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A scalable culture system incorporating microcarrier for specialised mesenchymal stem cells from human embryonic stem cells
Mesenchymal stromal cells (MSCs) derived from human embryonic stem cells (hESCs) are a desirable cell source for cell therapy owing to their capacity to be produced stably and homogeneously in large quantities. However, a scalable culture system for hPSC-derived MSCs is urgently needed to meet the c...
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Published in: | Materials today bio 2023-06, Vol.20, p.100662-100662, Article 100662 |
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creator | Gao, Tingting Zhao, Xiyuan Hao, Jie Tian, Yao Ma, Huike Liu, Wenjing An, Bin Sun, Faguo Liu, Shasha Guo, Baojie Niu, Shuaishuai Li, Zhongwen Wang, Chenxin Wang, Yukai Feng, Guihai Wang, Liu Li, Wei Wu, Jun Guo, Meijin Zhou, Qi Gu, Qi |
description | Mesenchymal stromal cells (MSCs) derived from human embryonic stem cells (hESCs) are a desirable cell source for cell therapy owing to their capacity to be produced stably and homogeneously in large quantities. However, a scalable culture system for hPSC-derived MSCs is urgently needed to meet the cell quantity and quality requirements of practical clinical applications. In this study, we developed a new microcarrier with hyaluronic acid (HA) as the core material, which allowed scalable serum-free suspension culture of hESC-derived MSCs (IMRCs). We used optimal microcarriers with a coating collagen concentration of 100 μg/mL or concave-structured surface (cHAMCs) for IMRC amplification in a stirred bioreactor, expanding IMRCs within six days with the highest yield of over one million cells per milliliter. In addition, the harvested cells exhibited high viability, immunomodulatory and regenerative therapeutic promise comparable to monolayer cultured MSCs while showing more increased secretion of extracellular matrix (ECM), particularly collagen-related proteins. In summary, we have established a scalable culture system for hESC-MSCs, providing novel approaches for future cell therapies.
Gu et al. have developed a novel hyaluronic acid microcarrier (HAMC) for scalable suspension serum-free culture of mesenchymal stromal cells derived from human embryonic stem cells (IMRCs) in bioreactor-based systems. The cHAMC, with a concave structure, showed superior cell attachment and expansion capabilities, resulting in higher cell yields without compromising cell proliferation, stemness characteristics, or immunomodulatory properties. These findings demonstrate the potential of HAMC and cHAMCs as promising candidates for future cell-based therapies, providing a cost-effective solution for large-scale cell production. [Display omitted]
•A novel HA-based microcarrier HAMC as the core material was successfully used for the scalable suspension serum-free culture of hESC-derived MSCs.•The expanded cells maintained their stemness characteristics and immunomodulatory properties.•The newly developed cHAMC showed superior cell attachment and expansion capabilities, leading to higher cell yield. |
doi_str_mv | 10.1016/j.mtbio.2023.100662 |
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fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_45d9852f184b411cae02c96890caf26b</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S2590006423001229</els_id><doaj_id>oai_doaj_org_article_45d9852f184b411cae02c96890caf26b</doaj_id><sourcerecordid>2818056566</sourcerecordid><originalsourceid>FETCH-LOGICAL-c476t-b8f05dd2e4b0b360e6f098b622687503884633e83734d749267968e09143982d3</originalsourceid><addsrcrecordid>eNp9kstq3DAUhk1paUKaJygULbuZ6dHFsrwoJYReAoFu2rWQ5OMZDZY1lezAkJevZpyGyaYrSefyHfH_p6reU1hToPLTbh0m6-OaAeMlAlKyV9Ulq1tYlYd4fXa_qK5z3gEAa1oB0L6tLnjDqKhFc1k93pDszGDsgMTNwzQnJPmQJwzEjy6mfUxm8uOGBO9SdCYlj4n0MZG8R-fN4DN2JGDG0W0PwQzk1OtwGDLpUwxkOwczEgw2HeLo3Vn-XfWmN0PG66fzqvr97euv2x-r-5_f725v7ldONHJaWdVD3XUMhQXLJaDsoVVWMiZVUwNXSkjOUfGGi64RLZNNKxVCSwVvFev4VXW3cLtodnqffDDpoKPx-hSIaaNNmrwbUIu6a1XNeqqEFZQ6g8BcobXgTM-kLawvC2s_24Cdw3FKZngBfZkZ_VZv4oMurhWOhEL4-ERI8c-MedLB56MeZsQ4Z80UVVDLWspSypfSIn3OCfvnORSOQKl3-rQG-rgGelmD0vXh_IvPPf9MLwWflwIsoj8UP3V2vviHnU_opqKK_--Av4XNxeI</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2818056566</pqid></control><display><type>article</type><title>A scalable culture system incorporating microcarrier for specialised mesenchymal stem cells from human embryonic stem cells</title><source>Open Access: PubMed Central</source><source>ScienceDirect Journals</source><creator>Gao, Tingting ; Zhao, Xiyuan ; Hao, Jie ; Tian, Yao ; Ma, Huike ; Liu, Wenjing ; An, Bin ; Sun, Faguo ; Liu, Shasha ; Guo, Baojie ; Niu, Shuaishuai ; Li, Zhongwen ; Wang, Chenxin ; Wang, Yukai ; Feng, Guihai ; Wang, Liu ; Li, Wei ; Wu, Jun ; Guo, Meijin ; Zhou, Qi ; Gu, Qi</creator><creatorcontrib>Gao, Tingting ; Zhao, Xiyuan ; Hao, Jie ; Tian, Yao ; Ma, Huike ; Liu, Wenjing ; An, Bin ; Sun, Faguo ; Liu, Shasha ; Guo, Baojie ; Niu, Shuaishuai ; Li, Zhongwen ; Wang, Chenxin ; Wang, Yukai ; Feng, Guihai ; Wang, Liu ; Li, Wei ; Wu, Jun ; Guo, Meijin ; Zhou, Qi ; Gu, Qi</creatorcontrib><description>Mesenchymal stromal cells (MSCs) derived from human embryonic stem cells (hESCs) are a desirable cell source for cell therapy owing to their capacity to be produced stably and homogeneously in large quantities. However, a scalable culture system for hPSC-derived MSCs is urgently needed to meet the cell quantity and quality requirements of practical clinical applications. In this study, we developed a new microcarrier with hyaluronic acid (HA) as the core material, which allowed scalable serum-free suspension culture of hESC-derived MSCs (IMRCs). We used optimal microcarriers with a coating collagen concentration of 100 μg/mL or concave-structured surface (cHAMCs) for IMRC amplification in a stirred bioreactor, expanding IMRCs within six days with the highest yield of over one million cells per milliliter. In addition, the harvested cells exhibited high viability, immunomodulatory and regenerative therapeutic promise comparable to monolayer cultured MSCs while showing more increased secretion of extracellular matrix (ECM), particularly collagen-related proteins. In summary, we have established a scalable culture system for hESC-MSCs, providing novel approaches for future cell therapies.
Gu et al. have developed a novel hyaluronic acid microcarrier (HAMC) for scalable suspension serum-free culture of mesenchymal stromal cells derived from human embryonic stem cells (IMRCs) in bioreactor-based systems. The cHAMC, with a concave structure, showed superior cell attachment and expansion capabilities, resulting in higher cell yields without compromising cell proliferation, stemness characteristics, or immunomodulatory properties. These findings demonstrate the potential of HAMC and cHAMCs as promising candidates for future cell-based therapies, providing a cost-effective solution for large-scale cell production. [Display omitted]
•A novel HA-based microcarrier HAMC as the core material was successfully used for the scalable suspension serum-free culture of hESC-derived MSCs.•The expanded cells maintained their stemness characteristics and immunomodulatory properties.•The newly developed cHAMC showed superior cell attachment and expansion capabilities, leading to higher cell yield.</description><identifier>ISSN: 2590-0064</identifier><identifier>EISSN: 2590-0064</identifier><identifier>DOI: 10.1016/j.mtbio.2023.100662</identifier><identifier>PMID: 37214547</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Bioreactor ; Culture system ; Full Length ; Human embryonic stem cells ; Mesenchymal stem cells ; Microcarrier</subject><ispartof>Materials today bio, 2023-06, Vol.20, p.100662-100662, Article 100662</ispartof><rights>2023 The Authors</rights><rights>2023 The Authors. Published by Elsevier Ltd.</rights><rights>2023 The Authors. Published by Elsevier Ltd. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c476t-b8f05dd2e4b0b360e6f098b622687503884633e83734d749267968e09143982d3</cites><orcidid>0000-0001-9131-6243 ; 0000-0002-6346-4756 ; 0000-0002-5466-0819 ; 0000-0001-9387-9525</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196860/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2590006423001229$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3535,27903,27904,45759,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37214547$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gao, Tingting</creatorcontrib><creatorcontrib>Zhao, Xiyuan</creatorcontrib><creatorcontrib>Hao, Jie</creatorcontrib><creatorcontrib>Tian, Yao</creatorcontrib><creatorcontrib>Ma, Huike</creatorcontrib><creatorcontrib>Liu, Wenjing</creatorcontrib><creatorcontrib>An, Bin</creatorcontrib><creatorcontrib>Sun, Faguo</creatorcontrib><creatorcontrib>Liu, Shasha</creatorcontrib><creatorcontrib>Guo, Baojie</creatorcontrib><creatorcontrib>Niu, Shuaishuai</creatorcontrib><creatorcontrib>Li, Zhongwen</creatorcontrib><creatorcontrib>Wang, Chenxin</creatorcontrib><creatorcontrib>Wang, Yukai</creatorcontrib><creatorcontrib>Feng, Guihai</creatorcontrib><creatorcontrib>Wang, Liu</creatorcontrib><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Wu, Jun</creatorcontrib><creatorcontrib>Guo, Meijin</creatorcontrib><creatorcontrib>Zhou, Qi</creatorcontrib><creatorcontrib>Gu, Qi</creatorcontrib><title>A scalable culture system incorporating microcarrier for specialised mesenchymal stem cells from human embryonic stem cells</title><title>Materials today bio</title><addtitle>Mater Today Bio</addtitle><description>Mesenchymal stromal cells (MSCs) derived from human embryonic stem cells (hESCs) are a desirable cell source for cell therapy owing to their capacity to be produced stably and homogeneously in large quantities. However, a scalable culture system for hPSC-derived MSCs is urgently needed to meet the cell quantity and quality requirements of practical clinical applications. In this study, we developed a new microcarrier with hyaluronic acid (HA) as the core material, which allowed scalable serum-free suspension culture of hESC-derived MSCs (IMRCs). We used optimal microcarriers with a coating collagen concentration of 100 μg/mL or concave-structured surface (cHAMCs) for IMRC amplification in a stirred bioreactor, expanding IMRCs within six days with the highest yield of over one million cells per milliliter. In addition, the harvested cells exhibited high viability, immunomodulatory and regenerative therapeutic promise comparable to monolayer cultured MSCs while showing more increased secretion of extracellular matrix (ECM), particularly collagen-related proteins. In summary, we have established a scalable culture system for hESC-MSCs, providing novel approaches for future cell therapies.
Gu et al. have developed a novel hyaluronic acid microcarrier (HAMC) for scalable suspension serum-free culture of mesenchymal stromal cells derived from human embryonic stem cells (IMRCs) in bioreactor-based systems. The cHAMC, with a concave structure, showed superior cell attachment and expansion capabilities, resulting in higher cell yields without compromising cell proliferation, stemness characteristics, or immunomodulatory properties. These findings demonstrate the potential of HAMC and cHAMCs as promising candidates for future cell-based therapies, providing a cost-effective solution for large-scale cell production. [Display omitted]
•A novel HA-based microcarrier HAMC as the core material was successfully used for the scalable suspension serum-free culture of hESC-derived MSCs.•The expanded cells maintained their stemness characteristics and immunomodulatory properties.•The newly developed cHAMC showed superior cell attachment and expansion capabilities, leading to higher cell yield.</description><subject>Bioreactor</subject><subject>Culture system</subject><subject>Full Length</subject><subject>Human embryonic stem cells</subject><subject>Mesenchymal stem cells</subject><subject>Microcarrier</subject><issn>2590-0064</issn><issn>2590-0064</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kstq3DAUhk1paUKaJygULbuZ6dHFsrwoJYReAoFu2rWQ5OMZDZY1lezAkJevZpyGyaYrSefyHfH_p6reU1hToPLTbh0m6-OaAeMlAlKyV9Ulq1tYlYd4fXa_qK5z3gEAa1oB0L6tLnjDqKhFc1k93pDszGDsgMTNwzQnJPmQJwzEjy6mfUxm8uOGBO9SdCYlj4n0MZG8R-fN4DN2JGDG0W0PwQzk1OtwGDLpUwxkOwczEgw2HeLo3Vn-XfWmN0PG66fzqvr97euv2x-r-5_f725v7ldONHJaWdVD3XUMhQXLJaDsoVVWMiZVUwNXSkjOUfGGi64RLZNNKxVCSwVvFev4VXW3cLtodnqffDDpoKPx-hSIaaNNmrwbUIu6a1XNeqqEFZQ6g8BcobXgTM-kLawvC2s_24Cdw3FKZngBfZkZ_VZv4oMurhWOhEL4-ERI8c-MedLB56MeZsQ4Z80UVVDLWspSypfSIn3OCfvnORSOQKl3-rQG-rgGelmD0vXh_IvPPf9MLwWflwIsoj8UP3V2vviHnU_opqKK_--Av4XNxeI</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Gao, Tingting</creator><creator>Zhao, Xiyuan</creator><creator>Hao, Jie</creator><creator>Tian, Yao</creator><creator>Ma, Huike</creator><creator>Liu, Wenjing</creator><creator>An, Bin</creator><creator>Sun, Faguo</creator><creator>Liu, Shasha</creator><creator>Guo, Baojie</creator><creator>Niu, Shuaishuai</creator><creator>Li, Zhongwen</creator><creator>Wang, Chenxin</creator><creator>Wang, Yukai</creator><creator>Feng, Guihai</creator><creator>Wang, Liu</creator><creator>Li, Wei</creator><creator>Wu, Jun</creator><creator>Guo, Meijin</creator><creator>Zhou, Qi</creator><creator>Gu, Qi</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-9131-6243</orcidid><orcidid>https://orcid.org/0000-0002-6346-4756</orcidid><orcidid>https://orcid.org/0000-0002-5466-0819</orcidid><orcidid>https://orcid.org/0000-0001-9387-9525</orcidid></search><sort><creationdate>20230601</creationdate><title>A scalable culture system incorporating microcarrier for specialised mesenchymal stem cells from human embryonic stem cells</title><author>Gao, Tingting ; Zhao, Xiyuan ; Hao, Jie ; Tian, Yao ; Ma, Huike ; Liu, Wenjing ; An, Bin ; Sun, Faguo ; Liu, Shasha ; Guo, Baojie ; Niu, Shuaishuai ; Li, Zhongwen ; Wang, Chenxin ; Wang, Yukai ; Feng, Guihai ; Wang, Liu ; Li, Wei ; Wu, Jun ; Guo, Meijin ; Zhou, Qi ; Gu, Qi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c476t-b8f05dd2e4b0b360e6f098b622687503884633e83734d749267968e09143982d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Bioreactor</topic><topic>Culture system</topic><topic>Full Length</topic><topic>Human embryonic stem cells</topic><topic>Mesenchymal stem cells</topic><topic>Microcarrier</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gao, Tingting</creatorcontrib><creatorcontrib>Zhao, Xiyuan</creatorcontrib><creatorcontrib>Hao, Jie</creatorcontrib><creatorcontrib>Tian, Yao</creatorcontrib><creatorcontrib>Ma, Huike</creatorcontrib><creatorcontrib>Liu, Wenjing</creatorcontrib><creatorcontrib>An, Bin</creatorcontrib><creatorcontrib>Sun, Faguo</creatorcontrib><creatorcontrib>Liu, Shasha</creatorcontrib><creatorcontrib>Guo, Baojie</creatorcontrib><creatorcontrib>Niu, Shuaishuai</creatorcontrib><creatorcontrib>Li, Zhongwen</creatorcontrib><creatorcontrib>Wang, Chenxin</creatorcontrib><creatorcontrib>Wang, Yukai</creatorcontrib><creatorcontrib>Feng, Guihai</creatorcontrib><creatorcontrib>Wang, Liu</creatorcontrib><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Wu, Jun</creatorcontrib><creatorcontrib>Guo, Meijin</creatorcontrib><creatorcontrib>Zhou, Qi</creatorcontrib><creatorcontrib>Gu, Qi</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Open Access: DOAJ - Directory of Open Access Journals</collection><jtitle>Materials today bio</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gao, Tingting</au><au>Zhao, Xiyuan</au><au>Hao, Jie</au><au>Tian, Yao</au><au>Ma, Huike</au><au>Liu, Wenjing</au><au>An, Bin</au><au>Sun, Faguo</au><au>Liu, Shasha</au><au>Guo, Baojie</au><au>Niu, Shuaishuai</au><au>Li, Zhongwen</au><au>Wang, Chenxin</au><au>Wang, Yukai</au><au>Feng, Guihai</au><au>Wang, Liu</au><au>Li, Wei</au><au>Wu, Jun</au><au>Guo, Meijin</au><au>Zhou, Qi</au><au>Gu, Qi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A scalable culture system incorporating microcarrier for specialised mesenchymal stem cells from human embryonic stem cells</atitle><jtitle>Materials today bio</jtitle><addtitle>Mater Today Bio</addtitle><date>2023-06-01</date><risdate>2023</risdate><volume>20</volume><spage>100662</spage><epage>100662</epage><pages>100662-100662</pages><artnum>100662</artnum><issn>2590-0064</issn><eissn>2590-0064</eissn><abstract>Mesenchymal stromal cells (MSCs) derived from human embryonic stem cells (hESCs) are a desirable cell source for cell therapy owing to their capacity to be produced stably and homogeneously in large quantities. However, a scalable culture system for hPSC-derived MSCs is urgently needed to meet the cell quantity and quality requirements of practical clinical applications. In this study, we developed a new microcarrier with hyaluronic acid (HA) as the core material, which allowed scalable serum-free suspension culture of hESC-derived MSCs (IMRCs). We used optimal microcarriers with a coating collagen concentration of 100 μg/mL or concave-structured surface (cHAMCs) for IMRC amplification in a stirred bioreactor, expanding IMRCs within six days with the highest yield of over one million cells per milliliter. In addition, the harvested cells exhibited high viability, immunomodulatory and regenerative therapeutic promise comparable to monolayer cultured MSCs while showing more increased secretion of extracellular matrix (ECM), particularly collagen-related proteins. In summary, we have established a scalable culture system for hESC-MSCs, providing novel approaches for future cell therapies.
Gu et al. have developed a novel hyaluronic acid microcarrier (HAMC) for scalable suspension serum-free culture of mesenchymal stromal cells derived from human embryonic stem cells (IMRCs) in bioreactor-based systems. The cHAMC, with a concave structure, showed superior cell attachment and expansion capabilities, resulting in higher cell yields without compromising cell proliferation, stemness characteristics, or immunomodulatory properties. These findings demonstrate the potential of HAMC and cHAMCs as promising candidates for future cell-based therapies, providing a cost-effective solution for large-scale cell production. [Display omitted]
•A novel HA-based microcarrier HAMC as the core material was successfully used for the scalable suspension serum-free culture of hESC-derived MSCs.•The expanded cells maintained their stemness characteristics and immunomodulatory properties.•The newly developed cHAMC showed superior cell attachment and expansion capabilities, leading to higher cell yield.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>37214547</pmid><doi>10.1016/j.mtbio.2023.100662</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-9131-6243</orcidid><orcidid>https://orcid.org/0000-0002-6346-4756</orcidid><orcidid>https://orcid.org/0000-0002-5466-0819</orcidid><orcidid>https://orcid.org/0000-0001-9387-9525</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bioreactor Culture system Full Length Human embryonic stem cells Mesenchymal stem cells Microcarrier |
title | A scalable culture system incorporating microcarrier for specialised mesenchymal stem cells from human embryonic stem cells |
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