2026-09-21T19:47:56Zhttps://gupea.ub.gu.se/server/oai/request

oai:gupea.ub.gu.se:2077/351972014-04-26T01:30:29Zcom_2077_283com_2077_17com_2077_10556col_2077_543col_2077_310col_2077_10557

Stubelius, Alexandra 2014-04-25T06:36:47Z 2014-04-25T06:36:47Z 2014-04-25 978-91-628-8945-6 http://hdl.handle.net/2077/35197 Rheumatoid arthritis (RA) is characterized by severe synovial inflammation, cartilage destruction, and immune-mediated bone loss. Estrogen ameliorates experimental RA, reducing both inflammation and bone loss. The inflamed tissues are damaged partly by innate immune cells producing reactive oxygen species (ROS). ROS can also regulate the immune system. This thesis aimed to investigate the regulation of inflammation and joint destruction by 17β-estradiol (E2) and its metabolite 2-methoxyestradiol (2me2). E2's and 2me2's immunomodulation were investigated both in experimental arthritis and in an unprovoked immune system. Both wild type (WT) mice and Catechol-O-methyltransferase (COMT)-deficient mice were used, as COMT metabolizes E2 into 2me2. Further, E2's regulatory role was investigated in WT mice or ROS-deficient mice (B10.Q.Ncf1*/*), in a model of osteoporosis and a local (LPS-induced) inflammation model. 2me2 ameliorated arthritis and bone mineral density (BMD), and regulated immune cells differently compared with E2. Treatment with high doses of 2me2 increased uteri weight, implying estrogen-receptor activation; 2me2 activated estrogen-response elements in a tissue-, and dose-dependent manner. Deficiency in the COMT enzyme only moderately affected the immune system, and males were more affected than females. In ovx-induced bone loss, ROS-deficient mice displayed reduced osteoclastogenesis compared to controls, but similar bone mineral density and immunological profiles. In LPS-induced inflammation, E2 treatment in WT mice shifted neutrophil infiltration to macrophage infiltration, while in ROS-deficient mice E2 treatment induced neutrophil infiltration and reduced the macrophages. In conclusion, E2's metabolite 2me2 can modulate arthritis and inflammation-triggered osteoporosis. At high doses 2me2 can induce estrogen receptor signaling. E2 together with ROS regulate inflammation and osteoclastogenesis. Understanding estrogenic cellular and molecular mechanisms are important for developing new arthritis and inflammationtreatments. Our results increase the understanding of estrogens' role in inflammation and motivate further investigations. eng I. Alexandra Stubelius, Emil Andréasson, Anna Karlsson, Claes Ohlsson, Åsa Tivesten, Ulrika Islander, Hans Carlsten. Role of 2-methoxyestradiol as inhibitor of arthritis and osteoporosis in a model of postmenopausal rheumatoid arthritis. Clinical Immunology 2011: 140, 37-46. ::doi:: 10.1016/j.clim.2011.03.006 II. Alexandra Stubelius, Malin C. Erlandsson, Ulrika Islander, Hans Carlsten. Immunomodulation by the estrogen metabolite 2-methoxyestradiol. Clinical Immunology 2014, in press. ::doi:: 10.1016/j.imbio.2012.04.010 III. Alexandra Stubelius, Anna S. Wilhelmson, Joseph A. Gogos, Åsa Tivesten, Ulrika Islander, Hans Carlsten. Sexual dimorphisms in the immune system of catechol-O-methyltransferase knockout mice. Immunobiology 2012: 217, 751-760. ::doi:: 10.1016/j.clim.2014.03.011 IV. Alexandra Stubelius, Annica Andersson, Rikard Holmdahl, Claes Ohlsson, Ulrika Islander, Hans Carlsten NADPH oxidase 2 influences osteoclast formation but is not critical for ovariectomy-induced bone loss. Manuscript V. Alexandra Stubelius, Annica Andersson, Rikard Holmdahl, Ulrika Islander, Hans Carlsten. Role of estrogen in regulating LPS-induced inflammation in NADPH oxidase 2 deficient mice. Manuscript Rheumatoid arthritis Estrogens 2-methoxyestradiol Innate immune system Inflammation Reactive oxygen species Osteoimmunology Osteoclasts Estrogen and 2-methoxyestradiol: regulation of arthritis, inflammation and reactive oxygen species text Doctoral thesis Doctor of Philosophy (Medicine) alexandra.stubelius@rheuma.gu.se University of Gothenburg. Sahlgrenska Academy Institute of Medicine. Department of Rheumatology and Inflammation Research Fredagen den 16 maj 2014, kl. 9.00, Föreläsningssalen vån 3 Guldhedsgatan 10A 2014-05-16 SA open.access