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Tenascin‐C Activation of Lung Fibroblasts in a 3D Synthetic Lung Extracellular Matrix Mimic
The lung extracellular matrix (ECM) maintains the structural integrity of the tissue and regulates the phenotype and functions of resident fibroblasts. Lung‐metastatic breast cancer alters these cell‐ECM interactions, promoting fibroblast activation. There is a need for bio‐instructive ECM models th...
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Published in: | Advanced materials (Weinheim) 2023-08, Vol.35 (33), p.e2301493-n/a |
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description | The lung extracellular matrix (ECM) maintains the structural integrity of the tissue and regulates the phenotype and functions of resident fibroblasts. Lung‐metastatic breast cancer alters these cell‐ECM interactions, promoting fibroblast activation. There is a need for bio‐instructive ECM models that match the ECM composition and biomechanics of the lung to study these cell‐matrix interactions in vitro. Here, a synthetic, bioactive hydrogel is synthesized that mimics the native lung modulus and includes a representative distribution of the most abundant ECM peptide motifs responsible for integrin‐binding and matrix metalloproteinase (MMP)‐mediated degradation in the lung, which enables quiescent culture of human lung fibroblasts (HLFs). Stimulation with transforming growth factor β1 (TGF‐β1), metastatic breast cancer conditioned media (CM), or tenascin‐C‐derived integrin‐binding peptide activated hydrogel‐encapsulated HLFs demonstrates multiple environmental methods to activate HLFs in a lung ECM‐mimicking hydrogel. This lung hydrogel platform is a tunable, synthetic approach to studying the independent and combinatorial effects of ECM in regulating fibroblast quiescence and activation.
A hydrogel that mimics the protein content and stiffness of healthy lung tissue is synthesized. Lung‐mimicking material is applied to reveal the ability of tenascin‐C to activate fibroblasts in lung‐metastatic breast cancer. This novel hydrogel environment will be incredibly useful for research questions involving the lung extracellular matrix. |
doi_str_mv | 10.1002/adma.202301493 |
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A hydrogel that mimics the protein content and stiffness of healthy lung tissue is synthesized. Lung‐mimicking material is applied to reveal the ability of tenascin‐C to activate fibroblasts in lung‐metastatic breast cancer. This novel hydrogel environment will be incredibly useful for research questions involving the lung extracellular matrix.</description><identifier>ISSN: 0935-9648</identifier><identifier>ISSN: 1521-4095</identifier><identifier>EISSN: 1521-4095</identifier><identifier>DOI: 10.1002/adma.202301493</identifier><identifier>PMID: 37227134</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Binding ; Biomechanics ; Breast cancer ; breast cancer metastasis ; Breast Neoplasms ; Combinatorial analysis ; Extracellular matrix ; Extracellular Matrix - metabolism ; Female ; Fibroblasts ; Growth factors ; Humans ; Hydrogels ; Hydrogels - chemistry ; Integrins - metabolism ; Lung ; Lungs ; Materials science ; Matrix metalloproteinases ; Metastasis ; Peptides ; Peptides - chemistry ; poly(ethylene glycol) ; stiffness ; Structural integrity ; Tenascin - metabolism ; Tenascin - pharmacology</subject><ispartof>Advanced materials (Weinheim), 2023-08, Vol.35 (33), p.e2301493-n/a</ispartof><rights>2023 Wiley‐VCH GmbH</rights><rights>2023 Wiley-VCH GmbH.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4693-96fb1a73beda2369e4787fcdfe87496b510ad5f81375f182a3806272e655bc083</citedby><cites>FETCH-LOGICAL-c4693-96fb1a73beda2369e4787fcdfe87496b510ad5f81375f182a3806272e655bc083</cites><orcidid>0000-0001-8323-6745 ; 0000-0002-5091-3321 ; 0000-0002-7364-8727 ; 0000-0002-2165-771X ; 0000-0001-5200-2153</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37227134$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kundu, Aritra Nath</creatorcontrib><creatorcontrib>Dougan, Carey E.</creatorcontrib><creatorcontrib>Mahmoud, Samar</creatorcontrib><creatorcontrib>Kilic, Alara</creatorcontrib><creatorcontrib>Panagiotou, Alexi</creatorcontrib><creatorcontrib>Richbourg, Nathan R.</creatorcontrib><creatorcontrib>Irakoze, Ninette</creatorcontrib><creatorcontrib>Peyton, Shelly R.</creatorcontrib><title>Tenascin‐C Activation of Lung Fibroblasts in a 3D Synthetic Lung Extracellular Matrix Mimic</title><title>Advanced materials (Weinheim)</title><addtitle>Adv Mater</addtitle><description>The lung extracellular matrix (ECM) maintains the structural integrity of the tissue and regulates the phenotype and functions of resident fibroblasts. Lung‐metastatic breast cancer alters these cell‐ECM interactions, promoting fibroblast activation. There is a need for bio‐instructive ECM models that match the ECM composition and biomechanics of the lung to study these cell‐matrix interactions in vitro. Here, a synthetic, bioactive hydrogel is synthesized that mimics the native lung modulus and includes a representative distribution of the most abundant ECM peptide motifs responsible for integrin‐binding and matrix metalloproteinase (MMP)‐mediated degradation in the lung, which enables quiescent culture of human lung fibroblasts (HLFs). Stimulation with transforming growth factor β1 (TGF‐β1), metastatic breast cancer conditioned media (CM), or tenascin‐C‐derived integrin‐binding peptide activated hydrogel‐encapsulated HLFs demonstrates multiple environmental methods to activate HLFs in a lung ECM‐mimicking hydrogel. This lung hydrogel platform is a tunable, synthetic approach to studying the independent and combinatorial effects of ECM in regulating fibroblast quiescence and activation.
A hydrogel that mimics the protein content and stiffness of healthy lung tissue is synthesized. Lung‐mimicking material is applied to reveal the ability of tenascin‐C to activate fibroblasts in lung‐metastatic breast cancer. This novel hydrogel environment will be incredibly useful for research questions involving the lung extracellular matrix.</description><subject>Binding</subject><subject>Biomechanics</subject><subject>Breast cancer</subject><subject>breast cancer metastasis</subject><subject>Breast Neoplasms</subject><subject>Combinatorial analysis</subject><subject>Extracellular matrix</subject><subject>Extracellular Matrix - metabolism</subject><subject>Female</subject><subject>Fibroblasts</subject><subject>Growth factors</subject><subject>Humans</subject><subject>Hydrogels</subject><subject>Hydrogels - chemistry</subject><subject>Integrins - metabolism</subject><subject>Lung</subject><subject>Lungs</subject><subject>Materials science</subject><subject>Matrix metalloproteinases</subject><subject>Metastasis</subject><subject>Peptides</subject><subject>Peptides - chemistry</subject><subject>poly(ethylene glycol)</subject><subject>stiffness</subject><subject>Structural integrity</subject><subject>Tenascin - metabolism</subject><subject>Tenascin - pharmacology</subject><issn>0935-9648</issn><issn>1521-4095</issn><issn>1521-4095</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFkT1PGzEAhi1UBCnt2rGy1KVLgj_OX1MVBShIiTqUjpXl8_nA6M6m9h0lW38Cv5FfUkeB0Hbp5MGPH7-vXgDeYTTDCJFj0_RmRhChCFeK7oEJZgRPK6TYKzBBirKp4pU8BK9zvkEIKY74ATikghCBaTUB3y9dMNn68PjrYQHndvB3ZvAxwNjC5Riu4JmvU6w7k4cMfYAG0hP4dR2Gazd4u0VO74dkrOu6sTMJrsyQ_D1c-d7bN2C_NV12b5_OI_Dt7PRycT5dfvl8sZgvp7biipaIbY2NoLVrDKFcuUpI0dqmdVJUitcMI9OwVmIqWIslMVQiTgRxnLHaIkmPwKet93ase9dYF0qiTt8m35u01tF4_fdN8Nf6Kt5pjBiRjKhi-PhkSPHH6PKge583nUxwccyaSKyIKN_ign74B72JYwqlX6EYFpQTSgo121I2xZyTa3dpMNKb6fRmOr2brjx4_2eHHf68VQHUFvjpO7f-j07PT1bzF_lvs_ul0w</recordid><startdate>202308</startdate><enddate>202308</enddate><creator>Kundu, Aritra Nath</creator><creator>Dougan, Carey E.</creator><creator>Mahmoud, Samar</creator><creator>Kilic, Alara</creator><creator>Panagiotou, Alexi</creator><creator>Richbourg, Nathan R.</creator><creator>Irakoze, Ninette</creator><creator>Peyton, Shelly R.</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8323-6745</orcidid><orcidid>https://orcid.org/0000-0002-5091-3321</orcidid><orcidid>https://orcid.org/0000-0002-7364-8727</orcidid><orcidid>https://orcid.org/0000-0002-2165-771X</orcidid><orcidid>https://orcid.org/0000-0001-5200-2153</orcidid></search><sort><creationdate>202308</creationdate><title>Tenascin‐C Activation of Lung Fibroblasts in a 3D Synthetic Lung Extracellular Matrix Mimic</title><author>Kundu, Aritra Nath ; Dougan, Carey E. ; Mahmoud, Samar ; Kilic, Alara ; Panagiotou, Alexi ; Richbourg, Nathan R. ; Irakoze, Ninette ; Peyton, Shelly R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4693-96fb1a73beda2369e4787fcdfe87496b510ad5f81375f182a3806272e655bc083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Binding</topic><topic>Biomechanics</topic><topic>Breast cancer</topic><topic>breast cancer metastasis</topic><topic>Breast Neoplasms</topic><topic>Combinatorial analysis</topic><topic>Extracellular matrix</topic><topic>Extracellular Matrix - metabolism</topic><topic>Female</topic><topic>Fibroblasts</topic><topic>Growth factors</topic><topic>Humans</topic><topic>Hydrogels</topic><topic>Hydrogels - chemistry</topic><topic>Integrins - metabolism</topic><topic>Lung</topic><topic>Lungs</topic><topic>Materials science</topic><topic>Matrix metalloproteinases</topic><topic>Metastasis</topic><topic>Peptides</topic><topic>Peptides - chemistry</topic><topic>poly(ethylene glycol)</topic><topic>stiffness</topic><topic>Structural integrity</topic><topic>Tenascin - metabolism</topic><topic>Tenascin - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kundu, Aritra Nath</creatorcontrib><creatorcontrib>Dougan, Carey E.</creatorcontrib><creatorcontrib>Mahmoud, Samar</creatorcontrib><creatorcontrib>Kilic, Alara</creatorcontrib><creatorcontrib>Panagiotou, Alexi</creatorcontrib><creatorcontrib>Richbourg, Nathan R.</creatorcontrib><creatorcontrib>Irakoze, Ninette</creatorcontrib><creatorcontrib>Peyton, Shelly R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Advanced materials (Weinheim)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kundu, Aritra Nath</au><au>Dougan, Carey E.</au><au>Mahmoud, Samar</au><au>Kilic, Alara</au><au>Panagiotou, Alexi</au><au>Richbourg, Nathan R.</au><au>Irakoze, Ninette</au><au>Peyton, Shelly R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tenascin‐C Activation of Lung Fibroblasts in a 3D Synthetic Lung Extracellular Matrix Mimic</atitle><jtitle>Advanced materials (Weinheim)</jtitle><addtitle>Adv Mater</addtitle><date>2023-08</date><risdate>2023</risdate><volume>35</volume><issue>33</issue><spage>e2301493</spage><epage>n/a</epage><pages>e2301493-n/a</pages><issn>0935-9648</issn><issn>1521-4095</issn><eissn>1521-4095</eissn><abstract>The lung extracellular matrix (ECM) maintains the structural integrity of the tissue and regulates the phenotype and functions of resident fibroblasts. Lung‐metastatic breast cancer alters these cell‐ECM interactions, promoting fibroblast activation. There is a need for bio‐instructive ECM models that match the ECM composition and biomechanics of the lung to study these cell‐matrix interactions in vitro. Here, a synthetic, bioactive hydrogel is synthesized that mimics the native lung modulus and includes a representative distribution of the most abundant ECM peptide motifs responsible for integrin‐binding and matrix metalloproteinase (MMP)‐mediated degradation in the lung, which enables quiescent culture of human lung fibroblasts (HLFs). Stimulation with transforming growth factor β1 (TGF‐β1), metastatic breast cancer conditioned media (CM), or tenascin‐C‐derived integrin‐binding peptide activated hydrogel‐encapsulated HLFs demonstrates multiple environmental methods to activate HLFs in a lung ECM‐mimicking hydrogel. This lung hydrogel platform is a tunable, synthetic approach to studying the independent and combinatorial effects of ECM in regulating fibroblast quiescence and activation.
A hydrogel that mimics the protein content and stiffness of healthy lung tissue is synthesized. Lung‐mimicking material is applied to reveal the ability of tenascin‐C to activate fibroblasts in lung‐metastatic breast cancer. This novel hydrogel environment will be incredibly useful for research questions involving the lung extracellular matrix.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>37227134</pmid><doi>10.1002/adma.202301493</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-8323-6745</orcidid><orcidid>https://orcid.org/0000-0002-5091-3321</orcidid><orcidid>https://orcid.org/0000-0002-7364-8727</orcidid><orcidid>https://orcid.org/0000-0002-2165-771X</orcidid><orcidid>https://orcid.org/0000-0001-5200-2153</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Binding Biomechanics Breast cancer breast cancer metastasis Breast Neoplasms Combinatorial analysis Extracellular matrix Extracellular Matrix - metabolism Female Fibroblasts Growth factors Humans Hydrogels Hydrogels - chemistry Integrins - metabolism Lung Lungs Materials science Matrix metalloproteinases Metastasis Peptides Peptides - chemistry poly(ethylene glycol) stiffness Structural integrity Tenascin - metabolism Tenascin - pharmacology |
title | Tenascin‐C Activation of Lung Fibroblasts in a 3D Synthetic Lung Extracellular Matrix Mimic |
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