Evolutionary Pressures Behind the Translocation of Hematopoiesis to the Bone Marrow Cavity in Terrestrial Vertebrates.

IF 1.2 4区 医学 Q4 ENVIRONMENTAL SCIENCES
Health physics Pub Date : 2026-09-01 Epub Date: 2026-02-02 DOI:10.1097/HP.0000000000002086
P Andrew Karam, Robert P Gale, James S Welsh
{"title":"Evolutionary Pressures Behind the Translocation of Hematopoiesis to the Bone Marrow Cavity in Terrestrial Vertebrates.","authors":"P Andrew Karam, Robert P Gale, James S Welsh","doi":"10.1097/HP.0000000000002086","DOIUrl":null,"url":null,"abstract":"<p><p>Nearly 400 million years ago, vertebrate life began to transition from a purely aquatic existence to the terrestrial environment. Concurrently, exposure to ionizing radiation from cosmic and geologic sources increased substantially. Around the same time, vertebrate hematopoietic stem cells (HSCs) migrated from the liver and peri-nephric parts of the abdomen into the interior of bones. Interestingly, among today's vertebrates, only fish lack bone marrow. All other extant vertebrates maintain their HSCs in the bone marrow cavity. We propose protection from sub-lethal DNA damage to these long-lived radiation-sensitive cells because of exposure to ionizing radiation is why HSCs are sequestered with the bone marrow cavity. Our calculations support this hypothesis. Residence in the bone marrow cavity reduced exposure to penetrating background radiation and the concomitant DNA damage by at least 20%. This reduction was even more significant radio-biologically when considering the relatively hypoxic conditions within the bone marrow cavity and oxygen's role in enhancing radiogenic DNA damage. This may be particularly relevant considering the oxygen-rich atmosphere in existence at the time of transitioning to a terrestrial habitat. Given the exquisite sensitivity of HSCs and proliferating blood cells to radiation, we propose this translocation provided a selective advantage and that protection from sub-lethal radiogenic DNA damage at least partially explains translocation of hematopoietic cells to the bone marrow cavity in terrestrial vertebrates.</p>","PeriodicalId":12976,"journal":{"name":"Health physics","volume":" ","pages":"179-186"},"PeriodicalIF":1.2000,"publicationDate":"2026-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Health physics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/HP.0000000000002086","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/2/2 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Nearly 400 million years ago, vertebrate life began to transition from a purely aquatic existence to the terrestrial environment. Concurrently, exposure to ionizing radiation from cosmic and geologic sources increased substantially. Around the same time, vertebrate hematopoietic stem cells (HSCs) migrated from the liver and peri-nephric parts of the abdomen into the interior of bones. Interestingly, among today's vertebrates, only fish lack bone marrow. All other extant vertebrates maintain their HSCs in the bone marrow cavity. We propose protection from sub-lethal DNA damage to these long-lived radiation-sensitive cells because of exposure to ionizing radiation is why HSCs are sequestered with the bone marrow cavity. Our calculations support this hypothesis. Residence in the bone marrow cavity reduced exposure to penetrating background radiation and the concomitant DNA damage by at least 20%. This reduction was even more significant radio-biologically when considering the relatively hypoxic conditions within the bone marrow cavity and oxygen's role in enhancing radiogenic DNA damage. This may be particularly relevant considering the oxygen-rich atmosphere in existence at the time of transitioning to a terrestrial habitat. Given the exquisite sensitivity of HSCs and proliferating blood cells to radiation, we propose this translocation provided a selective advantage and that protection from sub-lethal radiogenic DNA damage at least partially explains translocation of hematopoietic cells to the bone marrow cavity in terrestrial vertebrates.

陆生脊椎动物骨髓腔造血易位背后的进化压力。
近4亿年前,脊椎动物开始从纯粹的水生生物过渡到陆地环境。与此同时,来自宇宙和地质源的电离辐射暴露也大大增加。大约在同一时间,脊椎动物造血干细胞(hsc)从肝脏和腹部肾周部分迁移到骨骼内部。有趣的是,在今天的脊椎动物中,只有鱼缺乏骨髓。所有现存的其他脊椎动物都在骨髓腔中维持造血干细胞。我们提出保护这些长寿命的辐射敏感细胞免受亚致死DNA损伤,因为暴露于电离辐射是造血干细胞与骨髓腔隔离的原因。我们的计算支持这一假设。居住在骨髓腔中可减少暴露于穿透性背景辐射和伴随的DNA损伤至少20%。当考虑到骨髓腔内相对缺氧的条件和氧在增强放射性基因DNA损伤中的作用时,这种减少在放射生物学上更为显著。考虑到在向陆地栖息地过渡时存在的富氧大气,这可能特别相关。考虑到造血干细胞和增殖血细胞对辐射的敏感性,我们认为这种易位提供了一种选择优势,并且至少部分解释了陆生脊椎动物造血细胞易位到骨髓腔的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Health physics
Health physics 医学-公共卫生、环境卫生与职业卫生
CiteScore
4.20
自引率
0.00%
发文量
324
审稿时长
3-8 weeks
期刊介绍: Health Physics, first published in 1958, provides the latest research to a wide variety of radiation safety professionals including health physicists, nuclear chemists, medical physicists, and radiation safety officers with interests in nuclear and radiation science. The Journal allows professionals in these and other disciplines in science and engineering to stay on the cutting edge of scientific and technological advances in the field of radiation safety. The Journal publishes original papers, technical notes, articles on advances in practical applications, editorials, and correspondence. Journal articles report on the latest findings in theoretical, practical, and applied disciplines of epidemiology and radiation effects, radiation biology and radiation science, radiation ecology, and related fields.
×
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:604180095
Book学术官方微信
小红书