Effect of CD44 on differentiation of human amniotic mesenchymal stem cells into chondrocytes via Smad and ERK signaling pathways
CD44 antigen (CD44) is a transmembrane protein found in cell adhesion molecules and is involved in the regulation of various physiological processes in cells. It was hypothesized that CD44 directly affected the chondrogenic differentiation of human amniotic mesenchymal stem cells (hAMSCs). In the pr...
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Veröffentlicht in: | Molecular medicine reports 2020-06, Vol.21 (6), p.2357-2366 |
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description | CD44 antigen (CD44) is a transmembrane protein found in cell adhesion molecules and is involved in the regulation of various physiological processes in cells. It was hypothesized that CD44 directly affected the chondrogenic differentiation of human amniotic mesenchymal stem cells (hAMSCs). In the present study, the expression of chondrocyte‑associated factors was detected in the absence and presence of the antibody blocker anti‑CD44 antibody during the chondrogenic differentiation of hAMSCs. Following inhibition of CD44 expression, the transcriptional levels of chondrocyte‑associated genes SRY‑box transcription factor 9, aggrecan and collagen type II α 1 chain, as well as the production of chondrocyte markers type II collagen and aggrecan were significantly decreased in hAMSCs. Further investigation indicated that there was no significant change in total ERK1/2 expression following inhibition of CD44 expression; however, phosphorylated (p)‑ERK1/2 expression was decreased. The expression of p‑Smad2/3 was also upregulated following CD44 inhibition. These data indicated that CD44 may affect the differentiation of hAMSCs into chondrocytes by regulating the Smad2/3 and ERK1/2 signaling pathway. |
doi_str_mv | 10.3892/mmr.2020.11044 |
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It was hypothesized that CD44 directly affected the chondrogenic differentiation of human amniotic mesenchymal stem cells (hAMSCs). In the present study, the expression of chondrocyte‑associated factors was detected in the absence and presence of the antibody blocker anti‑CD44 antibody during the chondrogenic differentiation of hAMSCs. Following inhibition of CD44 expression, the transcriptional levels of chondrocyte‑associated genes SRY‑box transcription factor 9, aggrecan and collagen type II α 1 chain, as well as the production of chondrocyte markers type II collagen and aggrecan were significantly decreased in hAMSCs. Further investigation indicated that there was no significant change in total ERK1/2 expression following inhibition of CD44 expression; however, phosphorylated (p)‑ERK1/2 expression was decreased. The expression of p‑Smad2/3 was also upregulated following CD44 inhibition. These data indicated that CD44 may affect the differentiation of hAMSCs into chondrocytes by regulating the Smad2/3 and ERK1/2 signaling pathway.</description><identifier>ISSN: 1791-2997</identifier><identifier>EISSN: 1791-3004</identifier><identifier>DOI: 10.3892/mmr.2020.11044</identifier><identifier>PMID: 32236637</identifier><language>eng</language><publisher>Greece: Spandidos Publications</publisher><subject>Aggrecan ; Aggrecans - metabolism ; Amnion - metabolism ; Antibodies ; Antigens ; Apoptosis ; Arthritis ; Cartilage ; CD44 antigen ; Cell adhesion molecules ; Cell Differentiation - drug effects ; Chondrocytes ; Chondrocytes - metabolism ; Chondrogenesis ; Chondrogenesis - drug effects ; Collagen ; Collagen (type II) ; Collagen Type II - metabolism ; Drug dosages ; Extracellular signal-regulated kinase ; Flow cytometry ; Genes ; Growth factors ; Humans ; Hyaluronan Receptors - genetics ; Hyaluronan Receptors - metabolism ; Kinases ; MAP Kinase Signaling System ; Mesenchymal stem cells ; Mesenchymal Stem Cells - metabolism ; Phosphorylation ; Proteins ; Signal transduction ; Signal Transduction - drug effects ; Smad protein ; Smad2 protein ; Smad2 Protein - metabolism ; Smad3 Protein - metabolism ; Stem cells ; Transcription (Genetics)</subject><ispartof>Molecular medicine reports, 2020-06, Vol.21 (6), p.2357-2366</ispartof><rights>COPYRIGHT 2020 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2020</rights><rights>Copyright: © Xu et al. 2020</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c485t-d256b71f6e81d06c40fc947387546a8834604e5d3664614b1a4f7a7309a4d0843</citedby><cites>FETCH-LOGICAL-c485t-d256b71f6e81d06c40fc947387546a8834604e5d3664614b1a4f7a7309a4d0843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32236637$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Yan</creatorcontrib><creatorcontrib>Wang, Yi-Qing</creatorcontrib><creatorcontrib>Wang, Ai-Tong</creatorcontrib><creatorcontrib>Yu, Chang-Yin</creatorcontrib><creatorcontrib>Luo, Yi</creatorcontrib><creatorcontrib>Liu, Ru-Ming</creatorcontrib><creatorcontrib>Zhao, Yu-Jie</creatorcontrib><creatorcontrib>Xiao, Jian-Hui</creatorcontrib><title>Effect of CD44 on differentiation of human amniotic mesenchymal stem cells into chondrocytes via Smad and ERK signaling pathways</title><title>Molecular medicine reports</title><addtitle>Mol Med Rep</addtitle><description>CD44 antigen (CD44) is a transmembrane protein found in cell adhesion molecules and is involved in the regulation of various physiological processes in cells. It was hypothesized that CD44 directly affected the chondrogenic differentiation of human amniotic mesenchymal stem cells (hAMSCs). In the present study, the expression of chondrocyte‑associated factors was detected in the absence and presence of the antibody blocker anti‑CD44 antibody during the chondrogenic differentiation of hAMSCs. Following inhibition of CD44 expression, the transcriptional levels of chondrocyte‑associated genes SRY‑box transcription factor 9, aggrecan and collagen type II α 1 chain, as well as the production of chondrocyte markers type II collagen and aggrecan were significantly decreased in hAMSCs. Further investigation indicated that there was no significant change in total ERK1/2 expression following inhibition of CD44 expression; however, phosphorylated (p)‑ERK1/2 expression was decreased. The expression of p‑Smad2/3 was also upregulated following CD44 inhibition. These data indicated that CD44 may affect the differentiation of hAMSCs into chondrocytes by regulating the Smad2/3 and ERK1/2 signaling pathway.</description><subject>Aggrecan</subject><subject>Aggrecans - metabolism</subject><subject>Amnion - metabolism</subject><subject>Antibodies</subject><subject>Antigens</subject><subject>Apoptosis</subject><subject>Arthritis</subject><subject>Cartilage</subject><subject>CD44 antigen</subject><subject>Cell adhesion molecules</subject><subject>Cell Differentiation - drug effects</subject><subject>Chondrocytes</subject><subject>Chondrocytes - metabolism</subject><subject>Chondrogenesis</subject><subject>Chondrogenesis - drug effects</subject><subject>Collagen</subject><subject>Collagen (type II)</subject><subject>Collagen Type II - metabolism</subject><subject>Drug dosages</subject><subject>Extracellular signal-regulated kinase</subject><subject>Flow cytometry</subject><subject>Genes</subject><subject>Growth factors</subject><subject>Humans</subject><subject>Hyaluronan Receptors - genetics</subject><subject>Hyaluronan Receptors - metabolism</subject><subject>Kinases</subject><subject>MAP Kinase Signaling System</subject><subject>Mesenchymal stem cells</subject><subject>Mesenchymal Stem Cells - metabolism</subject><subject>Phosphorylation</subject><subject>Proteins</subject><subject>Signal transduction</subject><subject>Signal Transduction - drug effects</subject><subject>Smad protein</subject><subject>Smad2 protein</subject><subject>Smad2 Protein - metabolism</subject><subject>Smad3 Protein - metabolism</subject><subject>Stem cells</subject><subject>Transcription (Genetics)</subject><issn>1791-2997</issn><issn>1791-3004</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><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>eNptksmPFCEYxStG4yx69WhIvHjplh3qYjLp6VHjJCYuZ0KzdDMpoIWqMX3zT5fSdlwy4QB8_L5HHryue4bgksgev4qxLDHEcIkQpPRBd4pEjxYEQvrwuMZ9L066s1pvIOQMs_5xd0IwJpwTcdp9X3vvzAiyB6tLSkFOwIZWKi6NQY-h7dvRboo6AR1TyGMwILrqktkdoh5AHV0Exg1DBSGNGZhdTrZkcxhdBbdBg09RW6CTBeuP70EN26SHkLZgr8fdN32oT7pHXg_VPT3O592Xq_Xn1dvF9Yc371YX1wtDJRsXFjO-EchzJ5GF3FDoTU8FkYJRrqUklEPqmG22KEd0gzT1QgsCe00tlJScd69_6e6nTXTWNH9FD2pfQtTloLIO6t-TFHZqm2-VQJJhiZvAy6NAyV8nV0cVQ52N6-TyVBUmkgkoSM8a-uI_9CZPpRlvFIWI9YQh_Ifa6sGpkHxu95pZVF1wzET7UD5rLe-h2rAuBpOT86HV72swJddanL_ziKCaM6NaZtScGfUzM63h-d8vc4f_Dgn5AQkJu8w</recordid><startdate>20200601</startdate><enddate>20200601</enddate><creator>Xu, Yan</creator><creator>Wang, Yi-Qing</creator><creator>Wang, Ai-Tong</creator><creator>Yu, Chang-Yin</creator><creator>Luo, Yi</creator><creator>Liu, Ru-Ming</creator><creator>Zhao, Yu-Jie</creator><creator>Xiao, Jian-Hui</creator><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><general>D.A. 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metabolism</topic><topic>Amnion - metabolism</topic><topic>Antibodies</topic><topic>Antigens</topic><topic>Apoptosis</topic><topic>Arthritis</topic><topic>Cartilage</topic><topic>CD44 antigen</topic><topic>Cell adhesion molecules</topic><topic>Cell Differentiation - drug effects</topic><topic>Chondrocytes</topic><topic>Chondrocytes - metabolism</topic><topic>Chondrogenesis</topic><topic>Chondrogenesis - drug effects</topic><topic>Collagen</topic><topic>Collagen (type II)</topic><topic>Collagen Type II - metabolism</topic><topic>Drug dosages</topic><topic>Extracellular signal-regulated kinase</topic><topic>Flow cytometry</topic><topic>Genes</topic><topic>Growth factors</topic><topic>Humans</topic><topic>Hyaluronan Receptors - genetics</topic><topic>Hyaluronan Receptors - metabolism</topic><topic>Kinases</topic><topic>MAP Kinase Signaling System</topic><topic>Mesenchymal stem cells</topic><topic>Mesenchymal Stem Cells - metabolism</topic><topic>Phosphorylation</topic><topic>Proteins</topic><topic>Signal transduction</topic><topic>Signal Transduction - drug effects</topic><topic>Smad protein</topic><topic>Smad2 protein</topic><topic>Smad2 Protein - metabolism</topic><topic>Smad3 Protein - metabolism</topic><topic>Stem cells</topic><topic>Transcription (Genetics)</topic><toplevel>online_resources</toplevel><creatorcontrib>Xu, Yan</creatorcontrib><creatorcontrib>Wang, Yi-Qing</creatorcontrib><creatorcontrib>Wang, Ai-Tong</creatorcontrib><creatorcontrib>Yu, Chang-Yin</creatorcontrib><creatorcontrib>Luo, Yi</creatorcontrib><creatorcontrib>Liu, Ru-Ming</creatorcontrib><creatorcontrib>Zhao, Yu-Jie</creatorcontrib><creatorcontrib>Xiao, Jian-Hui</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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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>British Nursing Database</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>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>Biological Science 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>Molecular medicine reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Yan</au><au>Wang, Yi-Qing</au><au>Wang, Ai-Tong</au><au>Yu, Chang-Yin</au><au>Luo, Yi</au><au>Liu, Ru-Ming</au><au>Zhao, Yu-Jie</au><au>Xiao, Jian-Hui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of CD44 on differentiation of human amniotic mesenchymal stem cells into chondrocytes via Smad and ERK signaling pathways</atitle><jtitle>Molecular medicine reports</jtitle><addtitle>Mol Med Rep</addtitle><date>2020-06-01</date><risdate>2020</risdate><volume>21</volume><issue>6</issue><spage>2357</spage><epage>2366</epage><pages>2357-2366</pages><issn>1791-2997</issn><eissn>1791-3004</eissn><abstract>CD44 antigen (CD44) is a transmembrane protein found in cell adhesion molecules and is involved in the regulation of various physiological processes in cells. It was hypothesized that CD44 directly affected the chondrogenic differentiation of human amniotic mesenchymal stem cells (hAMSCs). In the present study, the expression of chondrocyte‑associated factors was detected in the absence and presence of the antibody blocker anti‑CD44 antibody during the chondrogenic differentiation of hAMSCs. Following inhibition of CD44 expression, the transcriptional levels of chondrocyte‑associated genes SRY‑box transcription factor 9, aggrecan and collagen type II α 1 chain, as well as the production of chondrocyte markers type II collagen and aggrecan were significantly decreased in hAMSCs. Further investigation indicated that there was no significant change in total ERK1/2 expression following inhibition of CD44 expression; however, phosphorylated (p)‑ERK1/2 expression was decreased. The expression of p‑Smad2/3 was also upregulated following CD44 inhibition. These data indicated that CD44 may affect the differentiation of hAMSCs into chondrocytes by regulating the Smad2/3 and ERK1/2 signaling pathway.</abstract><cop>Greece</cop><pub>Spandidos Publications</pub><pmid>32236637</pmid><doi>10.3892/mmr.2020.11044</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aggrecan Aggrecans - metabolism Amnion - metabolism Antibodies Antigens Apoptosis Arthritis Cartilage CD44 antigen Cell adhesion molecules Cell Differentiation - drug effects Chondrocytes Chondrocytes - metabolism Chondrogenesis Chondrogenesis - drug effects Collagen Collagen (type II) Collagen Type II - metabolism Drug dosages Extracellular signal-regulated kinase Flow cytometry Genes Growth factors Humans Hyaluronan Receptors - genetics Hyaluronan Receptors - metabolism Kinases MAP Kinase Signaling System Mesenchymal stem cells Mesenchymal Stem Cells - metabolism Phosphorylation Proteins Signal transduction Signal Transduction - drug effects Smad protein Smad2 protein Smad2 Protein - metabolism Smad3 Protein - metabolism Stem cells Transcription (Genetics) |
title | Effect of CD44 on differentiation of human amniotic mesenchymal stem cells into chondrocytes via Smad and ERK signaling pathways |
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