作为天体生物学研究模型的盐水虾:对类似火星的大气压力条件的生理适应。

IF 2.1 3区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Maria Teresa Muscari Tomajoli , Paola Di Donato , Vincenzo Della Corte , Giovanni Covone , Gianluca Fasciolo , Eugenio Geremia , Adriana Petito , Luca Tonietti , Laura Inno , Alessandra Rotundi , Paola Venditti , Gaetana Napolitano
{"title":"作为天体生物学研究模型的盐水虾:对类似火星的大气压力条件的生理适应。","authors":"Maria Teresa Muscari Tomajoli ,&nbsp;Paola Di Donato ,&nbsp;Vincenzo Della Corte ,&nbsp;Giovanni Covone ,&nbsp;Gianluca Fasciolo ,&nbsp;Eugenio Geremia ,&nbsp;Adriana Petito ,&nbsp;Luca Tonietti ,&nbsp;Laura Inno ,&nbsp;Alessandra Rotundi ,&nbsp;Paola Venditti ,&nbsp;Gaetana Napolitano","doi":"10.1016/j.cbpa.2025.111825","DOIUrl":null,"url":null,"abstract":"<div><div>Understanding the adaptation mechanisms of extremophiles to extreme environments is fundamental to predicting organisms' capacity to survive in space and plan future space exploration missions. This study explores the physiological and metabolic adaptations of nauplii of a eukaryotic organism, <em>Artemia franciscana</em>, hatched from cysts exposed to Mars-like pressure conditions (6 mbar) by analyzing aerobic and anaerobic metabolism, mitochondrial function, and oxidative stress in nauplii. Mars-like pressure did not inhibit nauplii's hatching or <em>in vivo</em> respiration, indicating that the fundamental metabolic functions are preserved but affected cellular metabolism. The lower lactate levels suggested reduced anaerobic metabolism, and the reduction in the activity of Complex I of the electron transport chain, resulting in reduced <em>in vitro</em> respiration supported by pyruvate plus malate, suggested an effect on aerobic metabolism. However, the succinate-supported respiration remained stable according to unchanged Complex II activity. Changes in aerobic metabolism could affect Reactive Oxygen Species (ROS) production and management. We did not observe changes in ROS levels according to the unchanged activity of NADPH oxidase, a source of ROS in the early development stages of nauplii. A total antioxidant capacity reduction and increased susceptibility to oxidants were observed despite this. However, lipid and protein oxidative stress markers levels remained unchanged, likely due to the increased activity of antioxidant enzymes. Our results underscore the resilience of the cysts to Mars-like pressure conditions, indicating the potential of <em>Artemia franciscana</em> as a model organism in astrobiological research, opening new avenues for exploration in astrobiology.</div></div>","PeriodicalId":55237,"journal":{"name":"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology","volume":"303 ","pages":"Article 111825"},"PeriodicalIF":2.1000,"publicationDate":"2025-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The brine shrimp Artemia franciscana as a model for astrobiological studies: Physiological adaptations to Mars-like atmospheric pressure conditions\",\"authors\":\"Maria Teresa Muscari Tomajoli ,&nbsp;Paola Di Donato ,&nbsp;Vincenzo Della Corte ,&nbsp;Giovanni Covone ,&nbsp;Gianluca Fasciolo ,&nbsp;Eugenio Geremia ,&nbsp;Adriana Petito ,&nbsp;Luca Tonietti ,&nbsp;Laura Inno ,&nbsp;Alessandra Rotundi ,&nbsp;Paola Venditti ,&nbsp;Gaetana Napolitano\",\"doi\":\"10.1016/j.cbpa.2025.111825\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Understanding the adaptation mechanisms of extremophiles to extreme environments is fundamental to predicting organisms' capacity to survive in space and plan future space exploration missions. This study explores the physiological and metabolic adaptations of nauplii of a eukaryotic organism, <em>Artemia franciscana</em>, hatched from cysts exposed to Mars-like pressure conditions (6 mbar) by analyzing aerobic and anaerobic metabolism, mitochondrial function, and oxidative stress in nauplii. Mars-like pressure did not inhibit nauplii's hatching or <em>in vivo</em> respiration, indicating that the fundamental metabolic functions are preserved but affected cellular metabolism. The lower lactate levels suggested reduced anaerobic metabolism, and the reduction in the activity of Complex I of the electron transport chain, resulting in reduced <em>in vitro</em> respiration supported by pyruvate plus malate, suggested an effect on aerobic metabolism. However, the succinate-supported respiration remained stable according to unchanged Complex II activity. Changes in aerobic metabolism could affect Reactive Oxygen Species (ROS) production and management. We did not observe changes in ROS levels according to the unchanged activity of NADPH oxidase, a source of ROS in the early development stages of nauplii. A total antioxidant capacity reduction and increased susceptibility to oxidants were observed despite this. However, lipid and protein oxidative stress markers levels remained unchanged, likely due to the increased activity of antioxidant enzymes. Our results underscore the resilience of the cysts to Mars-like pressure conditions, indicating the potential of <em>Artemia franciscana</em> as a model organism in astrobiological research, opening new avenues for exploration in astrobiology.</div></div>\",\"PeriodicalId\":55237,\"journal\":{\"name\":\"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology\",\"volume\":\"303 \",\"pages\":\"Article 111825\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-02-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1095643325000236\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1095643325000236","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

了解极端微生物对极端环境的适应机制对于预测生物在太空中的生存能力和规划未来的太空探索任务至关重要。本研究通过分析nauplii的有氧和无氧代谢、线粒体功能和氧化应激,探讨了一种真核生物Artemia franciscana在暴露于类似火星压力条件(6 mbar)的囊肿中孵化出来的nauplii的生理和代谢适应。火星样的压力并没有抑制nauplii的孵化和体内呼吸,表明基本的代谢功能得到了保留,但影响了细胞代谢。较低的乳酸水平表明无氧代谢减少,电子传递链复合体I活性降低,导致丙酮酸加苹果酸支持的体外呼吸减少,表明对有氧代谢有影响。然而,琥珀酸支持呼吸保持稳定,根据不变的配合物II活性。有氧代谢的变化会影响活性氧(Reactive Oxygen Species, ROS)的产生和管理。根据NADPH氧化酶的活性不变,我们没有观察到ROS水平的变化,NADPH氧化酶是nauplii早期发育阶段ROS的来源。尽管如此,总抗氧化能力降低,对氧化剂的敏感性增加。然而,脂质和蛋白质氧化应激标志物水平保持不变,可能是由于抗氧化酶的活性增加。我们的研究结果强调了Artemia franciscana囊在类似火星的压力条件下的恢复能力,表明了Artemia franciscana作为天体生物学研究的模式生物的潜力,为天体生物学的探索开辟了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The brine shrimp Artemia franciscana as a model for astrobiological studies: Physiological adaptations to Mars-like atmospheric pressure conditions

The brine shrimp Artemia franciscana as a model for astrobiological studies: Physiological adaptations to Mars-like atmospheric pressure conditions
Understanding the adaptation mechanisms of extremophiles to extreme environments is fundamental to predicting organisms' capacity to survive in space and plan future space exploration missions. This study explores the physiological and metabolic adaptations of nauplii of a eukaryotic organism, Artemia franciscana, hatched from cysts exposed to Mars-like pressure conditions (6 mbar) by analyzing aerobic and anaerobic metabolism, mitochondrial function, and oxidative stress in nauplii. Mars-like pressure did not inhibit nauplii's hatching or in vivo respiration, indicating that the fundamental metabolic functions are preserved but affected cellular metabolism. The lower lactate levels suggested reduced anaerobic metabolism, and the reduction in the activity of Complex I of the electron transport chain, resulting in reduced in vitro respiration supported by pyruvate plus malate, suggested an effect on aerobic metabolism. However, the succinate-supported respiration remained stable according to unchanged Complex II activity. Changes in aerobic metabolism could affect Reactive Oxygen Species (ROS) production and management. We did not observe changes in ROS levels according to the unchanged activity of NADPH oxidase, a source of ROS in the early development stages of nauplii. A total antioxidant capacity reduction and increased susceptibility to oxidants were observed despite this. However, lipid and protein oxidative stress markers levels remained unchanged, likely due to the increased activity of antioxidant enzymes. Our results underscore the resilience of the cysts to Mars-like pressure conditions, indicating the potential of Artemia franciscana as a model organism in astrobiological research, opening new avenues for exploration in astrobiology.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
5.00
自引率
4.30%
发文量
155
审稿时长
3 months
期刊介绍: Part A: Molecular & Integrative Physiology of Comparative Biochemistry and Physiology. This journal covers molecular, cellular, integrative, and ecological physiology. Topics include bioenergetics, circulation, development, excretion, ion regulation, endocrinology, neurobiology, nutrition, respiration, and thermal biology. Study on regulatory mechanisms at any level of organization such as signal transduction and cellular interaction and control of behavior are also published.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信