Real-time imaging reveals a role for macrophage protrusive motility in melanoma invasion.

IF 7.4 1区 生物学 Q1 CELL BIOLOGY
Journal of Cell Biology Pub Date : 2025-02-03 Epub Date: 2024-11-21 DOI:10.1083/jcb.202403096
Gayathri Ramakrishnan, Veronika Miskolci, Miranda Hunter, Morgan A Giese, Daniela Münch, Yiran Hou, Kevin W Eliceiri, Michael R Lasarev, Richard M White, Anna Huttenlocher
{"title":"Real-time imaging reveals a role for macrophage protrusive motility in melanoma invasion.","authors":"Gayathri Ramakrishnan, Veronika Miskolci, Miranda Hunter, Morgan A Giese, Daniela Münch, Yiran Hou, Kevin W Eliceiri, Michael R Lasarev, Richard M White, Anna Huttenlocher","doi":"10.1083/jcb.202403096","DOIUrl":null,"url":null,"abstract":"<p><p>Macrophages are primary cells of the innate immune system that mediate tumor progression. However, the motile behavior of macrophages and interactions with tumor cells are not well understood. Here, we exploit the optical transparency of larval zebrafish and perform real-time imaging of macrophage-melanoma interactions. We found that macrophages are highly motile in the tumor microenvironment. Macrophages extend dynamic projections between tumor cells that precede invasive melanoma migration. Modulating macrophage motility with a dominant inhibitory mutation in Rac2 inhibits recruitment to the tumor and impairs tumor invasion. However, a hyperactivating mutation in Rac2 does not affect macrophage recruitment but limits macrophage projections into the melanoma mass and reduces invasive melanoma cell migration. Taken together, these findings reveal a role for Rac2-mediated macrophage protrusive motility in melanoma invasion.</p>","PeriodicalId":15211,"journal":{"name":"Journal of Cell Biology","volume":"224 2","pages":""},"PeriodicalIF":7.4000,"publicationDate":"2025-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cell Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1083/jcb.202403096","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/21 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Macrophages are primary cells of the innate immune system that mediate tumor progression. However, the motile behavior of macrophages and interactions with tumor cells are not well understood. Here, we exploit the optical transparency of larval zebrafish and perform real-time imaging of macrophage-melanoma interactions. We found that macrophages are highly motile in the tumor microenvironment. Macrophages extend dynamic projections between tumor cells that precede invasive melanoma migration. Modulating macrophage motility with a dominant inhibitory mutation in Rac2 inhibits recruitment to the tumor and impairs tumor invasion. However, a hyperactivating mutation in Rac2 does not affect macrophage recruitment but limits macrophage projections into the melanoma mass and reduces invasive melanoma cell migration. Taken together, these findings reveal a role for Rac2-mediated macrophage protrusive motility in melanoma invasion.

实时成像揭示了巨噬细胞在黑色素瘤侵袭中的突出运动作用。
巨噬细胞是先天性免疫系统的初级细胞,可介导肿瘤的发展。然而,人们对巨噬细胞的运动行为以及与肿瘤细胞的相互作用还不甚了解。在这里,我们利用幼体斑马鱼的光学透明性,对巨噬细胞与黑色素瘤的相互作用进行了实时成像。我们发现巨噬细胞在肿瘤微环境中具有高度运动性。巨噬细胞在肿瘤细胞之间延伸出动态投影,这些投影先于黑色素瘤的侵袭性迁移。用 Rac2 的显性抑制突变来调节巨噬细胞的运动性,可以抑制巨噬细胞向肿瘤的募集,并阻碍肿瘤的侵袭。然而,Rac2的过度激活突变不会影响巨噬细胞的募集,但会限制巨噬细胞向黑色素瘤瘤体的投射,并减少黑色素瘤细胞的侵袭性迁移。综上所述,这些发现揭示了 Rac2 介导的巨噬细胞突入运动在黑色素瘤侵袭中的作用。
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
Journal of Cell Biology
Journal of Cell Biology 生物-细胞生物学
CiteScore
12.60
自引率
2.60%
发文量
213
审稿时长
1 months
期刊介绍: The Journal of Cell Biology (JCB) is a comprehensive journal dedicated to publishing original discoveries across all realms of cell biology. We invite papers presenting novel cellular or molecular advancements in various domains of basic cell biology, along with applied cell biology research in diverse systems such as immunology, neurobiology, metabolism, virology, developmental biology, and plant biology. We enthusiastically welcome submissions showcasing significant findings of interest to cell biologists, irrespective of the experimental approach.
×
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