Experimentally induced metamorphosis in axolotls reduces regenerative rate and fidelity.

Regeneration (Oxford, England) Pub Date : 2014-02-20 eCollection Date: 2014-02-01 DOI:10.1002/reg2.8
James R Monaghan, Adrian C Stier, François Michonneau, Matthew D Smith, Bret Pasch, Malcolm Maden, Ashley W Seifert
{"title":"Experimentally induced metamorphosis in axolotls reduces regenerative rate and fidelity.","authors":"James R Monaghan,&nbsp;Adrian C Stier,&nbsp;François Michonneau,&nbsp;Matthew D Smith,&nbsp;Bret Pasch,&nbsp;Malcolm Maden,&nbsp;Ashley W Seifert","doi":"10.1002/reg2.8","DOIUrl":null,"url":null,"abstract":"<p><p>While most tetrapods are unable to regenerate severed body parts, amphibians display a remarkable ability to regenerate an array of structures. Frogs can regenerate appendages as larva, but they lose this ability around metamorphosis. In contrast, salamanders regenerate appendages as larva, juveniles, and adults. However, the extent to which fundamental traits (e.g., metamorphosis, body size, aging, etc.) restrict regenerative ability remains contentious. Here we utilize the ability of normally paedomorphic adult axolotls (Ambystoma mexicanum) to undergo induced metamorphosis by thyroxine exposure to test how metamorphosis and body size affects regeneration in age-matched paedomorphic and metamorphic individuals. We show that body size does not affect regeneration in adult axolotls, but metamorphosis causes a twofold reduction in regeneration rate, and lead to carpal and digit malformations. Furthermore, we find evidence that metamorphic blastemal cells may take longer to traverse the cell cycle and display a lower proliferative rate. This study identifies the axolotl as a powerful system to study how metamorphosis restricts regeneration independently of developmental stage, body size, and age; and more broadly how metamorphosis affects tissue-specific changes.</p>","PeriodicalId":90316,"journal":{"name":"Regeneration (Oxford, England)","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2014-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/reg2.8","citationCount":"69","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Regeneration (Oxford, England)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/reg2.8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2014/2/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 69

Abstract

While most tetrapods are unable to regenerate severed body parts, amphibians display a remarkable ability to regenerate an array of structures. Frogs can regenerate appendages as larva, but they lose this ability around metamorphosis. In contrast, salamanders regenerate appendages as larva, juveniles, and adults. However, the extent to which fundamental traits (e.g., metamorphosis, body size, aging, etc.) restrict regenerative ability remains contentious. Here we utilize the ability of normally paedomorphic adult axolotls (Ambystoma mexicanum) to undergo induced metamorphosis by thyroxine exposure to test how metamorphosis and body size affects regeneration in age-matched paedomorphic and metamorphic individuals. We show that body size does not affect regeneration in adult axolotls, but metamorphosis causes a twofold reduction in regeneration rate, and lead to carpal and digit malformations. Furthermore, we find evidence that metamorphic blastemal cells may take longer to traverse the cell cycle and display a lower proliferative rate. This study identifies the axolotl as a powerful system to study how metamorphosis restricts regeneration independently of developmental stage, body size, and age; and more broadly how metamorphosis affects tissue-specific changes.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
实验诱导的蝾螈变态会降低再生速率和保真度。
虽然大多数四足动物无法再生被切断的身体部位,但两栖动物显示出再生一系列结构的非凡能力。青蛙在幼虫时期可以再生附属物,但在变态时期就失去了这种能力。相比之下,蝾螈在幼虫、幼体和成年时再生附属物。然而,基本特征(如变形、体型、衰老等)在多大程度上限制了再生能力仍然存在争议。在这里,我们利用正常幼态的成年美西螈(Ambystoma mexicanum)暴露在甲状腺素下诱导变态的能力,来测试变态和体型如何影响年龄匹配的幼态和变态个体的再生。我们发现,体型大小不影响成年蝾螈的再生,但变态会导致再生率降低两倍,并导致腕关节和手指畸形。此外,我们发现证据表明,变态胚细胞可能需要更长的时间来穿越细胞周期,并显示出较低的增殖率。本研究确定了美西螈作为一个强大的系统来研究如何蜕变限制再生独立于发育阶段,体型和年龄;更广泛地说,变态是如何影响组织特异性变化的。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Does urban renewal impact social interaction in public open space? Evidence from Sham Shui Po, Hong Kong Regenerating Hong Kong’s New Towns: Resilience and Collaboration in the Context of Polycentric Urban Development Urban Regeneration-Is it possible for the environmental regeneration of Hong Kong to begin from Kau Yi Chau Island? Reimagining Heath Park - A complex systems approach to urban re-generation The Asian City: Regeneration as Value Added
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1