Lupus progression deteriorates oogenesis quality in MRL/lpr mice.

Autor: Delimitreva S; Department of Biology, Medical University of Sofia, 2, Zdrave Str., 1431, Sofia, Bulgaria. s.delimitreva@medfac.mu-sofia.bg., Boneva G; Department of Immunology, Stefan Angelov Institute of Microbiology, Bulgarian Academy of Sciences, Acad. G. Bonchev Street, Block 26, 1113, Sofia, Bulgaria., Chakarova I; Department of Biology, Medical University of Sofia, 2, Zdrave Str., 1431, Sofia, Bulgaria., Hadzhinesheva V; Department of Biology, Medical University of Sofia, 2, Zdrave Str., 1431, Sofia, Bulgaria., Zhivkova R; Department of Biology, Medical University of Sofia, 2, Zdrave Str., 1431, Sofia, Bulgaria., Markova M; Department of Biology, Medical University of Sofia, 2, Zdrave Str., 1431, Sofia, Bulgaria., Nikolova V; Department of Biology, Medical University of Sofia, 2, Zdrave Str., 1431, Sofia, Bulgaria., Kolarov A; Department of Biology, Medical University of Sofia, 2, Zdrave Str., 1431, Sofia, Bulgaria., Mladenov N; Department of Biology, Medical University of Sofia, 2, Zdrave Str., 1431, Sofia, Bulgaria., Bradyanova S; Department of Immunology, Stefan Angelov Institute of Microbiology, Bulgarian Academy of Sciences, Acad. G. Bonchev Street, Block 26, 1113, Sofia, Bulgaria., Prechl J; R&D Laboratory, Diagnosticum Zrt, Budapest, Hungary., Mihaylova N; Department of Immunology, Stefan Angelov Institute of Microbiology, Bulgarian Academy of Sciences, Acad. G. Bonchev Street, Block 26, 1113, Sofia, Bulgaria., Tchorbanov A; Department of Immunology, Stefan Angelov Institute of Microbiology, Bulgarian Academy of Sciences, Acad. G. Bonchev Street, Block 26, 1113, Sofia, Bulgaria. tchorban@microbio.bas.bg.; National Institute of Immunology, 1517, Sofia, Bulgaria. tchorban@microbio.bas.bg.
Jazyk: angličtina
Zdroj: Immunologic research [Immunol Res] 2024 Aug; Vol. 72 (4), pp. 811-827. Date of Electronic Publication: 2024 May 21.
DOI: 10.1007/s12026-024-09489-2
Abstrakt: Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by the activation of the immune response against self antigens. Numerous reproductive complications, including reduced birth rate and complications for the mother and the fetus during pregnancy, have been observed in women with SLE. In the present study, we aimed to investigate the effect of SLE development on oocyte meiosis in lupus-prone mice. Lupus-prone MRL/lpr mice were used for the experiments: disease-free (4 weeks of age) and sick (20 weeks of age, virgin and postpartum). The immune response was monitored by flow cytometry, ELISpot, ELISA, and histology. Oocytes were analyzed by fluorescence microscopy based on chromatin, tubulin, and actin structures. The lupus-prone MRL/lpr mice developed age-dependent symptoms of SLE with increased levels of various autoantibodies, proteinuria, and renal infiltrates and a tendency for the immune response to worsen with changes in cell populations and the cytokine profile. The number and quality of oocytes were also affected, and the successful pregnancy rate of MRL/lpr mice was limited to only 60%. Isolated oocytes showed severe structural changes in all studied groups. Systemic alterations in immune homeostasis in SLE affect the quality of developing oocytes, which is evident from a young age. The data obtained is in line with the trend of reduced fertility in lupus-prone MRL/lpr mice. The phenomenon can be explained by changes in the microenvironment of the relevant organs and close connection between ovulation and inflammatory processes.
(© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
Databáze: MEDLINE
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