Loading…

Biomaterial-embedded extracellular vesicles improve recovery of the dysfunctional myocardium

Extracellular vesicles (EV) are increasingly recognized as a therapeutic option in heart failure. They are usually administered by direct intramyocardial injections with the caveat of a rapid wash-out from the myocardium which might weaken their therapeutic efficacy. To improve their delivery in the...

Full description

Saved in:
Bibliographic Details
Published in:Biomaterials 2022-12, Vol.291, p.121877-121877, Article 121877
Main Authors: Pezzana, Chloé, Cras, Audrey, Simelière, Fanny, Guesdon, Rose, Desgres, Manon, Correa, Bruna Lima, Peuffier, Ashley, Bellamy, Valérie, Gouarderes, Sara, Alberdi, Antonio, Perier, Marie-Cécile, Pidial, Laetitia, Agnely, Florence, Bochot, Amélie, Hagège, Albert, Silvestre, Jean-Sébastien, Menasché, Philippe
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c443t-c883b1a0d5dfd98f754c23b651d7f9b997c12e903a3ca3700a63c9018beeb8343
cites cdi_FETCH-LOGICAL-c443t-c883b1a0d5dfd98f754c23b651d7f9b997c12e903a3ca3700a63c9018beeb8343
container_end_page 121877
container_issue
container_start_page 121877
container_title Biomaterials
container_volume 291
creator Pezzana, Chloé
Cras, Audrey
Simelière, Fanny
Guesdon, Rose
Desgres, Manon
Correa, Bruna Lima
Peuffier, Ashley
Bellamy, Valérie
Gouarderes, Sara
Alberdi, Antonio
Perier, Marie-Cécile
Pidial, Laetitia
Agnely, Florence
Bochot, Amélie
Hagège, Albert
Silvestre, Jean-Sébastien
Menasché, Philippe
description Extracellular vesicles (EV) are increasingly recognized as a therapeutic option in heart failure. They are usually administered by direct intramyocardial injections with the caveat of a rapid wash-out from the myocardium which might weaken their therapeutic efficacy. To improve their delivery in the failing myocardium, we designed a system consisting of loading EV into a clinical-grade hyaluronic acid (HA) biomaterial. EV were isolated from umbilical cord-derived mesenchymal stromal cells. The suitability of HA as a delivery platform was then assessed in vitro. Rheology studies demonstrated the viscoelastic and shear thinning behaviors of the selected HA allowing its easy injection. Moreover, the release of HA-embedded EV was sustained over more than 10 days, and EV bioactivity was not altered by the biomaterial. In a rat model of myocardial ischemia reperfusion, we showed that HA-embedded EV preserved cardiac function (echocardiography), improved angiogenesis and decreased both apoptosis and fibrosis (histology and transcriptomics) when compared to intramyocardial administration of EV alone. These data thus strengthen the concept that inclusion of EV into a clinically useable biomaterial might optimize their beneficial effects on post-ischemic cardiac repair.
doi_str_mv 10.1016/j.biomaterials.2022.121877
format article
fullrecord <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_04317724v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0142961222005178</els_id><sourcerecordid>2734612363</sourcerecordid><originalsourceid>FETCH-LOGICAL-c443t-c883b1a0d5dfd98f754c23b651d7f9b997c12e903a3ca3700a63c9018beeb8343</originalsourceid><addsrcrecordid>eNqNkF1LwzAYhYMoOKf_oXilF635atN6N-fHhIE3eieENHnLMtplJu1w_96Minrp1eEN5xxyHoQuCc4IJsXNOqut61QP3qo2ZBRTmhFKSiGO0CRKmeYVzo_RBBNO06og9BSdhbDG8cacTtD73W8-ha4GY8Ak8Nl7paFth1b5ZAfB6hZCYrutdztIPOgofp-4JulXkJh9aIaN7q3bqDbp9k4rb-zQnaOTJn4LLr51it4eH17ni3T58vQ8ny1TzTnrU12WrCYKm9w0piobkXNNWV3kxIimqqtKaEKhwkwxrZjAWBVMV5iUNUBdMs6m6HrsXalWbr3tlN9Lp6xczJby8IY5I0JQviPRezV645SPAUIvOxsOU9UG3BAkFYxHTKxg0Xo7WrV3IXhofroJlgf8ci3_4pcH_HLEH8P3Yxji8J0FL4O2sNFgbMTXS-Psf2q-AF-Mln4</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2734612363</pqid></control><display><type>article</type><title>Biomaterial-embedded extracellular vesicles improve recovery of the dysfunctional myocardium</title><source>ScienceDirect Freedom Collection</source><creator>Pezzana, Chloé ; Cras, Audrey ; Simelière, Fanny ; Guesdon, Rose ; Desgres, Manon ; Correa, Bruna Lima ; Peuffier, Ashley ; Bellamy, Valérie ; Gouarderes, Sara ; Alberdi, Antonio ; Perier, Marie-Cécile ; Pidial, Laetitia ; Agnely, Florence ; Bochot, Amélie ; Hagège, Albert ; Silvestre, Jean-Sébastien ; Menasché, Philippe</creator><creatorcontrib>Pezzana, Chloé ; Cras, Audrey ; Simelière, Fanny ; Guesdon, Rose ; Desgres, Manon ; Correa, Bruna Lima ; Peuffier, Ashley ; Bellamy, Valérie ; Gouarderes, Sara ; Alberdi, Antonio ; Perier, Marie-Cécile ; Pidial, Laetitia ; Agnely, Florence ; Bochot, Amélie ; Hagège, Albert ; Silvestre, Jean-Sébastien ; Menasché, Philippe</creatorcontrib><description>Extracellular vesicles (EV) are increasingly recognized as a therapeutic option in heart failure. They are usually administered by direct intramyocardial injections with the caveat of a rapid wash-out from the myocardium which might weaken their therapeutic efficacy. To improve their delivery in the failing myocardium, we designed a system consisting of loading EV into a clinical-grade hyaluronic acid (HA) biomaterial. EV were isolated from umbilical cord-derived mesenchymal stromal cells. The suitability of HA as a delivery platform was then assessed in vitro. Rheology studies demonstrated the viscoelastic and shear thinning behaviors of the selected HA allowing its easy injection. Moreover, the release of HA-embedded EV was sustained over more than 10 days, and EV bioactivity was not altered by the biomaterial. In a rat model of myocardial ischemia reperfusion, we showed that HA-embedded EV preserved cardiac function (echocardiography), improved angiogenesis and decreased both apoptosis and fibrosis (histology and transcriptomics) when compared to intramyocardial administration of EV alone. These data thus strengthen the concept that inclusion of EV into a clinically useable biomaterial might optimize their beneficial effects on post-ischemic cardiac repair.</description><identifier>ISSN: 0142-9612</identifier><identifier>EISSN: 1878-5905</identifier><identifier>DOI: 10.1016/j.biomaterials.2022.121877</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Cardiac repair ; Extracellular vesicles ; Heart failure ; Injectable biomaterial ; Life Sciences ; Mesenchymal stromal cells ; Myocardial ischemia-reperfusion</subject><ispartof>Biomaterials, 2022-12, Vol.291, p.121877-121877, Article 121877</ispartof><rights>2022 Elsevier Ltd</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-c883b1a0d5dfd98f754c23b651d7f9b997c12e903a3ca3700a63c9018beeb8343</citedby><cites>FETCH-LOGICAL-c443t-c883b1a0d5dfd98f754c23b651d7f9b997c12e903a3ca3700a63c9018beeb8343</cites><orcidid>0000-0003-4674-7970 ; 0000-0001-6333-4073 ; 0000-0001-9080-7876 ; 0000-0002-6894-9584 ; 0000-0003-2777-9010 ; 0000-0001-7940-4216</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://hal.science/hal-04317724$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Pezzana, Chloé</creatorcontrib><creatorcontrib>Cras, Audrey</creatorcontrib><creatorcontrib>Simelière, Fanny</creatorcontrib><creatorcontrib>Guesdon, Rose</creatorcontrib><creatorcontrib>Desgres, Manon</creatorcontrib><creatorcontrib>Correa, Bruna Lima</creatorcontrib><creatorcontrib>Peuffier, Ashley</creatorcontrib><creatorcontrib>Bellamy, Valérie</creatorcontrib><creatorcontrib>Gouarderes, Sara</creatorcontrib><creatorcontrib>Alberdi, Antonio</creatorcontrib><creatorcontrib>Perier, Marie-Cécile</creatorcontrib><creatorcontrib>Pidial, Laetitia</creatorcontrib><creatorcontrib>Agnely, Florence</creatorcontrib><creatorcontrib>Bochot, Amélie</creatorcontrib><creatorcontrib>Hagège, Albert</creatorcontrib><creatorcontrib>Silvestre, Jean-Sébastien</creatorcontrib><creatorcontrib>Menasché, Philippe</creatorcontrib><title>Biomaterial-embedded extracellular vesicles improve recovery of the dysfunctional myocardium</title><title>Biomaterials</title><description>Extracellular vesicles (EV) are increasingly recognized as a therapeutic option in heart failure. They are usually administered by direct intramyocardial injections with the caveat of a rapid wash-out from the myocardium which might weaken their therapeutic efficacy. To improve their delivery in the failing myocardium, we designed a system consisting of loading EV into a clinical-grade hyaluronic acid (HA) biomaterial. EV were isolated from umbilical cord-derived mesenchymal stromal cells. The suitability of HA as a delivery platform was then assessed in vitro. Rheology studies demonstrated the viscoelastic and shear thinning behaviors of the selected HA allowing its easy injection. Moreover, the release of HA-embedded EV was sustained over more than 10 days, and EV bioactivity was not altered by the biomaterial. In a rat model of myocardial ischemia reperfusion, we showed that HA-embedded EV preserved cardiac function (echocardiography), improved angiogenesis and decreased both apoptosis and fibrosis (histology and transcriptomics) when compared to intramyocardial administration of EV alone. These data thus strengthen the concept that inclusion of EV into a clinically useable biomaterial might optimize their beneficial effects on post-ischemic cardiac repair.</description><subject>Cardiac repair</subject><subject>Extracellular vesicles</subject><subject>Heart failure</subject><subject>Injectable biomaterial</subject><subject>Life Sciences</subject><subject>Mesenchymal stromal cells</subject><subject>Myocardial ischemia-reperfusion</subject><issn>0142-9612</issn><issn>1878-5905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqNkF1LwzAYhYMoOKf_oXilF635atN6N-fHhIE3eieENHnLMtplJu1w_96Minrp1eEN5xxyHoQuCc4IJsXNOqut61QP3qo2ZBRTmhFKSiGO0CRKmeYVzo_RBBNO06og9BSdhbDG8cacTtD73W8-ha4GY8Ak8Nl7paFth1b5ZAfB6hZCYrutdztIPOgofp-4JulXkJh9aIaN7q3bqDbp9k4rb-zQnaOTJn4LLr51it4eH17ni3T58vQ8ny1TzTnrU12WrCYKm9w0piobkXNNWV3kxIimqqtKaEKhwkwxrZjAWBVMV5iUNUBdMs6m6HrsXalWbr3tlN9Lp6xczJby8IY5I0JQviPRezV645SPAUIvOxsOU9UG3BAkFYxHTKxg0Xo7WrV3IXhofroJlgf8ci3_4pcH_HLEH8P3Yxji8J0FL4O2sNFgbMTXS-Psf2q-AF-Mln4</recordid><startdate>202212</startdate><enddate>202212</enddate><creator>Pezzana, Chloé</creator><creator>Cras, Audrey</creator><creator>Simelière, Fanny</creator><creator>Guesdon, Rose</creator><creator>Desgres, Manon</creator><creator>Correa, Bruna Lima</creator><creator>Peuffier, Ashley</creator><creator>Bellamy, Valérie</creator><creator>Gouarderes, Sara</creator><creator>Alberdi, Antonio</creator><creator>Perier, Marie-Cécile</creator><creator>Pidial, Laetitia</creator><creator>Agnely, Florence</creator><creator>Bochot, Amélie</creator><creator>Hagège, Albert</creator><creator>Silvestre, Jean-Sébastien</creator><creator>Menasché, Philippe</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-4674-7970</orcidid><orcidid>https://orcid.org/0000-0001-6333-4073</orcidid><orcidid>https://orcid.org/0000-0001-9080-7876</orcidid><orcidid>https://orcid.org/0000-0002-6894-9584</orcidid><orcidid>https://orcid.org/0000-0003-2777-9010</orcidid><orcidid>https://orcid.org/0000-0001-7940-4216</orcidid></search><sort><creationdate>202212</creationdate><title>Biomaterial-embedded extracellular vesicles improve recovery of the dysfunctional myocardium</title><author>Pezzana, Chloé ; Cras, Audrey ; Simelière, Fanny ; Guesdon, Rose ; Desgres, Manon ; Correa, Bruna Lima ; Peuffier, Ashley ; Bellamy, Valérie ; Gouarderes, Sara ; Alberdi, Antonio ; Perier, Marie-Cécile ; Pidial, Laetitia ; Agnely, Florence ; Bochot, Amélie ; Hagège, Albert ; Silvestre, Jean-Sébastien ; Menasché, Philippe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-c883b1a0d5dfd98f754c23b651d7f9b997c12e903a3ca3700a63c9018beeb8343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Cardiac repair</topic><topic>Extracellular vesicles</topic><topic>Heart failure</topic><topic>Injectable biomaterial</topic><topic>Life Sciences</topic><topic>Mesenchymal stromal cells</topic><topic>Myocardial ischemia-reperfusion</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pezzana, Chloé</creatorcontrib><creatorcontrib>Cras, Audrey</creatorcontrib><creatorcontrib>Simelière, Fanny</creatorcontrib><creatorcontrib>Guesdon, Rose</creatorcontrib><creatorcontrib>Desgres, Manon</creatorcontrib><creatorcontrib>Correa, Bruna Lima</creatorcontrib><creatorcontrib>Peuffier, Ashley</creatorcontrib><creatorcontrib>Bellamy, Valérie</creatorcontrib><creatorcontrib>Gouarderes, Sara</creatorcontrib><creatorcontrib>Alberdi, Antonio</creatorcontrib><creatorcontrib>Perier, Marie-Cécile</creatorcontrib><creatorcontrib>Pidial, Laetitia</creatorcontrib><creatorcontrib>Agnely, Florence</creatorcontrib><creatorcontrib>Bochot, Amélie</creatorcontrib><creatorcontrib>Hagège, Albert</creatorcontrib><creatorcontrib>Silvestre, Jean-Sébastien</creatorcontrib><creatorcontrib>Menasché, Philippe</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pezzana, Chloé</au><au>Cras, Audrey</au><au>Simelière, Fanny</au><au>Guesdon, Rose</au><au>Desgres, Manon</au><au>Correa, Bruna Lima</au><au>Peuffier, Ashley</au><au>Bellamy, Valérie</au><au>Gouarderes, Sara</au><au>Alberdi, Antonio</au><au>Perier, Marie-Cécile</au><au>Pidial, Laetitia</au><au>Agnely, Florence</au><au>Bochot, Amélie</au><au>Hagège, Albert</au><au>Silvestre, Jean-Sébastien</au><au>Menasché, Philippe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biomaterial-embedded extracellular vesicles improve recovery of the dysfunctional myocardium</atitle><jtitle>Biomaterials</jtitle><date>2022-12</date><risdate>2022</risdate><volume>291</volume><spage>121877</spage><epage>121877</epage><pages>121877-121877</pages><artnum>121877</artnum><issn>0142-9612</issn><eissn>1878-5905</eissn><abstract>Extracellular vesicles (EV) are increasingly recognized as a therapeutic option in heart failure. They are usually administered by direct intramyocardial injections with the caveat of a rapid wash-out from the myocardium which might weaken their therapeutic efficacy. To improve their delivery in the failing myocardium, we designed a system consisting of loading EV into a clinical-grade hyaluronic acid (HA) biomaterial. EV were isolated from umbilical cord-derived mesenchymal stromal cells. The suitability of HA as a delivery platform was then assessed in vitro. Rheology studies demonstrated the viscoelastic and shear thinning behaviors of the selected HA allowing its easy injection. Moreover, the release of HA-embedded EV was sustained over more than 10 days, and EV bioactivity was not altered by the biomaterial. In a rat model of myocardial ischemia reperfusion, we showed that HA-embedded EV preserved cardiac function (echocardiography), improved angiogenesis and decreased both apoptosis and fibrosis (histology and transcriptomics) when compared to intramyocardial administration of EV alone. These data thus strengthen the concept that inclusion of EV into a clinically useable biomaterial might optimize their beneficial effects on post-ischemic cardiac repair.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.biomaterials.2022.121877</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-4674-7970</orcidid><orcidid>https://orcid.org/0000-0001-6333-4073</orcidid><orcidid>https://orcid.org/0000-0001-9080-7876</orcidid><orcidid>https://orcid.org/0000-0002-6894-9584</orcidid><orcidid>https://orcid.org/0000-0003-2777-9010</orcidid><orcidid>https://orcid.org/0000-0001-7940-4216</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0142-9612
ispartof Biomaterials, 2022-12, Vol.291, p.121877-121877, Article 121877
issn 0142-9612
1878-5905
language eng
recordid cdi_hal_primary_oai_HAL_hal_04317724v1
source ScienceDirect Freedom Collection
subjects Cardiac repair
Extracellular vesicles
Heart failure
Injectable biomaterial
Life Sciences
Mesenchymal stromal cells
Myocardial ischemia-reperfusion
title Biomaterial-embedded extracellular vesicles improve recovery of the dysfunctional myocardium
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T21%3A54%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Biomaterial-embedded%20extracellular%20vesicles%20improve%20recovery%20of%20the%20dysfunctional%20myocardium&rft.jtitle=Biomaterials&rft.au=Pezzana,%20Chlo%C3%A9&rft.date=2022-12&rft.volume=291&rft.spage=121877&rft.epage=121877&rft.pages=121877-121877&rft.artnum=121877&rft.issn=0142-9612&rft.eissn=1878-5905&rft_id=info:doi/10.1016/j.biomaterials.2022.121877&rft_dat=%3Cproquest_hal_p%3E2734612363%3C/proquest_hal_p%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c443t-c883b1a0d5dfd98f754c23b651d7f9b997c12e903a3ca3700a63c9018beeb8343%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2734612363&rft_id=info:pmid/&rfr_iscdi=true