Expression of arginase 1 and tyrosine kinase Mer by blood monocytes in the dynamics of physiological pregnancy

E. Shevela, N. G. Bukhtueva, M. Tikhonova, L. Sakhno, N. Pasman, E. Chernykh
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Abstract

During pregnancy, the maternal immune system must maintain tolerance to paternal antigens, at the same time being able to eliminate pathogens, which is achieved by the weakening of adoptive immunity and the activation of innate immunity, in particular, monocytes. However, the question about the functional phenotype of monocytes, having not only pro-inflammatory, but also anti-inflammatory activity, remains open. In the given work, we have investigated the expression of M2-associated suppressive markers Arg1 and MerTK in monocyte subpopulations during uncomplicated pregnancy. Fifty-three pregnant women with uncomplicated gestation were recruited, including 14 pregnant in the 1st trimester, 20 – in the 2nd and 19 – in the third pregnancy trimester. The comparison group consisted of 15 fertile unpregnant women without aggravated somatic anamnesis, with a history of at least one childbirth. The findings showed that in the unpregnant group circulating Mo express Arg1 and MerTK, and the most relative number of Arg1+ and MerTK+ cells is concentrated in intermediate and nonclassic monocytes. During pregnancy the expression of researched molecules in monocytes reliably increases. An increase in MerTK expression is manifested by a simultaneous increase in the number of MerTK+ cells and the mean fluorescence intensity of this marker; it is observed in the 1st and 2nd trimesters and registered in all three monocyte subpopulations. At the same time, an increase in Arg1 expression is manifested either by an enhancement of Arg1+ cells, or an increase in receptor density; it is registered throughout pregnancy, including the 3rd trimester, and is maximally expressed in classic monocytes. There is a direct correlation between the number of Arg1+ and MerTK+ cells in intermediate Mo, which increases with the progression of pregnancy, and in the 3rd trimester is also detected in classical and non-classical Mo. In general, the revealed increase in the expression of Arg1 and MerTK by monocytes indicates an increase in the anti-inflammatory potential of monocytes during pregnancy, and the involvement of monocytes in the regulation of the inflammatory process at the system level. Moreover, the features of Arg1 and MerTK expression in various monocyte subpopulations during pregnancy suggest that monocytes expressing Arg1 and MerTK can mediate different mechanisms of immune adaptation during pregnancy.
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精氨酸酶1和酪氨酸激酶Mer在生理性妊娠过程中单核细胞的表达
在怀孕期间,母体免疫系统必须保持对父本抗原的耐受性,同时能够消除病原体,这是通过削弱过继免疫和激活先天免疫,特别是单核细胞来实现的。然而,关于单核细胞功能表型的问题,不仅具有促炎活性,而且具有抗炎活性,仍然是开放的。在本研究中,我们研究了m2相关抑制标记Arg1和MerTK在单核细胞亚群中的表达。研究招募了53名妊娠无并发症的孕妇,包括14名妊娠早期的孕妇,20名妊娠晚期的孕妇和19名妊娠晚期的孕妇。对照组包括15名没有加重躯体性记忆的有生育能力的未怀孕妇女,至少有一次分娩史。结果显示,在未妊娠组循环Mo中,Arg1和MerTK均有表达,且Arg1+和MerTK+细胞的相对数量主要集中在中间和非经典单核细胞中。在怀孕期间,研究分子在单核细胞中的表达确实增加。MerTK表达增加表现为MerTK+细胞数量和该标记物的平均荧光强度同时增加;它在妊娠的第一和第二阶段被观察到,并且在所有三个单核细胞亚群中都有记录。同时,Arg1表达的增加表现为Arg1+细胞的增强或受体密度的增加;它在整个妊娠期间都有记录,包括妊娠晚期,并在经典单核细胞中最大程度地表达。中间胎Mo中Arg1+和MerTK+细胞的数量直接相关,随着妊娠的进展而增加,在妊娠晚期经典胎Mo和非经典胎Mo中也检测到Arg1和MerTK的表达增加。总的来说,单核细胞表达Arg1和MerTK的增加表明妊娠期间单核细胞的抗炎潜能增加,单核细胞在系统水平上参与了炎症过程的调节。此外,Arg1和MerTK在妊娠期不同单核细胞亚群中的表达特点表明,表达Arg1和MerTK的单核细胞可以介导妊娠期不同的免疫适应机制。
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来源期刊
Medical Immunology (Russia)
Medical Immunology (Russia) Medicine-Immunology and Allergy
CiteScore
0.70
自引率
0.00%
发文量
88
审稿时长
12 weeks
期刊介绍: The journal mission is to promote scientific achievements in fundamental and applied immunology to various medical fields, the publication of reviews, lectures, essays by leading domestic and foreign experts in the field of fundamental and experimental immunology, clinical immunology, allergology, immunodiagnostics and immunotherapy of infectious, allergy, autoimmune diseases and cancer.
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