4.5 Article

Anti-Citrullinated Protein Antibodies Induce Macrophage Subset Disequilibrium in RA Patients

Journal

INFLAMMATION
Volume 38, Issue 6, Pages 2067-2075

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10753-015-0188-z

Keywords

rheumatoid arthritis; ACPAs; macrophage subset; IRF5

Funding

  1. National Natural Science Foundation Projects [C080102]
  2. Department of Education [Z2010008]
  3. Key Laboratory of Myocardial Ischemia, Harbin Medical University, Chinese Ministry of Education [KF201006, KF201203, KF201415]
  4. Heilongjiang province government [LRB 2010-393]

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We used samples from rheumatoid arthritis (RA) patients to examine whether Anti-citrullinated protein antibodies (ACPAs) alter macrophage subset distribution and promote RA development. Macrophage subset distributions and interferon regulatory factor 4 (IRF4) and IRF5 expressions were analyzed. ACPAs were purified by affinity column. After RA and osteoarthritis (OA) patients' macrophages were cocultured with ACPAs, macrophage subsets and IRF4 and IRF5 expressions were measured. Small interfering RNAs (siRNAs) were transfected into ACPA-activated cells to suppress IRF4 or IRF5. Fluorescence-activated cell sorting (FACS), Western blot, and immunohistochemistry were performed. Macrophage subset disequilibrium occurred in RA patient synovial fluids. IRF4 and IRF5 were all expressed in the synovial fluid and synovium. ACPAs (40 IU/ml) could induce macrophages to polarize to M1 subsets, and the percentage of increased M1/M2 ratio of RA patients was higher than that of the OA patients. ACPAs also induce IRF4 and IRF5 protein expressions. IRF5 siRNA transfection impaired ACPA activity significantly. We demonstrated that macrophage subset disequilibrium occurred in RA patients. ACPAs induced IRF5 activity and led to M1 macrophage polarization.

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