INFLUENCE OF ENDOCRINE PATHOLOGY ON NEUROIMMOUNS INTERACTIONS IN PLACENTA

Cover Page

Cite item

Full Text

Abstract

According to statistics, approximately 75-80% of cases of diabetes mellitus in women during pregnancy show the presence of a urogenital infection in which the development of the inflammatory process is conducive to the elimination of the pathogen and the appearance of necrotic tissue. Such inflammatory processes, as a rule, occur with the participation of macrophages attracted by B-lymphocytes and NK-cells. The main goal of this study was to evaluate the expression ratio of immunocompetent cells: macrophages, NK cells and B lymphocytes in the placenta in women with diabetes mellitus who are in different age groups. Molecular markers were visualized using an immunoistochemical method. Were used antibodies to CD68 (1:300, Dako, USA) for macrophages, CD20 (1:300, Dako, USA) for B-lymphocytes and CD57 (1:300, Dako, USA) for natural killer cells. The results were visualized on a confocal microscope (FluoView 1000 (Olympus)). For scoring of microphotographs program “Morphology 5.2” was used. On the microphotographs the relative area of expression was evaluated, signified as the ratio of the area of the immunopositive reaction to the total area of the slide and the optical density. Then a statistical evaluation of the obtained data in the “Statistic 10.0” program was carried out. During the experiment, a sharp decrease in the expression of the CD68 marker in the placenta was detected. A decrease in the expression of the CD20 marker with an increase in the age of patients with diabetes mellitus was also demonstrated, while in healthy women an increase was observed in the middle age group. For natural killers, there was no difference between healthy and sick women. The result indicates a weakening of the reaction of the immune system in diabetes mellitus.

Full Text

Introduction. According to literature, during pregnancy in women with concomitant disease such as diabetes mellitus in 75-80% of cases urogenital infection is verified, which is accompanied by inflammation and the occurrence of necrotic areas [1-3]. As a rule, inflammatory processes caused by the participation of macrophages attracted by B lymphocytes and NK cells. Placental macrophages - the main immunocompetent cells in the placenta that carry out reactions of innate immunity. According to numerous literature data, the number of macrophages during the whole pregnancy does not change [1, 3]. Another component of the maternal immune response to infection is natural killer cells (NK cells), it is known that these cells in the mature placenta are extremely rarely verified. B-lymphocytes belong to adaptive immunity and are almost completely absent in the placenta [2]. The aim of this work is to study the equilibration of immunocompetent cells: macrophages, NK cells and B lymphocytes in the placenta of women with diabetes mellitus different age groups. Material and metods. The material for the study was the placenta taken from women belonging to two nosological groups. The first group consisted of women with an established f diabetes, the second - the control group (healthy). Each group included 30 people. Both groups were further divided into 3 age periods - 18-28, 29-35 and 36-40 years, respectively. Molecular markers were visualized using an immunoistochemical method. Were used antibodies to CD68 (1:300, Dako, USA) for macrophages, CD20 (1:300, Dako, USA) for B-lymphocytes and CD57 (1:300, Dako, USA) for natural killer cells. The results were visualized on a confocal microscope (FluoView 1000 (Olympus)). For scoring of microphotographs program “Morphology 5.2” was used. On the microphotographs the relative area of expression was evaluated, signified as the ratio of the area of the immunopositive reaction to the total area of the slide and the optical density. Then a statistical evaluation of the obtained data in the “Statistic 10.0” program was carried out. Results and discussion. During the experiment, the presence of macrophages in control group was revealed, exclusively in the first age group. Their relative area expression was approximately 0.90 ± 0.3%. In the second and third age groups, macrophages were not verified. In the placenta of diabetic women, a significant decrease in the level of macrophages with increasing age of the patients was recorded. This indicator was 2.90 ± 0.89%, 2.20 ± 0.67%, 1.81 ± 0.43% for groups 18-28, 29-35 and 36-40 years, respectively. In terms of optical density in the control group, there were no significant differences in the expression of the CD20 marker between women of different age groups 18-28 and 29-35 years, however a significant decrease in this indicator was detected in the group of women of the older age - 36-40 years. For all 3 age groups, the optical density was 0.26 ± 0.09%, 0.25 ± 0.05%, 0.12 ± 0.1%, respectively. In the experimental group, twice increase in the expression index of CD20 in women aged 29-35 years, which was 0.9 ± 0.07%, was found; there were no differences between the groups of 18-28 and 36-40 years. The expression of the CD57 marker in both groups was positively correlated with an increase in the age of the patients. For the control group, the optical density index was 0.1 ± 0.03%, 0.18 ± 0.06% and 0.43 ± 0.09%. The index of optical density in placenta of women with diabetes tendency to decrease was revealed compared to the first group and was equal to 0.16 ± 0.01%, 0.2 ± 0.05% and 0.47 ± 0.1%, respectively. Conclusion. The results obtained in investigation suggest that diabetes mellitus, during pregnancy, reduces immune responses not only locally, but also in the body as a whole. This trend is manifest as a sharp decrease in the expression of the CD68 marker in the placenta. The study showed a significant decrease in the expression of the CD20 marker, correlating with an increase in the age of patients with diabetes mellitus, whereas in women with uncomplicated pregnancy an increase in the B-lymphocyte marker was observed in the middle age group. For natural killers, no significant differences in the studied groups were verified.
×

About the authors

A O Drobintseva

Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott, Saint Petersburg; Saint Petersburg Medical and Social Institute, Saint Petersburg

A E Andreev

Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott, Saint Petersburg; Saint Petersburg Medical and Social Institute, Saint Petersburg

S V Makarenko

Saint Petersburg Medical and Social Institute, Saint Petersburg

D S Medvedev

Saint Petersburg Medical and Social Institute, Saint Petersburg

Y A Soldatova

Saint Petersburg Medical and Social Institute, Saint Petersburg

V O Polyakova

Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott, Saint Petersburg; Saint Petersburg Medical and Social Institute, Saint Petersburg; Saint Petersburg State University, Saint Petersburg

References

  1. Edu A, Teodorescu C, Dobjanschi CG, et al. Placenta changes in pregnancy with gestational diabetes. Rom J Morphol Embryol. 2016;57(2):507-12.
  2. Radaelli T, Varastehpour A, Catalano P, Hauguel-de Mouzon S. Gestational diabetes induces placental genes for chronic stress and inflammatory pathways. Diabetes. 2003;52(12):2951-2958.
  3. Jun Y, Yong Z, Juan G, et al. Assessment of the number and function of macrophages in the placenta of gestational diabetes mellitus patients. Journal of Huazhong University of Science and Technology. 2013;33(5):725-729.

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2019 Drobintseva A.O., Andreev A.E., Makarenko S.V., Medvedev D.S., Soldatova Y.A., Polyakova V.O.

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

СМИ зарегистрировано Федеральной службой по надзору в сфере связи, информационных технологий и массовых коммуникаций (Роскомнадзор).
Регистрационный номер и дата принятия решения о регистрации СМИ: серия ПИ № ФС 77 - 74760 от 29.12.2018 г.


This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies