Suppr超能文献

线粒体与冻僵的青蛙。

Mitochondria and the Frozen Frog.

作者信息

Storey Janet M, Wu Shaobo, Storey Kenneth B

机构信息

Department of Biology, Carleton University, Ottawa, ON K1S 5B6, Canada.

Institute of Blood Transfusion, Chinese Academy of Medical Sciences (CAMS) and Peking Union Medical College (PUMC), Chengdu 610052, China.

出版信息

Antioxidants (Basel). 2021 Apr 1;10(4):543. doi: 10.3390/antiox10040543.

Abstract

The wood frog, , is the best-studied of a small group of amphibian species that survive whole body freezing during the winter months. These frogs endure the freezing of 65-70% of their total body water in extracellular ice masses. They have implemented multiple adaptations that manage ice formation, deal with freeze-induced ischemia/reperfusion stress, limit cell volume reduction with the production of small molecule cryoprotectants (glucose, urea) and adjust a wide variety of metabolic pathways for prolonged life in a frozen state. All organs, tissues, cells and intracellular organelles are affected by freeze/thaw and its consequences. This article explores mitochondria in the frozen frog with a focus on both the consequences of freezing (e.g., anoxia/ischemia, cell volume reduction) and mitigating defenses (e.g., antioxidants, chaperone proteins, upregulation of mitochondria-encoded genes, enzyme regulation, etc.) in order to identify adaptive strategies that defend and adapt mitochondria in animals that can be frozen for six months or more every year. A particular focus is placed on freeze-responsive genes in wood frogs that are encoded on the mitochondrial genome including , and RNA. These were strongly up-regulated during whole body freezing (24 h at -2.5 °C) in the liver and brain but showed opposing responses to two component stresses: strong upregulation in response to anoxia but no response to dehydration stress. This indicates that freeze-responsive upregulation of mitochondria-encoded genes is triggered by declining oxygen and likely has an adaptive function in supporting cellular energetics under indeterminate lengths of whole body freezing.

摘要

林蛙是一小群能在冬季全身冻结后存活的两栖动物中研究得最为透彻的物种。这些青蛙能承受其全身65 - 70%的水分在细胞外结成冰块。它们具备多种适应性机制来控制冰的形成、应对冻结引发的缺血/再灌注应激、通过产生小分子冷冻保护剂(葡萄糖、尿素)来限制细胞体积减小,并调整多种代谢途径以在冷冻状态下延长寿命。所有器官、组织、细胞和细胞内细胞器都会受到冻融及其后果的影响。本文探讨冷冻青蛙体内的线粒体,重点关注冷冻的后果(如缺氧/缺血、细胞体积减小)以及减轻损伤的防御机制(如抗氧化剂、伴侣蛋白、线粒体编码基因的上调、酶调节等),以便确定在每年能被冷冻六个月或更长时间的动物中保护和使线粒体适应的适应性策略。特别关注林蛙线粒体基因组上编码的冷冻响应基因,包括 、 和RNA。这些基因在肝脏和大脑全身冷冻(-2.5℃下24小时)期间强烈上调,但对两种组成应激表现出相反的反应:对缺氧有强烈上调反应,但对脱水应激无反应。这表明线粒体编码基因的冷冻响应上调是由氧气减少触发的,并且可能在支持全身冷冻不确定时长下的细胞能量代谢方面具有适应性功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ce5/8067143/0f699896f0b8/antioxidants-10-00543-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验