Design of novel functionalized collagen-chitosan-MBG scaffolds for enhancing osteoblast differentiation in BMSCs
Collagen and chitosan are two different kinds of natural biodegradable polymers commonly used in the regeneration of bone defects. Mesoporous bioactive glass (MBG) is a type of favorable bone filler which can effectively constitute an enlarged microenvironment to facilitate an exchange of important...
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Veröffentlicht in: | Biomedical materials (Bristol) 2021-11, Vol.16 (6), p.65028 |
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creator | Gao, Kai Wang, Xiaoyan Wang, Zhonghua He, Lijiao Lin, Jiayu Bai, Zhenzu Jiang, Kai Huang, Shan Zheng, Weijia Liu, Long |
description | Collagen and chitosan are two different kinds of natural biodegradable polymers commonly used in the regeneration of bone defects. Mesoporous bioactive glass (MBG) is a type of favorable bone filler which can effectively constitute an enlarged microenvironment to facilitate an exchange of important factors between the cells and scaffolds. Here we prepared a collagen-chitosan-MBG (C-C-MBG) scaffold which displayed significantly increased proliferation, differentiation and mineralization in bone mesenchymal stem cells (BMSCs). Additionally, we found that the scaffold can stimulate extra-cellular signal regulated kinase 1/2 (Erk1/2) activated Runx2 pathway, which is the predominant signaling pathway involved in osteoblast differentiation. Consistently, we observed that the scaffold can markedly enhance the expression of
(
), and
, which are important osteoblastic marker genes implicated in the process of osteoblast differentiation. Therefore, we conclude that the composite scaffold can significantly promote the differentiation of BMSCs into osteoblasts by activating Erk1/2-Runx2 pathway. Our finding thereby implies that the C-C-MBG scaffold can possibly act as a potential biomaterial in the bone regeneration. |
doi_str_mv | 10.1088/1748-605X/ac3146 |
format | Article |
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(
), and
, which are important osteoblastic marker genes implicated in the process of osteoblast differentiation. Therefore, we conclude that the composite scaffold can significantly promote the differentiation of BMSCs into osteoblasts by activating Erk1/2-Runx2 pathway. Our finding thereby implies that the C-C-MBG scaffold can possibly act as a potential biomaterial in the bone regeneration.</description><identifier>ISSN: 1748-6041</identifier><identifier>EISSN: 1748-605X</identifier><identifier>DOI: 10.1088/1748-605X/ac3146</identifier><identifier>PMID: 34670204</identifier><identifier>CODEN: BMBUCS</identifier><language>eng</language><publisher>England: IOP Publishing</publisher><subject>Cell Differentiation ; Chitosan ; collagen ; Collagen - metabolism ; Erk1/2-Runx2 ; Glass ; MBG ; Mesenchymal Stem Cells ; Osteoblasts ; Osteogenesis ; Porosity ; Tissue Scaffolds</subject><ispartof>Biomedical materials (Bristol), 2021-11, Vol.16 (6), p.65028</ispartof><rights>2021 IOP Publishing Ltd</rights><rights>2021 IOP Publishing Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-d6d0370780fc93e27c5f3a1b0cabb7c64456f8a5173c78d15209b3ff66c0de923</citedby><cites>FETCH-LOGICAL-c368t-d6d0370780fc93e27c5f3a1b0cabb7c64456f8a5173c78d15209b3ff66c0de923</cites><orcidid>0000-0003-4649-5232</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://iopscience.iop.org/article/10.1088/1748-605X/ac3146/pdf$$EPDF$$P50$$Giop$$H</linktopdf><link.rule.ids>314,780,784,27924,27925,53846,53893</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34670204$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gao, Kai</creatorcontrib><creatorcontrib>Wang, Xiaoyan</creatorcontrib><creatorcontrib>Wang, Zhonghua</creatorcontrib><creatorcontrib>He, Lijiao</creatorcontrib><creatorcontrib>Lin, Jiayu</creatorcontrib><creatorcontrib>Bai, Zhenzu</creatorcontrib><creatorcontrib>Jiang, Kai</creatorcontrib><creatorcontrib>Huang, Shan</creatorcontrib><creatorcontrib>Zheng, Weijia</creatorcontrib><creatorcontrib>Liu, Long</creatorcontrib><title>Design of novel functionalized collagen-chitosan-MBG scaffolds for enhancing osteoblast differentiation in BMSCs</title><title>Biomedical materials (Bristol)</title><addtitle>BMM</addtitle><addtitle>Biomed. Mater</addtitle><description>Collagen and chitosan are two different kinds of natural biodegradable polymers commonly used in the regeneration of bone defects. Mesoporous bioactive glass (MBG) is a type of favorable bone filler which can effectively constitute an enlarged microenvironment to facilitate an exchange of important factors between the cells and scaffolds. Here we prepared a collagen-chitosan-MBG (C-C-MBG) scaffold which displayed significantly increased proliferation, differentiation and mineralization in bone mesenchymal stem cells (BMSCs). Additionally, we found that the scaffold can stimulate extra-cellular signal regulated kinase 1/2 (Erk1/2) activated Runx2 pathway, which is the predominant signaling pathway involved in osteoblast differentiation. Consistently, we observed that the scaffold can markedly enhance the expression of
(
), and
, which are important osteoblastic marker genes implicated in the process of osteoblast differentiation. Therefore, we conclude that the composite scaffold can significantly promote the differentiation of BMSCs into osteoblasts by activating Erk1/2-Runx2 pathway. Our finding thereby implies that the C-C-MBG scaffold can possibly act as a potential biomaterial in the bone regeneration.</description><subject>Cell Differentiation</subject><subject>Chitosan</subject><subject>collagen</subject><subject>Collagen - metabolism</subject><subject>Erk1/2-Runx2</subject><subject>Glass</subject><subject>MBG</subject><subject>Mesenchymal Stem Cells</subject><subject>Osteoblasts</subject><subject>Osteogenesis</subject><subject>Porosity</subject><subject>Tissue Scaffolds</subject><issn>1748-6041</issn><issn>1748-605X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD1v2zAQhomgRey42TsF3Nqhio-iSFFj7TYfQIwMbYFsBMUPh4ZEKqIUIP31keHUU5HpDofnfYF7EPpM4JKAEEtSFiLjwB6WSlNS8BM0P54-HPeCzNBZSjsAVjFanaIZLXgJORRz1P2wyW8Djg6H-Gwb7MagBx-Davxfa7COTaO2NmT60Q8xqZBtVtc4aeVcbEzCLvbYhkcVtA9bHNNgY92oNGDjnbO9DYNX-zrsA15tfq3TJ_TRqSbZ87e5QH-ufv5e32R399e36-93maZcDJnhBmgJpQCnK2rzUjNHFalBq7ouNS8Kxp1QjJRUl8IQlkNVU-c412BsldMF-nro7fr4NNo0yNYnbadvgo1jkjkTrCA5FdWEwgHVfUypt052vW9V_yIJyL1nuRcp91LlwfMUuXhrH-vWmmPgn9gJ-HYAfOzkLo79JDS91_flP3jdtpJwySVwBrmQnXH0FbyNlT8</recordid><startdate>20211101</startdate><enddate>20211101</enddate><creator>Gao, Kai</creator><creator>Wang, Xiaoyan</creator><creator>Wang, Zhonghua</creator><creator>He, Lijiao</creator><creator>Lin, Jiayu</creator><creator>Bai, Zhenzu</creator><creator>Jiang, Kai</creator><creator>Huang, Shan</creator><creator>Zheng, Weijia</creator><creator>Liu, Long</creator><general>IOP Publishing</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>7X8</scope><orcidid>https://orcid.org/0000-0003-4649-5232</orcidid></search><sort><creationdate>20211101</creationdate><title>Design of novel functionalized collagen-chitosan-MBG scaffolds for enhancing osteoblast differentiation in BMSCs</title><author>Gao, Kai ; Wang, Xiaoyan ; Wang, Zhonghua ; He, Lijiao ; Lin, Jiayu ; Bai, Zhenzu ; Jiang, Kai ; Huang, Shan ; Zheng, Weijia ; Liu, Long</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-d6d0370780fc93e27c5f3a1b0cabb7c64456f8a5173c78d15209b3ff66c0de923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Cell Differentiation</topic><topic>Chitosan</topic><topic>collagen</topic><topic>Collagen - metabolism</topic><topic>Erk1/2-Runx2</topic><topic>Glass</topic><topic>MBG</topic><topic>Mesenchymal Stem Cells</topic><topic>Osteoblasts</topic><topic>Osteogenesis</topic><topic>Porosity</topic><topic>Tissue Scaffolds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gao, Kai</creatorcontrib><creatorcontrib>Wang, Xiaoyan</creatorcontrib><creatorcontrib>Wang, Zhonghua</creatorcontrib><creatorcontrib>He, Lijiao</creatorcontrib><creatorcontrib>Lin, Jiayu</creatorcontrib><creatorcontrib>Bai, Zhenzu</creatorcontrib><creatorcontrib>Jiang, Kai</creatorcontrib><creatorcontrib>Huang, Shan</creatorcontrib><creatorcontrib>Zheng, Weijia</creatorcontrib><creatorcontrib>Liu, Long</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biomedical materials (Bristol)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gao, Kai</au><au>Wang, Xiaoyan</au><au>Wang, Zhonghua</au><au>He, Lijiao</au><au>Lin, Jiayu</au><au>Bai, Zhenzu</au><au>Jiang, Kai</au><au>Huang, Shan</au><au>Zheng, Weijia</au><au>Liu, Long</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design of novel functionalized collagen-chitosan-MBG scaffolds for enhancing osteoblast differentiation in BMSCs</atitle><jtitle>Biomedical materials (Bristol)</jtitle><stitle>BMM</stitle><addtitle>Biomed. Mater</addtitle><date>2021-11-01</date><risdate>2021</risdate><volume>16</volume><issue>6</issue><spage>65028</spage><pages>65028-</pages><issn>1748-6041</issn><eissn>1748-605X</eissn><coden>BMBUCS</coden><abstract>Collagen and chitosan are two different kinds of natural biodegradable polymers commonly used in the regeneration of bone defects. Mesoporous bioactive glass (MBG) is a type of favorable bone filler which can effectively constitute an enlarged microenvironment to facilitate an exchange of important factors between the cells and scaffolds. Here we prepared a collagen-chitosan-MBG (C-C-MBG) scaffold which displayed significantly increased proliferation, differentiation and mineralization in bone mesenchymal stem cells (BMSCs). Additionally, we found that the scaffold can stimulate extra-cellular signal regulated kinase 1/2 (Erk1/2) activated Runx2 pathway, which is the predominant signaling pathway involved in osteoblast differentiation. Consistently, we observed that the scaffold can markedly enhance the expression of
(
), and
, which are important osteoblastic marker genes implicated in the process of osteoblast differentiation. Therefore, we conclude that the composite scaffold can significantly promote the differentiation of BMSCs into osteoblasts by activating Erk1/2-Runx2 pathway. Our finding thereby implies that the C-C-MBG scaffold can possibly act as a potential biomaterial in the bone regeneration.</abstract><cop>England</cop><pub>IOP Publishing</pub><pmid>34670204</pmid><doi>10.1088/1748-605X/ac3146</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-4649-5232</orcidid></addata></record> |
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subjects | Cell Differentiation Chitosan collagen Collagen - metabolism Erk1/2-Runx2 Glass MBG Mesenchymal Stem Cells Osteoblasts Osteogenesis Porosity Tissue Scaffolds |
title | Design of novel functionalized collagen-chitosan-MBG scaffolds for enhancing osteoblast differentiation in BMSCs |
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