TDAG8, TRPV1, and ASIC3 involved in establishing hyperalgesic priming in experimental rheumatoid arthritis
Rheumatoid arthritis (RA), characterized by chronic inflammation of synovial joints, is often associated with ongoing pain and increased pain sensitivity. High hydrogen ion concentration (acidosis) found in synovial fluid in RA patients is associated with disease severity. Acidosis signaling acting...
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Published in | Scientific reports Vol. 7; no. 1; pp. 8870 - 14 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Nature Publishing Group UK
21.08.2017
Nature Publishing Group Nature Portfolio |
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ISSN | 2045-2322 2045-2322 |
DOI | 10.1038/s41598-017-09200-6 |
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Abstract | Rheumatoid arthritis (RA), characterized by chronic inflammation of synovial joints, is often associated with ongoing pain and increased pain sensitivity. High hydrogen ion concentration (acidosis) found in synovial fluid in RA patients is associated with disease severity. Acidosis signaling acting on proton-sensing receptors may contribute to inflammation and pain. Previous studies focused on the early phase of arthritis (<5 weeks) and used different arthritis models, so elucidating the roles of different proton-sensing receptors in the chronic phase of arthritis is difficult. We intra-articularly injected complete Freund’s adjuvant into mice once a week for 4 weeks to establish chronic RA pain. Mice with knockout of acid-sensing ion channel 3 (ASIC3) or transient receptor potential/vanilloid receptor subtype 1 (TRPV1) showed attenuated chronic phase (>6 weeks) of RA pain. Mice with T-cell death-associated gene 8 (TDAG8) knockout showed attenuated acute and chronic phases of RA pain. TDAG8 likely participates in the initiation of RA pain, but all three genes, TDAG8, TRPV1, and ASIC3, are essential to establish hyperalgesic priming to regulate the chronic phase of RA pain. |
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AbstractList | Rheumatoid arthritis (RA), characterized by chronic inflammation of synovial joints, is often associated with ongoing pain and increased pain sensitivity. High hydrogen ion concentration (acidosis) found in synovial fluid in RA patients is associated with disease severity. Acidosis signaling acting on proton-sensing receptors may contribute to inflammation and pain. Previous studies focused on the early phase of arthritis (<5 weeks) and used different arthritis models, so elucidating the roles of different proton-sensing receptors in the chronic phase of arthritis is difficult. We intra-articularly injected complete Freund's adjuvant into mice once a week for 4 weeks to establish chronic RA pain. Mice with knockout of acid-sensing ion channel 3 (ASIC3) or transient receptor potential/vanilloid receptor subtype 1 (TRPV1) showed attenuated chronic phase (>6 weeks) of RA pain. Mice with T-cell death-associated gene 8 (TDAG8) knockout showed attenuated acute and chronic phases of RA pain. TDAG8 likely participates in the initiation of RA pain, but all three genes, TDAG8, TRPV1, and ASIC3, are essential to establish hyperalgesic priming to regulate the chronic phase of RA pain.Rheumatoid arthritis (RA), characterized by chronic inflammation of synovial joints, is often associated with ongoing pain and increased pain sensitivity. High hydrogen ion concentration (acidosis) found in synovial fluid in RA patients is associated with disease severity. Acidosis signaling acting on proton-sensing receptors may contribute to inflammation and pain. Previous studies focused on the early phase of arthritis (<5 weeks) and used different arthritis models, so elucidating the roles of different proton-sensing receptors in the chronic phase of arthritis is difficult. We intra-articularly injected complete Freund's adjuvant into mice once a week for 4 weeks to establish chronic RA pain. Mice with knockout of acid-sensing ion channel 3 (ASIC3) or transient receptor potential/vanilloid receptor subtype 1 (TRPV1) showed attenuated chronic phase (>6 weeks) of RA pain. Mice with T-cell death-associated gene 8 (TDAG8) knockout showed attenuated acute and chronic phases of RA pain. TDAG8 likely participates in the initiation of RA pain, but all three genes, TDAG8, TRPV1, and ASIC3, are essential to establish hyperalgesic priming to regulate the chronic phase of RA pain. Rheumatoid arthritis (RA), characterized by chronic inflammation of synovial joints, is often associated with ongoing pain and increased pain sensitivity. High hydrogen ion concentration (acidosis) found in synovial fluid in RA patients is associated with disease severity. Acidosis signaling acting on proton-sensing receptors may contribute to inflammation and pain. Previous studies focused on the early phase of arthritis (<5 weeks) and used different arthritis models, so elucidating the roles of different proton-sensing receptors in the chronic phase of arthritis is difficult. We intra-articularly injected complete Freund’s adjuvant into mice once a week for 4 weeks to establish chronic RA pain. Mice with knockout of acid-sensing ion channel 3 (ASIC3) or transient receptor potential/vanilloid receptor subtype 1 (TRPV1) showed attenuated chronic phase (>6 weeks) of RA pain. Mice with T-cell death-associated gene 8 (TDAG8) knockout showed attenuated acute and chronic phases of RA pain. TDAG8 likely participates in the initiation of RA pain, but all three genes, TDAG8, TRPV1, and ASIC3, are essential to establish hyperalgesic priming to regulate the chronic phase of RA pain. Abstract Rheumatoid arthritis (RA), characterized by chronic inflammation of synovial joints, is often associated with ongoing pain and increased pain sensitivity. High hydrogen ion concentration (acidosis) found in synovial fluid in RA patients is associated with disease severity. Acidosis signaling acting on proton-sensing receptors may contribute to inflammation and pain. Previous studies focused on the early phase of arthritis (<5 weeks) and used different arthritis models, so elucidating the roles of different proton-sensing receptors in the chronic phase of arthritis is difficult. We intra-articularly injected complete Freund’s adjuvant into mice once a week for 4 weeks to establish chronic RA pain. Mice with knockout of acid-sensing ion channel 3 (ASIC3) or transient receptor potential/vanilloid receptor subtype 1 (TRPV1) showed attenuated chronic phase (>6 weeks) of RA pain. Mice with T-cell death-associated gene 8 (TDAG8) knockout showed attenuated acute and chronic phases of RA pain. TDAG8 likely participates in the initiation of RA pain, but all three genes, TDAG8, TRPV1, and ASIC3, are essential to establish hyperalgesic priming to regulate the chronic phase of RA pain. |
ArticleNumber | 8870 |
Author | Sun, Wei-Hsin Kung, Chia-Chi Hsieh, Wei-Shan Lin, Shih-Chang Huang, Shir-Ly |
Author_xml | – sequence: 1 givenname: Wei-Shan surname: Hsieh fullname: Hsieh, Wei-Shan organization: Department of Life Sciences, National Central University – sequence: 2 givenname: Chia-Chi surname: Kung fullname: Kung, Chia-Chi organization: Department of Life Sciences, National Central University, Department of Anesthesiology, National Taiwan University Hospital Hsin-Chu Branch – sequence: 3 givenname: Shir-Ly surname: Huang fullname: Huang, Shir-Ly organization: Institute of Microbiology and Immunology, National Yang-Ming University – sequence: 4 givenname: Shih-Chang surname: Lin fullname: Lin, Shih-Chang organization: Department of Immunology, Cathy General Hospital – sequence: 5 givenname: Wei-Hsin orcidid: 0000-0003-3009-520X surname: Sun fullname: Sun, Wei-Hsin email: weihsin@cc.ncu.edu.tw organization: Department of Life Sciences, National Central University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28827659$$D View this record in MEDLINE/PubMed |
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Snippet | Rheumatoid arthritis (RA), characterized by chronic inflammation of synovial joints, is often associated with ongoing pain and increased pain sensitivity. High... Abstract Rheumatoid arthritis (RA), characterized by chronic inflammation of synovial joints, is often associated with ongoing pain and increased pain... |
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SubjectTerms | 13/51 42/89 631/378/1959/2605 64/60 692/699/1670/498 Acid Sensing Ion Channels - genetics Acid Sensing Ion Channels - metabolism Acidosis Animal models Animals Antigens, CD - metabolism Antigens, Differentiation, Myelomonocytic - metabolism Arthralgia - etiology Arthralgia - physiopathology Arthritis, Experimental Arthritis, Rheumatoid - complications Arthritis, Rheumatoid - genetics Arthritis, Rheumatoid - pathology Autoimmune diseases Biomarkers Capsaicin receptors Cell death Chronic pain Cytokines - blood Cytokines - metabolism Disease Models, Animal Female Gene Expression Humanities and Social Sciences Hydrogen ion concentration Hydrogen ions Hyperalgesia - etiology Hyperalgesia - physiopathology Immunohistochemistry Joint diseases Lymphocytes T Macrophages - immunology Macrophages - metabolism Macrophages - pathology Male Mice Mice, Knockout multidisciplinary Pain Receptors, G-Protein-Coupled - genetics Receptors, G-Protein-Coupled - metabolism Rheumatoid arthritis Science Science (multidisciplinary) Synovial fluid Transient receptor potential proteins TRPV Cation Channels - genetics TRPV Cation Channels - metabolism |
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Title | TDAG8, TRPV1, and ASIC3 involved in establishing hyperalgesic priming in experimental rheumatoid arthritis |
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