.3390/cells13232026
PMID:39682773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11640724/
Abstract

Red blood cells (RBCs) are highly specialized cells with a limited metabolic repertoire. However, it has been demonstrated that metabolic processes are affected by the production of reactive oxygen species (ROS), and critical enzymes allied to metabolic pathways can be impaired by redox reactions. Thus, oxidative stress-induced alternations in the metabolic pathways can contribute to cell dysfunction of human RBCs. Herein, we aim to provide an overview on the metabolic pathways of human RBCs, focusing on their pathophysiological relevance and their regulation in oxidative stress-related conditions.

摘要

红细胞(RBCs)是高度特化的细胞,其代谢功能有限。然而,已经证明代谢过程会受到活性氧(ROS)产生的影响,并且与代谢途径相关的关键酶可能会因氧化还原反应而受损。因此,氧化应激诱导的代谢途径改变可能导致人类红细胞的细胞功能障碍。在此,我们旨在概述人类红细胞的代谢途径,重点关注其病理生理相关性以及在氧化应激相关条件下的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/2934410fdf67/cells-13-02026-g013a.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/549c8179216a/cells-13-02026-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/18b14bf9c8df/cells-13-02026-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/0b582a9f0073/cells-13-02026-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/8fffe2128cfb/cells-13-02026-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/44f17fbcd41d/cells-13-02026-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/15ad4f1141e8/cells-13-02026-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/ac2ba92166dc/cells-13-02026-g009.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/bddacdf382bf/cells-13-02026-g011.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/2934410fdf67/cells-13-02026-g013a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/b213f0706168/cells-13-02026-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/549c8179216a/cells-13-02026-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/18b14bf9c8df/cells-13-02026-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/ce9d6630919c/cells-13-02026-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/0b582a9f0073/cells-13-02026-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/8fffe2128cfb/cells-13-02026-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/44f17fbcd41d/cells-13-02026-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/15ad4f1141e8/cells-13-02026-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/ac2ba92166dc/cells-13-02026-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/0045385ef270/cells-13-02026-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/bddacdf382bf/cells-13-02026-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/27d64706118f/cells-13-02026-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fe/11640724/2934410fdf67/cells-13-02026-g013a.jpg

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2
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3
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Med Oncol. 2025 Aug 2;42(9):399. doi: 10.1007/s12032-025-02940-w.
4
Erythrocytes enhance oxygen-carrying capacity through self-regulation.红细胞通过自我调节增强携氧能力。
Front Physiol. 2025 May 16;16:1592176. doi: 10.3389/fphys.2025.1592176. eCollection 2025.
5
Deciphering Oxidative Stress in Cardiovascular Disease Progression: A Blueprint for Mechanistic Understanding and Therapeutic Innovation.解读心血管疾病进展中的氧化应激:机制理解与治疗创新蓝图
Antioxidants (Basel). 2024 Dec 31;14(1):38. doi: 10.3390/antiox14010038.
Front Physiol. 2023 Dec 4;14:1303815. doi: 10.3389/fphys.2023.1303815. eCollection 2023.
4
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5
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Transfus Med Rev. 2023 Jul;37(3):150748. doi: 10.1016/j.tmrv.2023.150748. Epub 2023 Jul 13.
6
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7
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