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We are analyzing https://link.springer.com/article/10.1186/ar2080.

Title:
Fibroblast activation protein is expressed by rheumatoid myofibroblast-like synoviocytes | Arthritis Research & Therapy
Description:
Fibroblast activation protein (FAP), as described so far, is a type II cell surface serine protease expressed by fibroblastic cells in areas of active tissue remodelling such as tumour stroma or healing wounds. We investigated the expression of FAP by fibroblast-like synoviocytes (FLSs) and compared the synovial expression pattern in rheumatoid arthritis (RA) and osteoarthritis (OA) patients. Synovial tissue from diseased joints of 20 patients, 10 patients with refractory RA and 10 patients with end-stage OA, was collected during routine surgery. As a result, FLSs from intensively inflamed synovial tissues of refractory RA expressed FAP at high density. Moreover, FAP expression was co-localised with matrix metalloproteinases (MMP-1 and MMP-13) and CD44 splice variants v3 and v7/8 known to play a major role in the concert of extracellular matrix degradation. The pattern of signals appeared to constitute a characteristic feature of FLSs involved in rheumatoid arthritic joint-destructive processes. These FAP-expressing FLSs with a phenotype of smooth muscle actin-positive myofibroblasts were located in the lining layer of the synovium and differ distinctly from Thy-1-expressing and non-proliferating fibroblasts of the articular matrix. The intensity of FAP-specific staining in synovial tissue from patients with RA was found to be different when compared with end-stage OA. Because expression of FAP by RA FLSs has not been described before, the findings of this study highlight a novel element in cartilage and bone destruction of arthritic joints. Moreover, the specific expression pattern qualifies FAP as a therapeutic target for inhibiting the destructive potential of fibroblast-like synovial cells.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • Science

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We don’t know how the website earns money.

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Keywords {🔍}

fap, synovial, expression, article, pubmed, arthritis, rheumatoid, patients, google, scholar, mmp, cas, tissue, activation, samples, fibroblast, protein, fibroblasts, matrix, figure, flss, cell, analysis, cells, pcr, staining, cancer, gene, lining, markers, antihuman, joints, central, authors, fibroblastlike, layer, human, sma, synoviocytes, rheum, research, expressed, surface, refractory, synovium, activity, ecm, cdv, germany, original,

Topics {✒️}

cell-surface antigen-restricted activation article download pdf augments antibody-mediated cytotoxicity anti-fibroblast-directed therapy quantitative reverse transcription-pcr transforming growth factor-beta irrelevant isotype-matched igg mouse anti-human cd44v3 epithelium-mesenchyme interactions contributing reverse transcription-pcr analysis dakocytomation envision doublestain-kit minor low-grade uptake humanised anti-fap antibody tissue-tek oct medium central cellular mediator metastatic fap-positive cancer goat anti-human mmp-1 t-cell immune response fibroblast activation protein mock-transfected ht1080 cells fibroblast-mediated cartilage degradation fap-transfected ht1080 cells biotinylated secondary antibody smooth muscle actin collagen-induced arthritis including dpp iv/cd26 smooth-muscle differentiation german research society fap-expressing myofibroblastic cells antibody-abc complex anti-human cd90 privacy choices/manage cookies enzymatic activity resulted rheumatoid arthritis show real-time pcr synovial cell type authors’ original file distinct fibroblast population biotin blocking system cell surface glycoprotein fap-specific targeting results rheumatoid factor-positive full access normal tissue repair article number r171 anti-human cd44v3 cell surface-bound cell-surface glycoproteins antigen-positive cells serine prolyl oligopeptidases

Questions {❓}

  • Muller-Ladner U, Gay S: MMPs and rheumatoid synovial fibroblasts: Siamese twins in joint destruction?
  • Passive responders or transformed aggressors?
  • Sedo A, Duke-Cohan JS, Balaziova E, Sedova LR: Dipeptidyl peptidase IV activity and/or structure homologs: contributing factors in the pathogenesis of rheumatoid arthritis?

Schema {🗺️}

WebPage:
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         headline:Fibroblast activation protein is expressed by rheumatoid myofibroblast-like synoviocytes
         description:Fibroblast activation protein (FAP), as described so far, is a type II cell surface serine protease expressed by fibroblastic cells in areas of active tissue remodelling such as tumour stroma or healing wounds. We investigated the expression of FAP by fibroblast-like synoviocytes (FLSs) and compared the synovial expression pattern in rheumatoid arthritis (RA) and osteoarthritis (OA) patients. Synovial tissue from diseased joints of 20 patients, 10 patients with refractory RA and 10 patients with end-stage OA, was collected during routine surgery. As a result, FLSs from intensively inflamed synovial tissues of refractory RA expressed FAP at high density. Moreover, FAP expression was co-localised with matrix metalloproteinases (MMP-1 and MMP-13) and CD44 splice variants v3 and v7/8 known to play a major role in the concert of extracellular matrix degradation. The pattern of signals appeared to constitute a characteristic feature of FLSs involved in rheumatoid arthritic joint-destructive processes. These FAP-expressing FLSs with a phenotype of smooth muscle actin-positive myofibroblasts were located in the lining layer of the synovium and differ distinctly from Thy-1-expressing and non-proliferating fibroblasts of the articular matrix. The intensity of FAP-specific staining in synovial tissue from patients with RA was found to be different when compared with end-stage OA. Because expression of FAP by RA FLSs has not been described before, the findings of this study highlight a novel element in cartilage and bone destruction of arthritic joints. Moreover, the specific expression pattern qualifies FAP as a therapeutic target for inhibiting the destructive potential of fibroblast-like synovial cells.
         datePublished:2006-11-14T00:00:00Z
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            Rheumatology
            Orthopedics
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      headline:Fibroblast activation protein is expressed by rheumatoid myofibroblast-like synoviocytes
      description:Fibroblast activation protein (FAP), as described so far, is a type II cell surface serine protease expressed by fibroblastic cells in areas of active tissue remodelling such as tumour stroma or healing wounds. We investigated the expression of FAP by fibroblast-like synoviocytes (FLSs) and compared the synovial expression pattern in rheumatoid arthritis (RA) and osteoarthritis (OA) patients. Synovial tissue from diseased joints of 20 patients, 10 patients with refractory RA and 10 patients with end-stage OA, was collected during routine surgery. As a result, FLSs from intensively inflamed synovial tissues of refractory RA expressed FAP at high density. Moreover, FAP expression was co-localised with matrix metalloproteinases (MMP-1 and MMP-13) and CD44 splice variants v3 and v7/8 known to play a major role in the concert of extracellular matrix degradation. The pattern of signals appeared to constitute a characteristic feature of FLSs involved in rheumatoid arthritic joint-destructive processes. These FAP-expressing FLSs with a phenotype of smooth muscle actin-positive myofibroblasts were located in the lining layer of the synovium and differ distinctly from Thy-1-expressing and non-proliferating fibroblasts of the articular matrix. The intensity of FAP-specific staining in synovial tissue from patients with RA was found to be different when compared with end-stage OA. Because expression of FAP by RA FLSs has not been described before, the findings of this study highlight a novel element in cartilage and bone destruction of arthritic joints. Moreover, the specific expression pattern qualifies FAP as a therapeutic target for inhibiting the destructive potential of fibroblast-like synovial cells.
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      dateModified:2006-11-14T00:00:00Z
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         Rheumatoid Arthritis
         Synovial Tissue
         Synovial Sample
         Fibroblast Activation Protein
         Rheumatoid Synovium
         Rheumatology
         Orthopedics
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                     type:PostalAddress
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                     type:PostalAddress
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                     type:PostalAddress
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            type:Person
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            affiliation:
                  name:University of Giessen and Kerckhoff-Clinic
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            name:Universität des Saarlandes, Kirrbergstrasse
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               name:Department of Internal Medicine and Rheumatology, University of Giessen and Kerckhoff-Clinic, Bad Nauheim, Germany
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            name:UniversitätsSpital Zürich
            address:
               name:Oncology Department, UniversitätsSpital Zürich, Zürich, Switzerland
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Oncology Department, UniversitätsSpital Zürich, Zürich, Switzerland
      name:Med. Department I, Universität des Saarlandes, Kirrbergstrasse, Homburg/Saar, Germany
      name:Oncology Department, UniversitätsSpital Zürich, Zürich, Switzerland
      name:Oncology Department, UniversitätsSpital Zürich, Zürich, Switzerland
      name:Oncology Department, UniversitätsSpital Zürich, Zürich, Switzerland
      name:Department of Internal Medicine and Rheumatology, University of Giessen and Kerckhoff-Clinic, Bad Nauheim, Germany
      name:Med. Department I, Universität des Saarlandes, Kirrbergstrasse, Homburg/Saar, Germany
      name:Oncology Department, UniversitätsSpital Zürich, Zürich, Switzerland
      name:Orthopedic Department, Universität des Saarlandes, Kirrbergstrasse, Homburg/Saar, Germany
      name:Orthopedic Clinic, Westpfalz-Klinikum, Kusel, Germany
      name:Department of Internal Medicine and Rheumatology, University of Giessen and Kerckhoff-Clinic, Bad Nauheim, Germany
      name:Oncology Department, UniversitätsSpital Zürich, Zürich, Switzerland

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