Expression of β-1,4-galactosyltransferase Ⅰ in a surgically-induced rat model of knee osteoarthritic synovitis

Background There are few reports of a biological role for glycosyltransferases in the infiltration of osteoarthritic synovitis. The aim of this research was to investigate the expression and cellular location of β-1,4-galactosyltransferase Ⅰ (β-1,4-GaIT-Ⅰ) in a surgically-induced rat model of knee o...

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Veröffentlicht in:Chinese medical journal 2010-11, Vol.123 (21), p.3067-3073
Hauptverfasser: Wang, You-Hua, Ni, Xiao-Hui, Xu, Da-Wei, Cai, Hao, Wang, Hai-Rong, Sun, Fa-Rui, Shen, Ai-Guo
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container_end_page 3073
container_issue 21
container_start_page 3067
container_title Chinese medical journal
container_volume 123
creator Wang, You-Hua
Ni, Xiao-Hui
Xu, Da-Wei
Cai, Hao
Wang, Hai-Rong
Sun, Fa-Rui
Shen, Ai-Guo
description Background There are few reports of a biological role for glycosyltransferases in the infiltration of osteoarthritic synovitis. The aim of this research was to investigate the expression and cellular location of β-1,4-galactosyltransferase Ⅰ (β-1,4-GaIT-Ⅰ) in a surgically-induced rat model of knee osteoarthritis (OA), and explore the role of β-1,4-GalT-Ⅰ in the pathogenesis of OA.Methods Male Sprague-Dawley rats were randomly divided into three groups: OA group, sham group and normal group. The model of OA was established in the right knees of rats by anterior cruciate ligament transaction (ACLT) with partial medial meniscectomy. Fibroblast-like synoviocytes (FLSs) obtained from normal rat synovial tissue were cultured.The expression of β-1,4-GalT-Ⅰ mRNA in the synovial tissue, articular cartilage and FLSs treated with tumor necrosis factor-α (TNF-α) were assayed by real-time PCR. Western-blotting and immunohistochemisty were used to observe the expression of β-1,4-GalT-Ⅰ at the protein level. Double immunofluorescent staining was used to define the location of the β-1,4-GalT-Ⅰ with macrophage-like synoviocytes, FLSs, neutrophils, and TNF-α in the OA synovium. The alteration of TNF-α in FLSs which were treated with lipopolysaccharide (LPS) and β-1,4-GalT-Ⅰ-Ab were detected by enzyme-linked immunosorbent assay (ELISA).Results The mRNA and protein expression of β-1,4-GalT-Ⅰ increased in synovial tissue of the OA group compared with the normal and sham groups at two and four weeks after the surgery, however, no significant difference appeared in the articular cartilage. Immunohistochemistry also indicated that the β-1,4-GalT-Ⅰ expression in OA synovium at four weeks after surgery increased sharply compared with the control group. β-1,4-GalT-Ⅰ co-localized with macrophage-like synoviocytes, FLSa, neutrophils and TNF-α in rat OA synovitis. Moreover, in vitro β-1,4-GalT-Ⅰ mRNA in FLSs was affected in a dose- and time-dependent manner in response to TNF-α stimulation. ELISA revealed that the expression of TNF-α was attenuated in FLSs in vitro when treated with anti β-1,4-GalT-Ⅰ antibody.Conclusion β-1,4-GalT-Ⅰ may play an important role in the inflammation process of rat OA synovial tissue which would provide the foundation for further researching into the concrete mechanism of β-1,4-GalT-Ⅰ in OA synovitis.
doi_str_mv 10.3760/cma.j.issn.0366-6999.2010.21.021
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The aim of this research was to investigate the expression and cellular location of β-1,4-galactosyltransferase Ⅰ (β-1,4-GaIT-Ⅰ) in a surgically-induced rat model of knee osteoarthritis (OA), and explore the role of β-1,4-GalT-Ⅰ in the pathogenesis of OA.Methods Male Sprague-Dawley rats were randomly divided into three groups: OA group, sham group and normal group. The model of OA was established in the right knees of rats by anterior cruciate ligament transaction (ACLT) with partial medial meniscectomy. Fibroblast-like synoviocytes (FLSs) obtained from normal rat synovial tissue were cultured.The expression of β-1,4-GalT-Ⅰ mRNA in the synovial tissue, articular cartilage and FLSs treated with tumor necrosis factor-α (TNF-α) were assayed by real-time PCR. Western-blotting and immunohistochemisty were used to observe the expression of β-1,4-GalT-Ⅰ at the protein level. Double immunofluorescent staining was used to define the location of the β-1,4-GalT-Ⅰ with macrophage-like synoviocytes, FLSs, neutrophils, and TNF-α in the OA synovium. The alteration of TNF-α in FLSs which were treated with lipopolysaccharide (LPS) and β-1,4-GalT-Ⅰ-Ab were detected by enzyme-linked immunosorbent assay (ELISA).Results The mRNA and protein expression of β-1,4-GalT-Ⅰ increased in synovial tissue of the OA group compared with the normal and sham groups at two and four weeks after the surgery, however, no significant difference appeared in the articular cartilage. Immunohistochemistry also indicated that the β-1,4-GalT-Ⅰ expression in OA synovium at four weeks after surgery increased sharply compared with the control group. β-1,4-GalT-Ⅰ co-localized with macrophage-like synoviocytes, FLSa, neutrophils and TNF-α in rat OA synovitis. Moreover, in vitro β-1,4-GalT-Ⅰ mRNA in FLSs was affected in a dose- and time-dependent manner in response to TNF-α stimulation. ELISA revealed that the expression of TNF-α was attenuated in FLSs in vitro when treated with anti β-1,4-GalT-Ⅰ antibody.Conclusion β-1,4-GalT-Ⅰ may play an important role in the inflammation process of rat OA synovial tissue which would provide the foundation for further researching into the concrete mechanism of β-1,4-GalT-Ⅰ in OA synovitis.</description><identifier>ISSN: 0366-6999</identifier><identifier>EISSN: 2542-5641</identifier><identifier>DOI: 10.3760/cma.j.issn.0366-6999.2010.21.021</identifier><identifier>PMID: 21162957</identifier><language>eng</language><publisher>China: Department of Orthopaedics, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, China%Department of Immunology, Medical College, Nantong University,Nantong, Jiangsu 226001, China</publisher><subject>Animals ; Blotting, Western ; Cells, Cultured ; Enzyme-Linked Immunosorbent Assay ; Galactosyltransferases - genetics ; Galactosyltransferases - metabolism ; Immunohistochemistry ; Knee Joint - enzymology ; Knee Joint - pathology ; Knee Joint - surgery ; Male ; Osteoarthritis, Knee - enzymology ; Osteoarthritis, Knee - genetics ; Osteoarthritis, Knee - pathology ; Polymerase Chain Reaction ; Rats ; Rats, Sprague-Dawley ; Synovial Membrane - enzymology ; Synovitis - enzymology ; Synovitis - etiology ; 半乳糖 ; 大鼠模型 ; 滑膜炎 ; 膝关节 ; 转移酶 ; 酶联免疫吸附试验 ; 骨性关节炎</subject><ispartof>Chinese medical journal, 2010-11, Vol.123 (21), p.3067-3073</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/85656X/85656X.jpg</thumbnail><link.rule.ids>314,776,780,860,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21162957$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, You-Hua</creatorcontrib><creatorcontrib>Ni, Xiao-Hui</creatorcontrib><creatorcontrib>Xu, Da-Wei</creatorcontrib><creatorcontrib>Cai, Hao</creatorcontrib><creatorcontrib>Wang, Hai-Rong</creatorcontrib><creatorcontrib>Sun, Fa-Rui</creatorcontrib><creatorcontrib>Shen, Ai-Guo</creatorcontrib><title>Expression of β-1,4-galactosyltransferase Ⅰ in a surgically-induced rat model of knee osteoarthritic synovitis</title><title>Chinese medical journal</title><addtitle>Chinese Medical Journal</addtitle><description>Background There are few reports of a biological role for glycosyltransferases in the infiltration of osteoarthritic synovitis. The aim of this research was to investigate the expression and cellular location of β-1,4-galactosyltransferase Ⅰ (β-1,4-GaIT-Ⅰ) in a surgically-induced rat model of knee osteoarthritis (OA), and explore the role of β-1,4-GalT-Ⅰ in the pathogenesis of OA.Methods Male Sprague-Dawley rats were randomly divided into three groups: OA group, sham group and normal group. The model of OA was established in the right knees of rats by anterior cruciate ligament transaction (ACLT) with partial medial meniscectomy. Fibroblast-like synoviocytes (FLSs) obtained from normal rat synovial tissue were cultured.The expression of β-1,4-GalT-Ⅰ mRNA in the synovial tissue, articular cartilage and FLSs treated with tumor necrosis factor-α (TNF-α) were assayed by real-time PCR. Western-blotting and immunohistochemisty were used to observe the expression of β-1,4-GalT-Ⅰ at the protein level. Double immunofluorescent staining was used to define the location of the β-1,4-GalT-Ⅰ with macrophage-like synoviocytes, FLSs, neutrophils, and TNF-α in the OA synovium. The alteration of TNF-α in FLSs which were treated with lipopolysaccharide (LPS) and β-1,4-GalT-Ⅰ-Ab were detected by enzyme-linked immunosorbent assay (ELISA).Results The mRNA and protein expression of β-1,4-GalT-Ⅰ increased in synovial tissue of the OA group compared with the normal and sham groups at two and four weeks after the surgery, however, no significant difference appeared in the articular cartilage. Immunohistochemistry also indicated that the β-1,4-GalT-Ⅰ expression in OA synovium at four weeks after surgery increased sharply compared with the control group. β-1,4-GalT-Ⅰ co-localized with macrophage-like synoviocytes, FLSa, neutrophils and TNF-α in rat OA synovitis. Moreover, in vitro β-1,4-GalT-Ⅰ mRNA in FLSs was affected in a dose- and time-dependent manner in response to TNF-α stimulation. ELISA revealed that the expression of TNF-α was attenuated in FLSs in vitro when treated with anti β-1,4-GalT-Ⅰ antibody.Conclusion β-1,4-GalT-Ⅰ may play an important role in the inflammation process of rat OA synovial tissue which would provide the foundation for further researching into the concrete mechanism of β-1,4-GalT-Ⅰ in OA synovitis.</description><subject>Animals</subject><subject>Blotting, Western</subject><subject>Cells, Cultured</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Galactosyltransferases - genetics</subject><subject>Galactosyltransferases - metabolism</subject><subject>Immunohistochemistry</subject><subject>Knee Joint - enzymology</subject><subject>Knee Joint - pathology</subject><subject>Knee Joint - surgery</subject><subject>Male</subject><subject>Osteoarthritis, Knee - enzymology</subject><subject>Osteoarthritis, Knee - genetics</subject><subject>Osteoarthritis, Knee - pathology</subject><subject>Polymerase Chain Reaction</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Synovial Membrane - enzymology</subject><subject>Synovitis - enzymology</subject><subject>Synovitis - etiology</subject><subject>半乳糖</subject><subject>大鼠模型</subject><subject>滑膜炎</subject><subject>膝关节</subject><subject>转移酶</subject><subject>酶联免疫吸附试验</subject><subject>骨性关节炎</subject><issn>0366-6999</issn><issn>2542-5641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo90M1u1DAQB3ALgei28ArI4gA9NMHfdo6oKlCpEhc4RxPb2fU2sXftBFjuvAfPwIPwEDwJWW1BGmlGmp_mLw1Cl5TUXCvyxo5Qb-tQSqwJV6pSTdPUjCxrRmvC6CO0YlKwSipBH6PVf3OGzkvZEsKk1OopOmOUKtZIvUL7m2-77EsJKeLU49-_KnolqjUMYKdUDsOUIZbeZyge__nxE4eIAZc5r4OFYThUIbrZeoczTHhMzg_HK_fRe5zK5BPkaZPDFCwuh5i-LFN5hp70MBT__KFfoM_vbj5df6juPr6_vX57V1mmzFR1WmklpLWu61VvDRVGc0e4F9QaofvOEHBguOJCOQq6aVTXyE502jitvOMX6NXp7leIPcR1u01zjkti-31jx-3xa-xYC3x9gruc9rMvUzuGYv0wQPRpLq2hRgnemKN88SDnbvSu3eUwQj60_965gJcnYDcprvdhSe3A3vdh8C2XhikpDP8L4-eJ1Q</recordid><startdate>20101105</startdate><enddate>20101105</enddate><creator>Wang, You-Hua</creator><creator>Ni, Xiao-Hui</creator><creator>Xu, Da-Wei</creator><creator>Cai, Hao</creator><creator>Wang, Hai-Rong</creator><creator>Sun, Fa-Rui</creator><creator>Shen, Ai-Guo</creator><general>Department of Orthopaedics, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, China%Department of Immunology, Medical College, Nantong University,Nantong, Jiangsu 226001, China</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W94</scope><scope>WU4</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20101105</creationdate><title>Expression of β-1,4-galactosyltransferase Ⅰ in a surgically-induced rat model of knee osteoarthritic synovitis</title><author>Wang, You-Hua ; 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The aim of this research was to investigate the expression and cellular location of β-1,4-galactosyltransferase Ⅰ (β-1,4-GaIT-Ⅰ) in a surgically-induced rat model of knee osteoarthritis (OA), and explore the role of β-1,4-GalT-Ⅰ in the pathogenesis of OA.Methods Male Sprague-Dawley rats were randomly divided into three groups: OA group, sham group and normal group. The model of OA was established in the right knees of rats by anterior cruciate ligament transaction (ACLT) with partial medial meniscectomy. Fibroblast-like synoviocytes (FLSs) obtained from normal rat synovial tissue were cultured.The expression of β-1,4-GalT-Ⅰ mRNA in the synovial tissue, articular cartilage and FLSs treated with tumor necrosis factor-α (TNF-α) were assayed by real-time PCR. Western-blotting and immunohistochemisty were used to observe the expression of β-1,4-GalT-Ⅰ at the protein level. Double immunofluorescent staining was used to define the location of the β-1,4-GalT-Ⅰ with macrophage-like synoviocytes, FLSs, neutrophils, and TNF-α in the OA synovium. The alteration of TNF-α in FLSs which were treated with lipopolysaccharide (LPS) and β-1,4-GalT-Ⅰ-Ab were detected by enzyme-linked immunosorbent assay (ELISA).Results The mRNA and protein expression of β-1,4-GalT-Ⅰ increased in synovial tissue of the OA group compared with the normal and sham groups at two and four weeks after the surgery, however, no significant difference appeared in the articular cartilage. Immunohistochemistry also indicated that the β-1,4-GalT-Ⅰ expression in OA synovium at four weeks after surgery increased sharply compared with the control group. β-1,4-GalT-Ⅰ co-localized with macrophage-like synoviocytes, FLSa, neutrophils and TNF-α in rat OA synovitis. Moreover, in vitro β-1,4-GalT-Ⅰ mRNA in FLSs was affected in a dose- and time-dependent manner in response to TNF-α stimulation. ELISA revealed that the expression of TNF-α was attenuated in FLSs in vitro when treated with anti β-1,4-GalT-Ⅰ antibody.Conclusion β-1,4-GalT-Ⅰ may play an important role in the inflammation process of rat OA synovial tissue which would provide the foundation for further researching into the concrete mechanism of β-1,4-GalT-Ⅰ in OA synovitis.</abstract><cop>China</cop><pub>Department of Orthopaedics, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, China%Department of Immunology, Medical College, Nantong University,Nantong, Jiangsu 226001, China</pub><pmid>21162957</pmid><doi>10.3760/cma.j.issn.0366-6999.2010.21.021</doi><tpages>7</tpages></addata></record>
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subjects Animals
Blotting, Western
Cells, Cultured
Enzyme-Linked Immunosorbent Assay
Galactosyltransferases - genetics
Galactosyltransferases - metabolism
Immunohistochemistry
Knee Joint - enzymology
Knee Joint - pathology
Knee Joint - surgery
Male
Osteoarthritis, Knee - enzymology
Osteoarthritis, Knee - genetics
Osteoarthritis, Knee - pathology
Polymerase Chain Reaction
Rats
Rats, Sprague-Dawley
Synovial Membrane - enzymology
Synovitis - enzymology
Synovitis - etiology
半乳糖
大鼠模型
滑膜炎
膝关节
转移酶
酶联免疫吸附试验
骨性关节炎
title Expression of β-1,4-galactosyltransferase Ⅰ in a surgically-induced rat model of knee osteoarthritic synovitis
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