Adiponectin stimulates exosome release to enhance mesenchymal stem cell driven therapy of heart failure in mice

Mesenchymal stem/stromal cells (MSCs) are cultured adult stem cells originally reside in virtually all tissues and the gain of MSCs by transplantation has become the leading form of cell therapy in various diseases. However, there is limited knowledge on the alteration of its efficacy by factors in...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Nakamura, Yuto, Kita, Shunbun, Tanaka, Yoshimitsu, Fukuda, Shiro, Obata, Yoshinari, Okita, Tomonori, Nishida, Hiroyuki, Takahashi, Yuki, Kawachi, Yuusuke, Tsugawa-Shimizu, Yuri, Fujishima, Yuya, Nishizawa, Hitoshi, Takakura, Yoshinobu, Miyagawa, Shigeru, Sawa, Yoshiki, Maeda, Norikazu, Shimomura, Iichiro
Format: Dataset
Sprache:eng
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator Nakamura, Yuto
Kita, Shunbun
Tanaka, Yoshimitsu
Fukuda, Shiro
Obata, Yoshinari
Okita, Tomonori
Nishida, Hiroyuki
Takahashi, Yuki
Kawachi, Yuusuke
Tsugawa-Shimizu, Yuri
Fujishima, Yuya
Nishizawa, Hitoshi
Takakura, Yoshinobu
Miyagawa, Shigeru
Sawa, Yoshiki
Maeda, Norikazu
Shimomura, Iichiro
description Mesenchymal stem/stromal cells (MSCs) are cultured adult stem cells originally reside in virtually all tissues and the gain of MSCs by transplantation has become the leading form of cell therapy in various diseases. However, there is limited knowledge on the alteration of its efficacy by factors in recipients. Here we report that the cardioprotective properties of intravenously injected MSCs in a mouse model of pressure-overload heart failure largely depend on circulating adiponectin, an adipocyte secreted factor. The injected MSCs exerted their function through exosomes, extracellular vesicles of endosome-origin. Adiponectin stimulated exosome biogenesis and secretion through binding to T-cadherin, a unique glycosylphosphatidylinositol-anchored cadherin, on MSCs. A pharmacological or adenovirus-mediated genetic increase in plasma adiponectin enhanced the therapeutic efficacy of MSCs. Our findings provide novel insights into the importance of adiponectin in mesenchymal progenitors-mediated organ protections.
doi_str_mv 10.5061/dryad.t76hdr7xq
format Dataset
fullrecord <record><control><sourceid>datacite_PQ8</sourceid><recordid>TN_cdi_datacite_primary_10_5061_dryad_t76hdr7xq</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_5061_dryad_t76hdr7xq</sourcerecordid><originalsourceid>FETCH-datacite_primary_10_5061_dryad_t76hdr7xq3</originalsourceid><addsrcrecordid>eNqVzrtuAjEQhWE3FIikpp0XAHYVBeooAvEA6a2RfVa25MsyHhD79lyE6FOd6j_6jFn23fq72_YbLxP7te62wcvuepqb-uPjWAucxkJNYz4nVjTCtbaaQYIEbiCthBK4OFBGQ3FhypzuBTI5pERe4gWFNEB4nKgOFMCiNHBMZwHd73N0-DCzgVPD52sXZnPY__0eV56VXVTYUWJmmWzf2QfZPsn2Tf76f3EDmLRXAQ</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>dataset</recordtype></control><display><type>dataset</type><title>Adiponectin stimulates exosome release to enhance mesenchymal stem cell driven therapy of heart failure in mice</title><source>DataCite</source><creator>Nakamura, Yuto ; Kita, Shunbun ; Tanaka, Yoshimitsu ; Fukuda, Shiro ; Obata, Yoshinari ; Okita, Tomonori ; Nishida, Hiroyuki ; Takahashi, Yuki ; Kawachi, Yuusuke ; Tsugawa-Shimizu, Yuri ; Fujishima, Yuya ; Nishizawa, Hitoshi ; Takakura, Yoshinobu ; Miyagawa, Shigeru ; Sawa, Yoshiki ; Maeda, Norikazu ; Shimomura, Iichiro</creator><creatorcontrib>Nakamura, Yuto ; Kita, Shunbun ; Tanaka, Yoshimitsu ; Fukuda, Shiro ; Obata, Yoshinari ; Okita, Tomonori ; Nishida, Hiroyuki ; Takahashi, Yuki ; Kawachi, Yuusuke ; Tsugawa-Shimizu, Yuri ; Fujishima, Yuya ; Nishizawa, Hitoshi ; Takakura, Yoshinobu ; Miyagawa, Shigeru ; Sawa, Yoshiki ; Maeda, Norikazu ; Shimomura, Iichiro</creatorcontrib><description>Mesenchymal stem/stromal cells (MSCs) are cultured adult stem cells originally reside in virtually all tissues and the gain of MSCs by transplantation has become the leading form of cell therapy in various diseases. However, there is limited knowledge on the alteration of its efficacy by factors in recipients. Here we report that the cardioprotective properties of intravenously injected MSCs in a mouse model of pressure-overload heart failure largely depend on circulating adiponectin, an adipocyte secreted factor. The injected MSCs exerted their function through exosomes, extracellular vesicles of endosome-origin. Adiponectin stimulated exosome biogenesis and secretion through binding to T-cadherin, a unique glycosylphosphatidylinositol-anchored cadherin, on MSCs. A pharmacological or adenovirus-mediated genetic increase in plasma adiponectin enhanced the therapeutic efficacy of MSCs. Our findings provide novel insights into the importance of adiponectin in mesenchymal progenitors-mediated organ protections.</description><identifier>DOI: 10.5061/dryad.t76hdr7xq</identifier><language>eng</language><publisher>Dryad</publisher><creationdate>2020</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-8937-0053 ; 0000-0002-8937-0053</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,1892</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.5061/dryad.t76hdr7xq$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Nakamura, Yuto</creatorcontrib><creatorcontrib>Kita, Shunbun</creatorcontrib><creatorcontrib>Tanaka, Yoshimitsu</creatorcontrib><creatorcontrib>Fukuda, Shiro</creatorcontrib><creatorcontrib>Obata, Yoshinari</creatorcontrib><creatorcontrib>Okita, Tomonori</creatorcontrib><creatorcontrib>Nishida, Hiroyuki</creatorcontrib><creatorcontrib>Takahashi, Yuki</creatorcontrib><creatorcontrib>Kawachi, Yuusuke</creatorcontrib><creatorcontrib>Tsugawa-Shimizu, Yuri</creatorcontrib><creatorcontrib>Fujishima, Yuya</creatorcontrib><creatorcontrib>Nishizawa, Hitoshi</creatorcontrib><creatorcontrib>Takakura, Yoshinobu</creatorcontrib><creatorcontrib>Miyagawa, Shigeru</creatorcontrib><creatorcontrib>Sawa, Yoshiki</creatorcontrib><creatorcontrib>Maeda, Norikazu</creatorcontrib><creatorcontrib>Shimomura, Iichiro</creatorcontrib><title>Adiponectin stimulates exosome release to enhance mesenchymal stem cell driven therapy of heart failure in mice</title><description>Mesenchymal stem/stromal cells (MSCs) are cultured adult stem cells originally reside in virtually all tissues and the gain of MSCs by transplantation has become the leading form of cell therapy in various diseases. However, there is limited knowledge on the alteration of its efficacy by factors in recipients. Here we report that the cardioprotective properties of intravenously injected MSCs in a mouse model of pressure-overload heart failure largely depend on circulating adiponectin, an adipocyte secreted factor. The injected MSCs exerted their function through exosomes, extracellular vesicles of endosome-origin. Adiponectin stimulated exosome biogenesis and secretion through binding to T-cadherin, a unique glycosylphosphatidylinositol-anchored cadherin, on MSCs. A pharmacological or adenovirus-mediated genetic increase in plasma adiponectin enhanced the therapeutic efficacy of MSCs. Our findings provide novel insights into the importance of adiponectin in mesenchymal progenitors-mediated organ protections.</description><fulltext>true</fulltext><rsrctype>dataset</rsrctype><creationdate>2020</creationdate><recordtype>dataset</recordtype><sourceid>PQ8</sourceid><recordid>eNqVzrtuAjEQhWE3FIikpp0XAHYVBeooAvEA6a2RfVa25MsyHhD79lyE6FOd6j_6jFn23fq72_YbLxP7te62wcvuepqb-uPjWAucxkJNYz4nVjTCtbaaQYIEbiCthBK4OFBGQ3FhypzuBTI5pERe4gWFNEB4nKgOFMCiNHBMZwHd73N0-DCzgVPD52sXZnPY__0eV56VXVTYUWJmmWzf2QfZPsn2Tf76f3EDmLRXAQ</recordid><startdate>20200921</startdate><enddate>20200921</enddate><creator>Nakamura, Yuto</creator><creator>Kita, Shunbun</creator><creator>Tanaka, Yoshimitsu</creator><creator>Fukuda, Shiro</creator><creator>Obata, Yoshinari</creator><creator>Okita, Tomonori</creator><creator>Nishida, Hiroyuki</creator><creator>Takahashi, Yuki</creator><creator>Kawachi, Yuusuke</creator><creator>Tsugawa-Shimizu, Yuri</creator><creator>Fujishima, Yuya</creator><creator>Nishizawa, Hitoshi</creator><creator>Takakura, Yoshinobu</creator><creator>Miyagawa, Shigeru</creator><creator>Sawa, Yoshiki</creator><creator>Maeda, Norikazu</creator><creator>Shimomura, Iichiro</creator><general>Dryad</general><scope>DYCCY</scope><scope>PQ8</scope><orcidid>https://orcid.org/0000-0002-8937-0053</orcidid><orcidid>https://orcid.org/0000-0002-8937-0053</orcidid></search><sort><creationdate>20200921</creationdate><title>Adiponectin stimulates exosome release to enhance mesenchymal stem cell driven therapy of heart failure in mice</title><author>Nakamura, Yuto ; Kita, Shunbun ; Tanaka, Yoshimitsu ; Fukuda, Shiro ; Obata, Yoshinari ; Okita, Tomonori ; Nishida, Hiroyuki ; Takahashi, Yuki ; Kawachi, Yuusuke ; Tsugawa-Shimizu, Yuri ; Fujishima, Yuya ; Nishizawa, Hitoshi ; Takakura, Yoshinobu ; Miyagawa, Shigeru ; Sawa, Yoshiki ; Maeda, Norikazu ; Shimomura, Iichiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-datacite_primary_10_5061_dryad_t76hdr7xq3</frbrgroupid><rsrctype>datasets</rsrctype><prefilter>datasets</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Nakamura, Yuto</creatorcontrib><creatorcontrib>Kita, Shunbun</creatorcontrib><creatorcontrib>Tanaka, Yoshimitsu</creatorcontrib><creatorcontrib>Fukuda, Shiro</creatorcontrib><creatorcontrib>Obata, Yoshinari</creatorcontrib><creatorcontrib>Okita, Tomonori</creatorcontrib><creatorcontrib>Nishida, Hiroyuki</creatorcontrib><creatorcontrib>Takahashi, Yuki</creatorcontrib><creatorcontrib>Kawachi, Yuusuke</creatorcontrib><creatorcontrib>Tsugawa-Shimizu, Yuri</creatorcontrib><creatorcontrib>Fujishima, Yuya</creatorcontrib><creatorcontrib>Nishizawa, Hitoshi</creatorcontrib><creatorcontrib>Takakura, Yoshinobu</creatorcontrib><creatorcontrib>Miyagawa, Shigeru</creatorcontrib><creatorcontrib>Sawa, Yoshiki</creatorcontrib><creatorcontrib>Maeda, Norikazu</creatorcontrib><creatorcontrib>Shimomura, Iichiro</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Nakamura, Yuto</au><au>Kita, Shunbun</au><au>Tanaka, Yoshimitsu</au><au>Fukuda, Shiro</au><au>Obata, Yoshinari</au><au>Okita, Tomonori</au><au>Nishida, Hiroyuki</au><au>Takahashi, Yuki</au><au>Kawachi, Yuusuke</au><au>Tsugawa-Shimizu, Yuri</au><au>Fujishima, Yuya</au><au>Nishizawa, Hitoshi</au><au>Takakura, Yoshinobu</au><au>Miyagawa, Shigeru</au><au>Sawa, Yoshiki</au><au>Maeda, Norikazu</au><au>Shimomura, Iichiro</au><format>book</format><genre>unknown</genre><ristype>DATA</ristype><title>Adiponectin stimulates exosome release to enhance mesenchymal stem cell driven therapy of heart failure in mice</title><date>2020-09-21</date><risdate>2020</risdate><abstract>Mesenchymal stem/stromal cells (MSCs) are cultured adult stem cells originally reside in virtually all tissues and the gain of MSCs by transplantation has become the leading form of cell therapy in various diseases. However, there is limited knowledge on the alteration of its efficacy by factors in recipients. Here we report that the cardioprotective properties of intravenously injected MSCs in a mouse model of pressure-overload heart failure largely depend on circulating adiponectin, an adipocyte secreted factor. The injected MSCs exerted their function through exosomes, extracellular vesicles of endosome-origin. Adiponectin stimulated exosome biogenesis and secretion through binding to T-cadherin, a unique glycosylphosphatidylinositol-anchored cadherin, on MSCs. A pharmacological or adenovirus-mediated genetic increase in plasma adiponectin enhanced the therapeutic efficacy of MSCs. Our findings provide novel insights into the importance of adiponectin in mesenchymal progenitors-mediated organ protections.</abstract><pub>Dryad</pub><doi>10.5061/dryad.t76hdr7xq</doi><orcidid>https://orcid.org/0000-0002-8937-0053</orcidid><orcidid>https://orcid.org/0000-0002-8937-0053</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier DOI: 10.5061/dryad.t76hdr7xq
ispartof
issn
language eng
recordid cdi_datacite_primary_10_5061_dryad_t76hdr7xq
source DataCite
title Adiponectin stimulates exosome release to enhance mesenchymal stem cell driven therapy of heart failure in mice
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T15%3A04%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-datacite_PQ8&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=unknown&rft.au=Nakamura,%20Yuto&rft.date=2020-09-21&rft_id=info:doi/10.5061/dryad.t76hdr7xq&rft_dat=%3Cdatacite_PQ8%3E10_5061_dryad_t76hdr7xq%3C/datacite_PQ8%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true