Loading…
Cancer-associated fibroblasts actively compress cancer cells and modulate mechanotransduction
Abstract During tumor progression, cancer-associated fibroblasts (CAFs) accumulate in tumors and produce an excessive extracellular matrix (ECM), forming a capsule that enwraps cancer cells. This capsule acts as a barrier that restricts tumor growth leading to the buildup of intratumoral pressure. C...
Saved in:
Published in: | Nature communications 2023-11, Vol.14 (1) |
---|---|
Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | |
container_issue | 1 |
container_start_page | |
container_title | Nature communications |
container_volume | 14 |
creator | Barbazan, Jorge Pérez-González, Carlos Gómez-González, Manuel Dedenon, Mathieu Richon, Sophie Latorre, Ernest Serra, Marco Mariani, Pascale Descroix, Stéphanie Sens, Pierre Trepat, Xavier Vignjevic, Danijela Matic |
description | Abstract During tumor progression, cancer-associated fibroblasts (CAFs) accumulate in tumors and produce an excessive extracellular matrix (ECM), forming a capsule that enwraps cancer cells. This capsule acts as a barrier that restricts tumor growth leading to the buildup of intratumoral pressure. Combining genetic and physical manipulations in vivo with microfabrication and force measurements in vitro, we found that the CAFs capsule is not a passive barrier but instead actively compresses cancer cells using actomyosin contractility. Abrogation of CAFs contractility in vivo leads to the dissipation of compressive forces and impairment of capsule formation. By mapping CAF force patterns in 3D, we show that compression is a CAF-intrinsic property independent of cancer cell growth. Supracellular coordination of CAFs is achieved through fibronectin cables that serve as scaffolds allowing force transmission. Cancer cells mechanosense CAF compression, resulting in an altered localization of the transcriptional regulator YAP and a decrease in proliferation. Our study unveils that the contractile capsule actively compresses cancer cells, modulates their mechanical signaling, and reorganizes tumor morphology. |
doi_str_mv | 10.1038/s41467-023-42382-4 |
format | article |
fullrecord | <record><control><sourceid>hal</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_04787318v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>oai_HAL_hal_04787318v1</sourcerecordid><originalsourceid>FETCH-hal_primary_oai_HAL_hal_04787318v13</originalsourceid><addsrcrecordid>eNqVi00PATEYhBshIfgDTr06lH7F1lGEODi6yubVrah0W-m7JP69JQ6u5jKTmWcImQg-E1yZOWqhFwXjUjEtlZFMd8hAci2YKKTq_uQ-GSNeeSu1FEbrATmuIVqXGSAm66FxFT37U06nANggBdv4hwtPalN9yw6R2g9PrQuhnWNF61TdQ3uktbMXiKnJELG6t8cUR6R3hoBu_PUhmW43h_WOXSCUt-xryM8ygS93q3357rguTKGEeQj1D_sCJtRQVw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Cancer-associated fibroblasts actively compress cancer cells and modulate mechanotransduction</title><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><source>Nature</source><source>PubMed Central</source><source>Springer Nature - nature.com Journals - Fully Open Access</source><creator>Barbazan, Jorge ; Pérez-González, Carlos ; Gómez-González, Manuel ; Dedenon, Mathieu ; Richon, Sophie ; Latorre, Ernest ; Serra, Marco ; Mariani, Pascale ; Descroix, Stéphanie ; Sens, Pierre ; Trepat, Xavier ; Vignjevic, Danijela Matic</creator><creatorcontrib>Barbazan, Jorge ; Pérez-González, Carlos ; Gómez-González, Manuel ; Dedenon, Mathieu ; Richon, Sophie ; Latorre, Ernest ; Serra, Marco ; Mariani, Pascale ; Descroix, Stéphanie ; Sens, Pierre ; Trepat, Xavier ; Vignjevic, Danijela Matic</creatorcontrib><description>Abstract During tumor progression, cancer-associated fibroblasts (CAFs) accumulate in tumors and produce an excessive extracellular matrix (ECM), forming a capsule that enwraps cancer cells. This capsule acts as a barrier that restricts tumor growth leading to the buildup of intratumoral pressure. Combining genetic and physical manipulations in vivo with microfabrication and force measurements in vitro, we found that the CAFs capsule is not a passive barrier but instead actively compresses cancer cells using actomyosin contractility. Abrogation of CAFs contractility in vivo leads to the dissipation of compressive forces and impairment of capsule formation. By mapping CAF force patterns in 3D, we show that compression is a CAF-intrinsic property independent of cancer cell growth. Supracellular coordination of CAFs is achieved through fibronectin cables that serve as scaffolds allowing force transmission. Cancer cells mechanosense CAF compression, resulting in an altered localization of the transcriptional regulator YAP and a decrease in proliferation. Our study unveils that the contractile capsule actively compresses cancer cells, modulates their mechanical signaling, and reorganizes tumor morphology.</description><identifier>ISSN: 2041-1723</identifier><identifier>EISSN: 2041-1723</identifier><identifier>DOI: 10.1038/s41467-023-42382-4</identifier><language>eng</language><publisher>Nature Publishing Group</publisher><subject>Life Sciences</subject><ispartof>Nature communications, 2023-11, Vol.14 (1)</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-5091-0411 ; 0000-0003-0027-352X ; 0000-0002-7621-5214 ; 0000-0003-4250-703X ; 0000-0002-7165-8497 ; 0000-0003-4523-3791 ; 0000-0002-7621-5214 ; 0000-0002-7165-8497 ; 0000-0002-5091-0411 ; 0000-0003-0027-352X ; 0000-0003-4523-3791 ; 0000-0003-4250-703X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://hal.science/hal-04787318$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Barbazan, Jorge</creatorcontrib><creatorcontrib>Pérez-González, Carlos</creatorcontrib><creatorcontrib>Gómez-González, Manuel</creatorcontrib><creatorcontrib>Dedenon, Mathieu</creatorcontrib><creatorcontrib>Richon, Sophie</creatorcontrib><creatorcontrib>Latorre, Ernest</creatorcontrib><creatorcontrib>Serra, Marco</creatorcontrib><creatorcontrib>Mariani, Pascale</creatorcontrib><creatorcontrib>Descroix, Stéphanie</creatorcontrib><creatorcontrib>Sens, Pierre</creatorcontrib><creatorcontrib>Trepat, Xavier</creatorcontrib><creatorcontrib>Vignjevic, Danijela Matic</creatorcontrib><title>Cancer-associated fibroblasts actively compress cancer cells and modulate mechanotransduction</title><title>Nature communications</title><description>Abstract During tumor progression, cancer-associated fibroblasts (CAFs) accumulate in tumors and produce an excessive extracellular matrix (ECM), forming a capsule that enwraps cancer cells. This capsule acts as a barrier that restricts tumor growth leading to the buildup of intratumoral pressure. Combining genetic and physical manipulations in vivo with microfabrication and force measurements in vitro, we found that the CAFs capsule is not a passive barrier but instead actively compresses cancer cells using actomyosin contractility. Abrogation of CAFs contractility in vivo leads to the dissipation of compressive forces and impairment of capsule formation. By mapping CAF force patterns in 3D, we show that compression is a CAF-intrinsic property independent of cancer cell growth. Supracellular coordination of CAFs is achieved through fibronectin cables that serve as scaffolds allowing force transmission. Cancer cells mechanosense CAF compression, resulting in an altered localization of the transcriptional regulator YAP and a decrease in proliferation. Our study unveils that the contractile capsule actively compresses cancer cells, modulates their mechanical signaling, and reorganizes tumor morphology.</description><subject>Life Sciences</subject><issn>2041-1723</issn><issn>2041-1723</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqVi00PATEYhBshIfgDTr06lH7F1lGEODi6yubVrah0W-m7JP69JQ6u5jKTmWcImQg-E1yZOWqhFwXjUjEtlZFMd8hAci2YKKTq_uQ-GSNeeSu1FEbrATmuIVqXGSAm66FxFT37U06nANggBdv4hwtPalN9yw6R2g9PrQuhnWNF61TdQ3uktbMXiKnJELG6t8cUR6R3hoBu_PUhmW43h_WOXSCUt-xryM8ygS93q3357rguTKGEeQj1D_sCJtRQVw</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Barbazan, Jorge</creator><creator>Pérez-González, Carlos</creator><creator>Gómez-González, Manuel</creator><creator>Dedenon, Mathieu</creator><creator>Richon, Sophie</creator><creator>Latorre, Ernest</creator><creator>Serra, Marco</creator><creator>Mariani, Pascale</creator><creator>Descroix, Stéphanie</creator><creator>Sens, Pierre</creator><creator>Trepat, Xavier</creator><creator>Vignjevic, Danijela Matic</creator><general>Nature Publishing Group</general><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-5091-0411</orcidid><orcidid>https://orcid.org/0000-0003-0027-352X</orcidid><orcidid>https://orcid.org/0000-0002-7621-5214</orcidid><orcidid>https://orcid.org/0000-0003-4250-703X</orcidid><orcidid>https://orcid.org/0000-0002-7165-8497</orcidid><orcidid>https://orcid.org/0000-0003-4523-3791</orcidid><orcidid>https://orcid.org/0000-0002-7621-5214</orcidid><orcidid>https://orcid.org/0000-0002-7165-8497</orcidid><orcidid>https://orcid.org/0000-0002-5091-0411</orcidid><orcidid>https://orcid.org/0000-0003-0027-352X</orcidid><orcidid>https://orcid.org/0000-0003-4523-3791</orcidid><orcidid>https://orcid.org/0000-0003-4250-703X</orcidid></search><sort><creationdate>20231101</creationdate><title>Cancer-associated fibroblasts actively compress cancer cells and modulate mechanotransduction</title><author>Barbazan, Jorge ; Pérez-González, Carlos ; Gómez-González, Manuel ; Dedenon, Mathieu ; Richon, Sophie ; Latorre, Ernest ; Serra, Marco ; Mariani, Pascale ; Descroix, Stéphanie ; Sens, Pierre ; Trepat, Xavier ; Vignjevic, Danijela Matic</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-hal_primary_oai_HAL_hal_04787318v13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Life Sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barbazan, Jorge</creatorcontrib><creatorcontrib>Pérez-González, Carlos</creatorcontrib><creatorcontrib>Gómez-González, Manuel</creatorcontrib><creatorcontrib>Dedenon, Mathieu</creatorcontrib><creatorcontrib>Richon, Sophie</creatorcontrib><creatorcontrib>Latorre, Ernest</creatorcontrib><creatorcontrib>Serra, Marco</creatorcontrib><creatorcontrib>Mariani, Pascale</creatorcontrib><creatorcontrib>Descroix, Stéphanie</creatorcontrib><creatorcontrib>Sens, Pierre</creatorcontrib><creatorcontrib>Trepat, Xavier</creatorcontrib><creatorcontrib>Vignjevic, Danijela Matic</creatorcontrib><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Nature communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barbazan, Jorge</au><au>Pérez-González, Carlos</au><au>Gómez-González, Manuel</au><au>Dedenon, Mathieu</au><au>Richon, Sophie</au><au>Latorre, Ernest</au><au>Serra, Marco</au><au>Mariani, Pascale</au><au>Descroix, Stéphanie</au><au>Sens, Pierre</au><au>Trepat, Xavier</au><au>Vignjevic, Danijela Matic</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cancer-associated fibroblasts actively compress cancer cells and modulate mechanotransduction</atitle><jtitle>Nature communications</jtitle><date>2023-11-01</date><risdate>2023</risdate><volume>14</volume><issue>1</issue><issn>2041-1723</issn><eissn>2041-1723</eissn><abstract>Abstract During tumor progression, cancer-associated fibroblasts (CAFs) accumulate in tumors and produce an excessive extracellular matrix (ECM), forming a capsule that enwraps cancer cells. This capsule acts as a barrier that restricts tumor growth leading to the buildup of intratumoral pressure. Combining genetic and physical manipulations in vivo with microfabrication and force measurements in vitro, we found that the CAFs capsule is not a passive barrier but instead actively compresses cancer cells using actomyosin contractility. Abrogation of CAFs contractility in vivo leads to the dissipation of compressive forces and impairment of capsule formation. By mapping CAF force patterns in 3D, we show that compression is a CAF-intrinsic property independent of cancer cell growth. Supracellular coordination of CAFs is achieved through fibronectin cables that serve as scaffolds allowing force transmission. Cancer cells mechanosense CAF compression, resulting in an altered localization of the transcriptional regulator YAP and a decrease in proliferation. Our study unveils that the contractile capsule actively compresses cancer cells, modulates their mechanical signaling, and reorganizes tumor morphology.</abstract><pub>Nature Publishing Group</pub><doi>10.1038/s41467-023-42382-4</doi><orcidid>https://orcid.org/0000-0002-5091-0411</orcidid><orcidid>https://orcid.org/0000-0003-0027-352X</orcidid><orcidid>https://orcid.org/0000-0002-7621-5214</orcidid><orcidid>https://orcid.org/0000-0003-4250-703X</orcidid><orcidid>https://orcid.org/0000-0002-7165-8497</orcidid><orcidid>https://orcid.org/0000-0003-4523-3791</orcidid><orcidid>https://orcid.org/0000-0002-7621-5214</orcidid><orcidid>https://orcid.org/0000-0002-7165-8497</orcidid><orcidid>https://orcid.org/0000-0002-5091-0411</orcidid><orcidid>https://orcid.org/0000-0003-0027-352X</orcidid><orcidid>https://orcid.org/0000-0003-4523-3791</orcidid><orcidid>https://orcid.org/0000-0003-4250-703X</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2041-1723 |
ispartof | Nature communications, 2023-11, Vol.14 (1) |
issn | 2041-1723 2041-1723 |
language | eng |
recordid | cdi_hal_primary_oai_HAL_hal_04787318v1 |
source | Publicly Available Content Database (Proquest) (PQ_SDU_P3); Nature; PubMed Central; Springer Nature - nature.com Journals - Fully Open Access |
subjects | Life Sciences |
title | Cancer-associated fibroblasts actively compress cancer cells and modulate mechanotransduction |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T12%3A38%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-hal&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cancer-associated%20fibroblasts%20actively%20compress%20cancer%20cells%20and%20modulate%20mechanotransduction&rft.jtitle=Nature%20communications&rft.au=Barbazan,%20Jorge&rft.date=2023-11-01&rft.volume=14&rft.issue=1&rft.issn=2041-1723&rft.eissn=2041-1723&rft_id=info:doi/10.1038/s41467-023-42382-4&rft_dat=%3Chal%3Eoai_HAL_hal_04787318v1%3C/hal%3E%3Cgrp_id%3Ecdi_FETCH-hal_primary_oai_HAL_hal_04787318v13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |