Transcriptome Analysis of Platelet-Rich Plasma-Treated Osteoarthritic Chondrocyte
As a blood-derived biomaterial, platelet-rich plasma (PRP) has been considered a potential therapy and tried in knee and hip osteoarthritis with beneficial effects as an anti-inflammatory and potent regenerative agent. To better understand the substantial effect of PRP on chondrocytes in an inflamma...
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description | As a blood-derived biomaterial, platelet-rich plasma (PRP) has been considered a potential therapy and tried in knee and hip osteoarthritis with beneficial effects as an anti-inflammatory and potent regenerative agent. To better understand the substantial effect of PRP on chondrocytes in an inflammatory environment, we analyzed the transcriptome profile by RNA sequencing (RNA-seq) after PRP administration in IL-1
-treated osteoarthritic chondrocytes which were isolated from human knee articular cartilage tissue. A total of 24,424 genes were analyzed, and significant changes in expression were observed for 226 genes in the control (CTL) versus IL-1
group and 300 genes in the IL-1
versus IL-1
+PRP group. The Top 20 significantly upregulated and downregulated genes and the major altered genes in nine categories that are closely related to chondrocyte physiology were analyzed, and the expression of several important genes in each category was evaluated by qRT-PCR and western blot analysis. Our study revealed that the PRP, at the gene expression level, has apparent anti-inflammatory, cell proliferative, and regenerative activities in chondrocytes in the presence of IL-1
, which mimic an osteoarthritic environment. Identifying potent molecules that regulate cartilage physiology represents a promising therapeutic approach for suppressing cartilage degeneration, especially that caused by inflammation-induced osteoarthritis. |
doi_str_mv | 10.1155/2024/7680736 |
format | Article |
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-treated osteoarthritic chondrocytes which were isolated from human knee articular cartilage tissue. A total of 24,424 genes were analyzed, and significant changes in expression were observed for 226 genes in the control (CTL) versus IL-1
group and 300 genes in the IL-1
versus IL-1
+PRP group. The Top 20 significantly upregulated and downregulated genes and the major altered genes in nine categories that are closely related to chondrocyte physiology were analyzed, and the expression of several important genes in each category was evaluated by qRT-PCR and western blot analysis. Our study revealed that the PRP, at the gene expression level, has apparent anti-inflammatory, cell proliferative, and regenerative activities in chondrocytes in the presence of IL-1
, which mimic an osteoarthritic environment. Identifying potent molecules that regulate cartilage physiology represents a promising therapeutic approach for suppressing cartilage degeneration, especially that caused by inflammation-induced osteoarthritis.</description><identifier>ISSN: 2314-6133</identifier><identifier>ISSN: 2314-6141</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2024/7680736</identifier><identifier>PMID: 39610694</identifier><language>eng</language><publisher>United States: Hindawi Limited</publisher><subject>Aged ; Antibiotics ; Biological activity ; Blood vessels ; Cartilage ; Cartilage (articular) ; Cartilage diseases ; Cartilage, Articular - metabolism ; Cell Proliferation - drug effects ; Chondrocytes ; Chondrocytes - metabolism ; Degeneration ; Environmental degradation ; Female ; Gene expression ; Gene Expression Profiling ; Gene Expression Regulation - drug effects ; Growth factors ; Homeostasis ; Humans ; Inflammation ; Injury prevention ; Interleukin-1beta - genetics ; Interleukin-1beta - metabolism ; Male ; Middle Aged ; Molecular modelling ; Nerves ; Osteoarthritis ; Osteoarthritis - genetics ; Osteoarthritis - therapy ; Plasma ; Platelet-Rich Plasma - metabolism ; Proteins ; Surgery ; Transcriptome - genetics ; Transcriptomes</subject><ispartof>BioMed research international, 2024, Vol.2024 (1), p.7680736</ispartof><rights>Copyright © 2024 Dae Keun Suh et al.</rights><rights>Copyright © 2024 Dae Keun Suh et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2024 Dae Keun Suh et al. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c262t-467115868c45b50c97d755a2991f47281a0d32265dd94fe094d60068bbeb71aa3</cites><orcidid>0000-0002-6449-8341 ; 0000-0003-0321-1551 ; 0009-0005-4331-7547 ; 0009-0005-9780-0745 ; 0000-0002-3627-8421 ; 0000-0002-0555-5326 ; 0009-0007-4518-4260 ; 0009-0008-4197-051X</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/PMC11604281/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11604281/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,4010,27900,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39610694$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Saeed Mohammadi</contributor><creatorcontrib>Suh, Dae Keun</creatorcontrib><creatorcontrib>Yeo, Woo Jin</creatorcontrib><creatorcontrib>Cheong, Kuhoang</creatorcontrib><creatorcontrib>Heo, Jae-Won</creatorcontrib><creatorcontrib>Kim, Dong Hyeon</creatorcontrib><creatorcontrib>Lee, Soo Mi</creatorcontrib><creatorcontrib>Lee, Yong-Soo</creatorcontrib><creatorcontrib>Suh, Dong Won</creatorcontrib><title>Transcriptome Analysis of Platelet-Rich Plasma-Treated Osteoarthritic Chondrocyte</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>As a blood-derived biomaterial, platelet-rich plasma (PRP) has been considered a potential therapy and tried in knee and hip osteoarthritis with beneficial effects as an anti-inflammatory and potent regenerative agent. To better understand the substantial effect of PRP on chondrocytes in an inflammatory environment, we analyzed the transcriptome profile by RNA sequencing (RNA-seq) after PRP administration in IL-1
-treated osteoarthritic chondrocytes which were isolated from human knee articular cartilage tissue. A total of 24,424 genes were analyzed, and significant changes in expression were observed for 226 genes in the control (CTL) versus IL-1
group and 300 genes in the IL-1
versus IL-1
+PRP group. The Top 20 significantly upregulated and downregulated genes and the major altered genes in nine categories that are closely related to chondrocyte physiology were analyzed, and the expression of several important genes in each category was evaluated by qRT-PCR and western blot analysis. Our study revealed that the PRP, at the gene expression level, has apparent anti-inflammatory, cell proliferative, and regenerative activities in chondrocytes in the presence of IL-1
, which mimic an osteoarthritic environment. Identifying potent molecules that regulate cartilage physiology represents a promising therapeutic approach for suppressing cartilage degeneration, especially that caused by inflammation-induced osteoarthritis.</description><subject>Aged</subject><subject>Antibiotics</subject><subject>Biological activity</subject><subject>Blood vessels</subject><subject>Cartilage</subject><subject>Cartilage (articular)</subject><subject>Cartilage diseases</subject><subject>Cartilage, Articular - metabolism</subject><subject>Cell Proliferation - drug effects</subject><subject>Chondrocytes</subject><subject>Chondrocytes - metabolism</subject><subject>Degeneration</subject><subject>Environmental degradation</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Growth factors</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Injury prevention</subject><subject>Interleukin-1beta - 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metabolism</topic><topic>Cell Proliferation - drug effects</topic><topic>Chondrocytes</topic><topic>Chondrocytes - metabolism</topic><topic>Degeneration</topic><topic>Environmental degradation</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Growth factors</topic><topic>Homeostasis</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Injury prevention</topic><topic>Interleukin-1beta - genetics</topic><topic>Interleukin-1beta - metabolism</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Molecular modelling</topic><topic>Nerves</topic><topic>Osteoarthritis</topic><topic>Osteoarthritis - genetics</topic><topic>Osteoarthritis - therapy</topic><topic>Plasma</topic><topic>Platelet-Rich Plasma - metabolism</topic><topic>Proteins</topic><topic>Surgery</topic><topic>Transcriptome - genetics</topic><topic>Transcriptomes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suh, Dae Keun</creatorcontrib><creatorcontrib>Yeo, Woo Jin</creatorcontrib><creatorcontrib>Cheong, Kuhoang</creatorcontrib><creatorcontrib>Heo, Jae-Won</creatorcontrib><creatorcontrib>Kim, Dong Hyeon</creatorcontrib><creatorcontrib>Lee, Soo Mi</creatorcontrib><creatorcontrib>Lee, Yong-Soo</creatorcontrib><creatorcontrib>Suh, Dong Won</creatorcontrib><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>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Middle East & Africa Database</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>AIDS and Cancer Research Abstracts</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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</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 China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BioMed research international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suh, Dae Keun</au><au>Yeo, Woo Jin</au><au>Cheong, Kuhoang</au><au>Heo, Jae-Won</au><au>Kim, Dong Hyeon</au><au>Lee, Soo Mi</au><au>Lee, Yong-Soo</au><au>Suh, Dong Won</au><au>Saeed Mohammadi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transcriptome Analysis of Platelet-Rich Plasma-Treated Osteoarthritic Chondrocyte</atitle><jtitle>BioMed research international</jtitle><addtitle>Biomed Res Int</addtitle><date>2024</date><risdate>2024</risdate><volume>2024</volume><issue>1</issue><spage>7680736</spage><pages>7680736-</pages><issn>2314-6133</issn><issn>2314-6141</issn><eissn>2314-6141</eissn><abstract>As a blood-derived biomaterial, platelet-rich plasma (PRP) has been considered a potential therapy and tried in knee and hip osteoarthritis with beneficial effects as an anti-inflammatory and potent regenerative agent. To better understand the substantial effect of PRP on chondrocytes in an inflammatory environment, we analyzed the transcriptome profile by RNA sequencing (RNA-seq) after PRP administration in IL-1
-treated osteoarthritic chondrocytes which were isolated from human knee articular cartilage tissue. A total of 24,424 genes were analyzed, and significant changes in expression were observed for 226 genes in the control (CTL) versus IL-1
group and 300 genes in the IL-1
versus IL-1
+PRP group. The Top 20 significantly upregulated and downregulated genes and the major altered genes in nine categories that are closely related to chondrocyte physiology were analyzed, and the expression of several important genes in each category was evaluated by qRT-PCR and western blot analysis. Our study revealed that the PRP, at the gene expression level, has apparent anti-inflammatory, cell proliferative, and regenerative activities in chondrocytes in the presence of IL-1
, which mimic an osteoarthritic environment. Identifying potent molecules that regulate cartilage physiology represents a promising therapeutic approach for suppressing cartilage degeneration, especially that caused by inflammation-induced osteoarthritis.</abstract><cop>United States</cop><pub>Hindawi Limited</pub><pmid>39610694</pmid><doi>10.1155/2024/7680736</doi><orcidid>https://orcid.org/0000-0002-6449-8341</orcidid><orcidid>https://orcid.org/0000-0003-0321-1551</orcidid><orcidid>https://orcid.org/0009-0005-4331-7547</orcidid><orcidid>https://orcid.org/0009-0005-9780-0745</orcidid><orcidid>https://orcid.org/0000-0002-3627-8421</orcidid><orcidid>https://orcid.org/0000-0002-0555-5326</orcidid><orcidid>https://orcid.org/0009-0007-4518-4260</orcidid><orcidid>https://orcid.org/0009-0008-4197-051X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aged Antibiotics Biological activity Blood vessels Cartilage Cartilage (articular) Cartilage diseases Cartilage, Articular - metabolism Cell Proliferation - drug effects Chondrocytes Chondrocytes - metabolism Degeneration Environmental degradation Female Gene expression Gene Expression Profiling Gene Expression Regulation - drug effects Growth factors Homeostasis Humans Inflammation Injury prevention Interleukin-1beta - genetics Interleukin-1beta - metabolism Male Middle Aged Molecular modelling Nerves Osteoarthritis Osteoarthritis - genetics Osteoarthritis - therapy Plasma Platelet-Rich Plasma - metabolism Proteins Surgery Transcriptome - genetics Transcriptomes |
title | Transcriptome Analysis of Platelet-Rich Plasma-Treated Osteoarthritic Chondrocyte |
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