在飞行肌发育过程中成肌细胞增殖不受神经信号减少的影响

IF 1.7 3区 农林科学 Q2 ENTOMOLOGY
J. Clark Ludwig, Barry Trimmer
{"title":"在飞行肌发育过程中成肌细胞增殖不受神经信号减少的影响","authors":"J. Clark Ludwig,&nbsp;Barry Trimmer","doi":"10.1016/j.asd.2022.101232","DOIUrl":null,"url":null,"abstract":"<div><p>In holometabolous insects, metamorphosis involves restructuring the musculature to accommodate adult-specific anatomy and behaviors. Evidence from experiments on remodeled muscles, as well as those that develop <em>de novo</em><span>, suggests that signals from the nervous system<span><span> support adult muscle development by controlling </span>myoblast proliferation rate. However, the dorsolongitudinal flight muscles (DLMs) of </span></span><span><em>Manduca sexta</em></span><span><span> undergo a mixed developmental program involving larval muscle fibers, and it is not known if neurons play the same role in the formation of these muscles. To address this question, we have blocked the most promising candidate pathways for neural input and examined the DLMs for changes in proliferation. Our results show that DLM development does not depend on neural activity, Hedgehog signaling, or </span>EGF signaling. It remains to be determined how DLM growth is controlled and why neurally mediated proliferation differs between individual muscles.</span></p></div>","PeriodicalId":55461,"journal":{"name":"Arthropod Structure & Development","volume":null,"pages":null},"PeriodicalIF":1.7000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Myoblast proliferation during flight muscle development in Manduca sexta is unaffected by reduced neural signaling\",\"authors\":\"J. Clark Ludwig,&nbsp;Barry Trimmer\",\"doi\":\"10.1016/j.asd.2022.101232\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>In holometabolous insects, metamorphosis involves restructuring the musculature to accommodate adult-specific anatomy and behaviors. Evidence from experiments on remodeled muscles, as well as those that develop <em>de novo</em><span>, suggests that signals from the nervous system<span><span> support adult muscle development by controlling </span>myoblast proliferation rate. However, the dorsolongitudinal flight muscles (DLMs) of </span></span><span><em>Manduca sexta</em></span><span><span> undergo a mixed developmental program involving larval muscle fibers, and it is not known if neurons play the same role in the formation of these muscles. To address this question, we have blocked the most promising candidate pathways for neural input and examined the DLMs for changes in proliferation. Our results show that DLM development does not depend on neural activity, Hedgehog signaling, or </span>EGF signaling. It remains to be determined how DLM growth is controlled and why neurally mediated proliferation differs between individual muscles.</span></p></div>\",\"PeriodicalId\":55461,\"journal\":{\"name\":\"Arthropod Structure & Development\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Arthropod Structure & Development\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1467803922000937\",\"RegionNum\":3,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENTOMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Arthropod Structure & Development","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1467803922000937","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

在全变态昆虫中,变态包括重组肌肉组织,以适应成虫特定的解剖结构和行为。来自重塑肌肉和新生肌肉实验的证据表明,来自神经系统的信号通过控制成肌细胞增殖率来支持成年肌肉的发育。然而,六齿Manduca的背纵飞行肌(DLM)经历了一个涉及幼虫肌肉纤维的混合发育程序,目前尚不清楚神经元是否在这些肌肉的形成中发挥着相同的作用。为了解决这个问题,我们阻断了最有希望的神经输入候选途径,并检查了DLM的增殖变化。我们的研究结果表明,DLM的发展不依赖于神经活动、Hedgehog信号或EGF信号。DLM的生长是如何控制的,以及为什么神经介导的增殖在单个肌肉之间不同,还有待确定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Myoblast proliferation during flight muscle development in Manduca sexta is unaffected by reduced neural signaling

In holometabolous insects, metamorphosis involves restructuring the musculature to accommodate adult-specific anatomy and behaviors. Evidence from experiments on remodeled muscles, as well as those that develop de novo, suggests that signals from the nervous system support adult muscle development by controlling myoblast proliferation rate. However, the dorsolongitudinal flight muscles (DLMs) of Manduca sexta undergo a mixed developmental program involving larval muscle fibers, and it is not known if neurons play the same role in the formation of these muscles. To address this question, we have blocked the most promising candidate pathways for neural input and examined the DLMs for changes in proliferation. Our results show that DLM development does not depend on neural activity, Hedgehog signaling, or EGF signaling. It remains to be determined how DLM growth is controlled and why neurally mediated proliferation differs between individual muscles.

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
3.50
自引率
10.00%
发文量
54
审稿时长
60 days
期刊介绍: Arthropod Structure & Development is a Journal of Arthropod Structural Biology, Development, and Functional Morphology; it considers manuscripts that deal with micro- and neuroanatomy, development, biomechanics, organogenesis in particular under comparative and evolutionary aspects but not merely taxonomic papers. The aim of the journal is to publish papers in the areas of functional and comparative anatomy and development, with an emphasis on the role of cellular organization in organ function. The journal will also publish papers on organogenisis, embryonic and postembryonic development, and organ or tissue regeneration and repair. Manuscripts dealing with comparative and evolutionary aspects of microanatomy and development are encouraged.
×
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