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Sex-Related Differences in the Morphology and Subpopulation Composition of Colon Lymphocytes in Experimental Acute Colitis

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Morphological manifestations of acute colitis and subpopulation composition of colon lymphocytes were studied in male and female C57Bl/6 mice with acute dextran-induced colitis. We evaluated the severity of colitis symptoms, morphological changes in the colon, and prevalence of epithelialized and non-epithelialized ulcers. The subpopulation composition of lymphocytes (CD3—CD19+ B cells, CD3+CD4+ T helpers, CD3+CD8+ cytotoxic T cells, and CD4+CD25+FOXP3+ regulatory T cells) was assessed by flow cytofluorometry in suspension of colon cells prepared by enzymatic disintegration. In males, clinical manifestations of acute colitis and morphological changes were more severe and the prevalence of non-epithelialized ulcers was higher than in females. In females, the content of T, B, and regulatory T cells in the colon wall was higher, while the content of cytotoxic T cells was lower than in males. In females with acute colitis, the absolute lymphocyte count and the content of B cells and regulatory T cells decreased, while the percentage of cytotoxic T cells increased in comparison with intact animals. In males with acute colitis, the levels of regulatory T and B cells increased in comparison with the corresponding parameter in intact animals. Morphological changes and changes in the lymphocyte subpopulations, detected in males and females with acute colitis, were determined by different levels of sex steroid hormones.

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References

  1. Gao Y, Postovalova EA, Dobrynina MT, Makarova OV. Sexrelated differences in morphological changes and immune disorders during experimental acute ulcerative colitis. Klin. Eksp. Morfol. 2016;17(1):37-43. Russian.

    Google Scholar 

  2. Kosyreva AM1, Simonova EY, Makarova OV. Sex differences in pulmonary and immune response in acute experimental endotoxicosis. Bull. Exp. Biol. Med. 2012;153(3):340-342.

    Article  PubMed  CAS  Google Scholar 

  3. Makarova OV, Postovalova EA. Morphological Changes in the Thymus, Composition of Its Cells, and Subpopulations of Peripheral Blood Lymphocytes during Experimental Acute Ulcerative Colitis. Bull. Exp. Biol. Med. 2017;163(5):681-686.

    Article  PubMed  CAS  Google Scholar 

  4. Angele MK, Frantz MC, Chaudy IH. Sex and sex hormones influence the response to trauma and sepsis: potential therapeutic approaches. Clinics (San Paulo). 2006;61(5):479-488.

    Google Scholar 

  5. Bábíčková J, Tóthová Ľ, Lengyelová E, Bartoňová A, Hodosy J, Gardlík R, Celec P. Sex Differences in experimentally induced colitis in mice: a role for estrogens. Inflammation. 2015;38(5):1996-2006.

    Article  PubMed  CAS  Google Scholar 

  6. Fish EN. The X-files in immunity: sex-based differences predispose immune responses. Nat. Rev. Immunol. 2008;8(9):737-744.

    Article  PubMed  CAS  Google Scholar 

  7. Foo YZ, Nakagawa S, Rhodes G, Simmons LW. The effects of sex hormones on immune function: a meta-analysis. Biol. Rev. Camb. Philos. Soc. 2017;92(1):551-571.

    Article  PubMed  Google Scholar 

  8. Kissicka HT, Sandab MG, Dunn LK, Pellegrini KL, On ST, Noel JK, Arredouani MS. Androgens alter T-cell immunity by inhibiting T-helper 1 differentiation. Proc. Natl Acad. Sci. USA. 2014;111(27):9887-9892.

    Article  CAS  Google Scholar 

  9. Okayasu I, Hatakeyama S, Yamada M, Ohkusa T, Inagaki Y, Nakaya R. A novel method in the induction of reliable experimental acute and chronic ulcerative colitis in mice. Gastroenterology. 1990;98(3):694-702.

    Article  PubMed  CAS  Google Scholar 

  10. Roved J, Westerdahl H, Hasselquist D. Sex differences in immune responses: Hormonal effects, antagonistic selection, and evolutionary consequences. Horm. Behav. 2017;88:95-105.

    Article  PubMed  CAS  Google Scholar 

  11. Walecki M, Eisel F, Klug J, Baal N, Paradowska-Dogan A, Wahle E, Hackstein H, Meinhardt A, Fijak M. Androgen receptor modulates Foxp3 expression in CD4+CD25+Foxp3+ regulatory T-cells. Mol. Biol. Cell. 2015;26(15):2845-2857.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  12. Weigmann B, Tubbe I, Seidel D, Nicolaev A, Becker C, Neurath MF. Isolation and subsequent analysis of murine lamina propria mononuclear cells from colon tissue. Nat. Protoc. 2007;2(10):2307-2311.

    Article  PubMed  CAS  Google Scholar 

  13. Zuk M, Stoehr AM. Sex Differences in susceptibility to infection: an evolutionary perspective. Sex Hormones and immunity to Infection. Klein SL, Roberts CW, eds. Heidelberg, 2010. P. 1-17.

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Correspondence to E. A. Postovalova.

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Translated from Byulleten’ Eksperimental’noi Biologii i Meditsiny, Vol. 165, No. 4, pp. 500-504, April, 2018

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Gao, Y., Postovalova, E.A., Makarova, O.V. et al. Sex-Related Differences in the Morphology and Subpopulation Composition of Colon Lymphocytes in Experimental Acute Colitis. Bull Exp Biol Med 165, 503–507 (2018). https://doi.org/10.1007/s10517-018-4204-9

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  • DOI: https://doi.org/10.1007/s10517-018-4204-9

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