Publication: A role of oestrogen in aggravating SLE-like syndrome in C4-deficient mice
1
Issued Date
2015-12-01
Resource Type
ISSN
22288694
0125877X
0125877X
Other identifier(s)
2-s2.0-84955245372
Rights
Mahidol University
Rights Holder(s)
SCOPUS
Bibliographic Citation
Asian Pacific Journal of Allergy and Immunology. Vol.33, No.4 (2015), 339-348
Suggested Citation
Prapassorn Boonsoongnern, Tassanee Faisaikarm, Parisatcha Sangsuwan, Wattana Weerachatyanukul, Yindee Kitiyanant A role of oestrogen in aggravating SLE-like syndrome in C4-deficient mice. Asian Pacific Journal of Allergy and Immunology. Vol.33, No.4 (2015), 339-348. doi:10.12932/AP0624.33.4.2015 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/36033
Research Projects
Organizational Units
Authors
Journal Issue
Thesis
Title
A role of oestrogen in aggravating SLE-like syndrome in C4-deficient mice
Other Contributor(s)
Abstract
© 2009 is a Digital Portal of health science journals in Thailand. Background: As one of the epigenetic factors, oestrogen is considered to be a predisposing factor that is associated with a susceptibility to autoimmune disease development in women including systemic lupus erythematosus (SLE). Here, we proposed that oestrogen is also imparted in a post-lupus symptomatic enhancement as studied in the C4-deficient (C4-/-) mice model known to develop SLE-like symptoms. Methods: Fifty-six C4 knockout mice were ovariectomised (OVX) to eliminate the effect of endogenous feminine hormones followed by 17-β oestradiol (E2) administration in both dose- and time-dependent manners. Histopathological features of kidneys and spleens were studied by histological and immunofluorescent staining. The relative expression levels of IgG and IgM were measured densitometrically on their immunoreactive bands and the level of IgG-anti-double stranded (ds) DNA was measured by ELISA. Results: E2-treated mice displayed a gradual increase in immune complex deposition (both IgG and IgM) in glomeruli and proximal convoluted tubules. An increased reactivity of autoantibodies against dsDNA correlated with increasing doses and longer exposure to E2 treatments. In addition, enlargement of the spleen (splenomegaly) was also observed in E2- treated mice. Conclusions: Our results support the hypothesis that oestrogen aggravates severity of the SLElike symptoms in C4-deficient mice.
