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 inScientific reports Vol. 7; no. 1; pp. 8870 - 14
Main Authors Hsieh, Wei-Shan, Kung, Chia-Chi, Huang, Shir-Ly, Lin, Shih-Chang, Sun, Wei-Hsin
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 21.08.2017
Nature Publishing Group
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ISSN2045-2322
2045-2322
DOI10.1038/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.
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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SSID ssj0000529419
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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...
SourceID doaj
pubmedcentral
proquest
pubmed
crossref
springer
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 8870
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
URI https://link.springer.com/article/10.1038/s41598-017-09200-6
https://www.ncbi.nlm.nih.gov/pubmed/28827659
https://www.proquest.com/docview/1957285037
https://www.proquest.com/docview/1931246147
https://pubmed.ncbi.nlm.nih.gov/PMC5566336
https://doaj.org/article/04687ec1ce824e0b918d143381fe6bb2
Volume 7
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