Enhancement of mesenchymal stem cells’ chondrogenic potential by type II collagen-based bioscaffolds
Background Osteoarthritis (OA) is a common degenerative chronic disease accounting for physical pain, tissue stiffness and mobility restriction. Current therapeutic approaches fail to prevent the progression of the disease considering the limited knowledge on OA pathobiology. During OA progression,...
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creator | Piperigkou, Zoi Bainantzou, Dimitra Makri, Nadia Papachristou, Eleni Mantsou, Aglaia Choli-Papadopoulou, Theodora Theocharis, Achilleas D. Karamanos, Nikos K. |
description | Background
Osteoarthritis (OA) is a common degenerative chronic disease accounting for physical pain, tissue stiffness and mobility restriction. Current therapeutic approaches fail to prevent the progression of the disease considering the limited knowledge on OA pathobiology. During OA progression, the extracellular matrix (ECM) of the cartilage is aberrantly remodeled by chondrocytes. Chondrocytes, being the main cell population of the cartilage, participate in cartilage regeneration process. To this end, modern tissue engineering strategies involve the recruitment of mesenchymal stem cells (MSCs) due to their regenerative capacity as to promote chondrocyte self-regeneration.
Methods and results
In the present study, we evaluated the role of type II collagen, as the main matrix macromolecule in the cartilage matrix, to promote chondrogenic differentiation in two MSC in vitro culture systems. The chondrogenic differentiation of human Wharton’s jelly- and dental pulp-derived MSCs was investigated over a 24-day culture period on type II collagen coating to improve the binding affinity of MSCs. Functional assays, demonstrated that type II collagen promoted chondrogenic differentiation in both MSCs tested, which was confirmed through gene and protein analysis of major chondrogenic markers.
Conclusions
Our data support that type II collagen contributes as a natural bioscaffold enhancing chondrogenesis in both MSC models, thus enhancing the commitment of MSC-based therapeutic approaches in regenerative medicine to target OA and bring therapy closer to the clinical use. |
doi_str_mv | 10.1007/s11033-023-08461-x |
format | Article |
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Osteoarthritis (OA) is a common degenerative chronic disease accounting for physical pain, tissue stiffness and mobility restriction. Current therapeutic approaches fail to prevent the progression of the disease considering the limited knowledge on OA pathobiology. During OA progression, the extracellular matrix (ECM) of the cartilage is aberrantly remodeled by chondrocytes. Chondrocytes, being the main cell population of the cartilage, participate in cartilage regeneration process. To this end, modern tissue engineering strategies involve the recruitment of mesenchymal stem cells (MSCs) due to their regenerative capacity as to promote chondrocyte self-regeneration.
Methods and results
In the present study, we evaluated the role of type II collagen, as the main matrix macromolecule in the cartilage matrix, to promote chondrogenic differentiation in two MSC in vitro culture systems. The chondrogenic differentiation of human Wharton’s jelly- and dental pulp-derived MSCs was investigated over a 24-day culture period on type II collagen coating to improve the binding affinity of MSCs. Functional assays, demonstrated that type II collagen promoted chondrogenic differentiation in both MSCs tested, which was confirmed through gene and protein analysis of major chondrogenic markers.
Conclusions
Our data support that type II collagen contributes as a natural bioscaffold enhancing chondrogenesis in both MSC models, thus enhancing the commitment of MSC-based therapeutic approaches in regenerative medicine to target OA and bring therapy closer to the clinical use.</description><identifier>ISSN: 0301-4851</identifier><identifier>EISSN: 1573-4978</identifier><identifier>DOI: 10.1007/s11033-023-08461-x</identifier><identifier>PMID: 37118382</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Animal Anatomy ; Animal Biochemistry ; Biomedical and Life Sciences ; Cartilage ; Cartilage diseases ; Cell culture ; Cell Culture Techniques ; Cell- and Tissue-Based Therapy ; Chondrocytes ; Chondrocytes - cytology ; Chondrocytes - metabolism ; Chondrogenesis ; Collagen ; Collagen Type II ; Dental pulp ; Dental Pulp - cytology ; Extracellular matrix ; Histology ; Humans ; Life Sciences ; Matrix Metalloproteinases - metabolism ; Mesenchymal stem cells ; Mesenchymal Stem Cells - cytology ; Morphology ; Original ; Original Article ; Osteoarthritis ; Osteoarthritis - therapy ; Primary Cell Culture - methods ; Regenerative medicine ; Stem cells ; Tissue engineering ; Tissue Inhibitor of Metalloproteinases - metabolism ; Umbilical Cord - cytology</subject><ispartof>Molecular biology reports, 2023-06, Vol.50 (6), p.5125-5135</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c426t-454c64cb26b91c3f9332d49a6b95aeada73468e645ca29dd24a3242d3f2b7b533</cites><orcidid>0000-0002-7459-5807 ; 0000-0003-3618-0288 ; 0000-0002-0472-5389 ; 0000-0001-8611-2297</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11033-023-08461-x$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11033-023-08461-x$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37118382$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Piperigkou, Zoi</creatorcontrib><creatorcontrib>Bainantzou, Dimitra</creatorcontrib><creatorcontrib>Makri, Nadia</creatorcontrib><creatorcontrib>Papachristou, Eleni</creatorcontrib><creatorcontrib>Mantsou, Aglaia</creatorcontrib><creatorcontrib>Choli-Papadopoulou, Theodora</creatorcontrib><creatorcontrib>Theocharis, Achilleas D.</creatorcontrib><creatorcontrib>Karamanos, Nikos K.</creatorcontrib><title>Enhancement of mesenchymal stem cells’ chondrogenic potential by type II collagen-based bioscaffolds</title><title>Molecular biology reports</title><addtitle>Mol Biol Rep</addtitle><addtitle>Mol Biol Rep</addtitle><description>Background
Osteoarthritis (OA) is a common degenerative chronic disease accounting for physical pain, tissue stiffness and mobility restriction. Current therapeutic approaches fail to prevent the progression of the disease considering the limited knowledge on OA pathobiology. During OA progression, the extracellular matrix (ECM) of the cartilage is aberrantly remodeled by chondrocytes. Chondrocytes, being the main cell population of the cartilage, participate in cartilage regeneration process. To this end, modern tissue engineering strategies involve the recruitment of mesenchymal stem cells (MSCs) due to their regenerative capacity as to promote chondrocyte self-regeneration.
Methods and results
In the present study, we evaluated the role of type II collagen, as the main matrix macromolecule in the cartilage matrix, to promote chondrogenic differentiation in two MSC in vitro culture systems. The chondrogenic differentiation of human Wharton’s jelly- and dental pulp-derived MSCs was investigated over a 24-day culture period on type II collagen coating to improve the binding affinity of MSCs. Functional assays, demonstrated that type II collagen promoted chondrogenic differentiation in both MSCs tested, which was confirmed through gene and protein analysis of major chondrogenic markers.
Conclusions
Our data support that type II collagen contributes as a natural bioscaffold enhancing chondrogenesis in both MSC models, thus enhancing the commitment of MSC-based therapeutic approaches in regenerative medicine to target OA and bring therapy closer to the clinical use.</description><subject>Animal Anatomy</subject><subject>Animal Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Cartilage</subject><subject>Cartilage diseases</subject><subject>Cell culture</subject><subject>Cell Culture Techniques</subject><subject>Cell- and Tissue-Based Therapy</subject><subject>Chondrocytes</subject><subject>Chondrocytes - cytology</subject><subject>Chondrocytes - metabolism</subject><subject>Chondrogenesis</subject><subject>Collagen</subject><subject>Collagen Type II</subject><subject>Dental pulp</subject><subject>Dental Pulp - cytology</subject><subject>Extracellular matrix</subject><subject>Histology</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Matrix Metalloproteinases - metabolism</subject><subject>Mesenchymal stem cells</subject><subject>Mesenchymal Stem Cells - cytology</subject><subject>Morphology</subject><subject>Original</subject><subject>Original Article</subject><subject>Osteoarthritis</subject><subject>Osteoarthritis - therapy</subject><subject>Primary Cell Culture - methods</subject><subject>Regenerative medicine</subject><subject>Stem cells</subject><subject>Tissue engineering</subject><subject>Tissue Inhibitor of Metalloproteinases - metabolism</subject><subject>Umbilical Cord - cytology</subject><issn>0301-4851</issn><issn>1573-4978</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kU1OHDEQha0oURggF8gCWWLDpoN_2-5VFCEgIyGxCWvLbVfPNOq2B7snYnZcg-txEgxDSGCRhWVZ76tXVX4IfaXkGyVEHWdKCecVYeVoUdPq9gOaUal4JRqlP6IZ4YRWQku6g3ZzviaECKrkZ7TDFaWaazZD3WlY2uBghDDh2OERMgS33Ix2wHmCETsYhvxwd4_dMgaf4gJC7_AqTqWgL1C7wdNmBXg-xy4Ogy161doMHrd9zM52XRx83kefOjtk-PJy76Grs9NfJz-ri8vz-cmPi8oJVk-VkMLVwrWsbhvqeNdwzrxobHlKC9ZbxUWtoRbSWdZ4z4TlTDDPO9aqVnK-h75vfVfrdgTvypDJDmaV-tGmjYm2N2-V0C_NIv42lDDSMK2Kw9GLQ4o3a8iTGfv89Ak2QFxnwzRRDZWiIQU9fIdex3UKZb9CUS1lLTUrFNtSLsWcE3Sv01BinnI02xxNydE852huS9HBv3u8lvwJrgB8C-QihQWkv73_Y_sIMyGrww</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Piperigkou, Zoi</creator><creator>Bainantzou, Dimitra</creator><creator>Makri, Nadia</creator><creator>Papachristou, Eleni</creator><creator>Mantsou, Aglaia</creator><creator>Choli-Papadopoulou, Theodora</creator><creator>Theocharis, Achilleas D.</creator><creator>Karamanos, Nikos K.</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>C6C</scope><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>3V.</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7459-5807</orcidid><orcidid>https://orcid.org/0000-0003-3618-0288</orcidid><orcidid>https://orcid.org/0000-0002-0472-5389</orcidid><orcidid>https://orcid.org/0000-0001-8611-2297</orcidid></search><sort><creationdate>20230601</creationdate><title>Enhancement of mesenchymal stem cells’ chondrogenic potential by type II collagen-based bioscaffolds</title><author>Piperigkou, Zoi ; Bainantzou, Dimitra ; Makri, Nadia ; Papachristou, Eleni ; Mantsou, Aglaia ; Choli-Papadopoulou, Theodora ; Theocharis, Achilleas D. ; Karamanos, Nikos K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-454c64cb26b91c3f9332d49a6b95aeada73468e645ca29dd24a3242d3f2b7b533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animal Anatomy</topic><topic>Animal Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Cartilage</topic><topic>Cartilage diseases</topic><topic>Cell culture</topic><topic>Cell Culture Techniques</topic><topic>Cell- and Tissue-Based Therapy</topic><topic>Chondrocytes</topic><topic>Chondrocytes - cytology</topic><topic>Chondrocytes - metabolism</topic><topic>Chondrogenesis</topic><topic>Collagen</topic><topic>Collagen Type II</topic><topic>Dental pulp</topic><topic>Dental Pulp - cytology</topic><topic>Extracellular matrix</topic><topic>Histology</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Matrix Metalloproteinases - metabolism</topic><topic>Mesenchymal stem cells</topic><topic>Mesenchymal Stem Cells - cytology</topic><topic>Morphology</topic><topic>Original</topic><topic>Original Article</topic><topic>Osteoarthritis</topic><topic>Osteoarthritis - therapy</topic><topic>Primary Cell Culture - methods</topic><topic>Regenerative medicine</topic><topic>Stem cells</topic><topic>Tissue engineering</topic><topic>Tissue Inhibitor of Metalloproteinases - metabolism</topic><topic>Umbilical Cord - cytology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Piperigkou, Zoi</creatorcontrib><creatorcontrib>Bainantzou, Dimitra</creatorcontrib><creatorcontrib>Makri, Nadia</creatorcontrib><creatorcontrib>Papachristou, Eleni</creatorcontrib><creatorcontrib>Mantsou, Aglaia</creatorcontrib><creatorcontrib>Choli-Papadopoulou, Theodora</creatorcontrib><creatorcontrib>Theocharis, Achilleas D.</creatorcontrib><creatorcontrib>Karamanos, Nikos K.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular biology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Piperigkou, Zoi</au><au>Bainantzou, Dimitra</au><au>Makri, Nadia</au><au>Papachristou, Eleni</au><au>Mantsou, Aglaia</au><au>Choli-Papadopoulou, Theodora</au><au>Theocharis, Achilleas D.</au><au>Karamanos, Nikos K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enhancement of mesenchymal stem cells’ chondrogenic potential by type II collagen-based bioscaffolds</atitle><jtitle>Molecular biology reports</jtitle><stitle>Mol Biol Rep</stitle><addtitle>Mol Biol Rep</addtitle><date>2023-06-01</date><risdate>2023</risdate><volume>50</volume><issue>6</issue><spage>5125</spage><epage>5135</epage><pages>5125-5135</pages><issn>0301-4851</issn><eissn>1573-4978</eissn><abstract>Background
Osteoarthritis (OA) is a common degenerative chronic disease accounting for physical pain, tissue stiffness and mobility restriction. Current therapeutic approaches fail to prevent the progression of the disease considering the limited knowledge on OA pathobiology. During OA progression, the extracellular matrix (ECM) of the cartilage is aberrantly remodeled by chondrocytes. Chondrocytes, being the main cell population of the cartilage, participate in cartilage regeneration process. To this end, modern tissue engineering strategies involve the recruitment of mesenchymal stem cells (MSCs) due to their regenerative capacity as to promote chondrocyte self-regeneration.
Methods and results
In the present study, we evaluated the role of type II collagen, as the main matrix macromolecule in the cartilage matrix, to promote chondrogenic differentiation in two MSC in vitro culture systems. The chondrogenic differentiation of human Wharton’s jelly- and dental pulp-derived MSCs was investigated over a 24-day culture period on type II collagen coating to improve the binding affinity of MSCs. Functional assays, demonstrated that type II collagen promoted chondrogenic differentiation in both MSCs tested, which was confirmed through gene and protein analysis of major chondrogenic markers.
Conclusions
Our data support that type II collagen contributes as a natural bioscaffold enhancing chondrogenesis in both MSC models, thus enhancing the commitment of MSC-based therapeutic approaches in regenerative medicine to target OA and bring therapy closer to the clinical use.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>37118382</pmid><doi>10.1007/s11033-023-08461-x</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-7459-5807</orcidid><orcidid>https://orcid.org/0000-0003-3618-0288</orcidid><orcidid>https://orcid.org/0000-0002-0472-5389</orcidid><orcidid>https://orcid.org/0000-0001-8611-2297</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animal Anatomy Animal Biochemistry Biomedical and Life Sciences Cartilage Cartilage diseases Cell culture Cell Culture Techniques Cell- and Tissue-Based Therapy Chondrocytes Chondrocytes - cytology Chondrocytes - metabolism Chondrogenesis Collagen Collagen Type II Dental pulp Dental Pulp - cytology Extracellular matrix Histology Humans Life Sciences Matrix Metalloproteinases - metabolism Mesenchymal stem cells Mesenchymal Stem Cells - cytology Morphology Original Original Article Osteoarthritis Osteoarthritis - therapy Primary Cell Culture - methods Regenerative medicine Stem cells Tissue engineering Tissue Inhibitor of Metalloproteinases - metabolism Umbilical Cord - cytology |
title | Enhancement of mesenchymal stem cells’ chondrogenic potential by type II collagen-based bioscaffolds |
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