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  1. 1
    Academic Journal

    Source: Obstetrics, Gynecology and Reproduction; Online First ; Акушерство, Гинекология и Репродукция; Online First ; 2500-3194 ; 2313-7347

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    Relation: https://www.gynecology.su/jour/article/view/2566/1382; Сотникова Н.Ю., Малышкина А.И., Куст А.В., Воронин Д.Н. Анализ дифференцировки периферических B-лимфоцитов у женщин с угрожающим самопроизвольным выкидышем и привычным невынашиванием беременности в анамнезе. Сибирский научный медицинский журнал. 2021;41(3):38–44. https://doi.org/10.18699/SSMJ20210305.; Галкина Д.Е., Макаренко Т.А., Окладников Д.В. Иммунологические аспекты нормальной и патологически протекающей беременности. Вестник Российской академии медицинских наук. 2022;77(1):13–24. https://doi.org/10.15690/vramn1507.; Ticconi C., Di Simone N., Campagnolo L., Fazleabas A. Clinical consequences of defective decidualization. Tissue Cell. 2021;72:101586. https://doi.org/10.1016/j.tice.2021.101586.; Saribas G.S., Akarca Dizakar O., Ozogul C. et al. Ellagic acid increases implantation rates with its antifibrotic effect in the rat model of intrauterine adhesion. Pathol Res Pract. 2023;246:154499. https://doi.org/10.1016/j.prp.2023.154499.; Марьин А.А., Танцерева И.Г., Большаков В.В., Коломиец Н.Э. Лекарственные растения в коррекции климактерических расстройств. Фундаментальная и клиническая медицина. 2019;4(1):80–90.; Arck P.C., Hecher K. Fetomaternal immune cross-talk and its consequences for maternal and offspring's health. Nat Med. 2013;19(5):548–56. https://doi.org/10.1038/nm.3160.; Vacca P., Vitale C., Montaldo E. et al. CD34+ hematopoietic precursors are present in human decidua and differentiate into natural killer cells upon interaction with stromal cells. Proc Natl Acad Sci U S A. 2011;108(6):2402–7. https://doi.org/10.1073/pnas.1016257108.; Acar N., Ustunel I., Demir R. Uterine natural killer (uNK) cells and their missions during pregnancy: a review. Acta Histochem. 2011;113(2):82–91. https://doi.org/10.1016/j.acthis.2009.12.001.; Kopcow H.D., Allan D.S., Chen X. et al. Human decidual NK cells form immature activating synapses and are not cytotoxic. Proc Natl Acad Sci U S A. 2005;102(43):15563–8. https://doi.org/10.1073/pnas.0507835102.; Huhn O., Zhao X., Esposito L. et al. How do uterine natural killer and innate lymphoid cells contribute to successful pregnancy? Front Immunol. 2021;12:607669. https://doi.org/10.3389/fimmu.2021.607669.; Zhang X., Wei H. Role of decidual natural killer cells in human pregnancy and related pregnancy complications. Front Immunol. 2021;12:728291. https://doi.org/10.3389/fimmu.2021.728291.; Chao K.H., Yang Y.S., Ho H.N. et al. Decidual natural killer cytotoxicity decreased in normal pregnancy but not in anembryonic pregnancy and recurrent spontaneous abortion. Am J Reprod Immunol. 1995;34(5):274–80. https://doi.org/10.1111/j.1600-0897.1995.tb00953.x.; King A., Birkby C., Loke Y.W. Early human decidual cells exhibit NK activity against the K562 cell line but not against first trimester trophoblast. Cell Immunol. 1989;118(2):337–44. https://doi.org/10.1016/0008-8749(89)90382-1.; Sojka D.K., Yang L., Plougastel-Douglas B. et al. Cutting edge: local proliferation of uterine tissue-resident NK cells during decidualization in mice. J Immunol. 2018;201(9):2551-2556. https://doi.org/10.4049/jimmunol.1800651.; Sojka D.K., Yang L., Yokoyama W.M. Uterine natural killer cells. Front Immunol. 2019;10:960. https://doi.org/10.3389/fimmu.2019.00960.; Gamliel M., Goldman-Wohl D., Isaacson B. et al. Trained memory of human uterine NK cells enhances their function in subsequent pregnancies. Immunity. 2018;48(5):951–962.e5. https://doi.org/10.1016/j.immuni.2018.03.030.; Prefumo F., Ganapathy R., Thilaganathan B., Sebire N.J. Influence of parity on first trimester endovascular trophoblast invasion. Fertil Steril. 2006;85(4):1032–6. https://doi.org/10.1016/j.fertnstert.2005.09.055.; Ashkar A.A., Di Santo J.P., Croy B.A. Interferon gamma contributes to initiation of uterine vascular modification, decidual integrity, and uterine natural killer cell maturation during normal murine pregnancy. J Exp Med. 2000;192(2):259–70. https://doi.org/10.1084/jem.192.2.259.; Ruiz J.E., Kwak J.Y., Baum L. et al. Effect of intravenous immunoglobulin G on natural killer cell cytotoxicity in vitro in women with recurrent spontaneous abortion. J Reprod Immunol. 1996;31(1–2):125–41. https://doi.org/10.1016/0165-0378(96)00969-2.; Kuroda K., Venkatakrishnan R., James S. et al. Elevated periimplantation uterine natural killer cell density in human endometrium is associated with impaired corticosteroid signaling in decidualizing stromal cells. J Clin Endocrinol Metab. 2013;98(11):4429–37. https://doi.org/10.1210/jc.2013-1977.; Wilkens J., Male V., Ghazal P. et al. Uterine NK cells regulate endometrial bleeding in women and are suppressed by the progesterone receptor modulator asoprisnil. J Immunol. 2013;191(5):2226–35. https://doi.org/10.4049/jimmunol.1300958.; Kalkunte S.S., Mselle T.F., Norris W.E. еt al. Vascular endothelial growth factor C facilitates immune tolerance and endovascular activity of human uterine NK cells at the maternal-fetal interface. J Immunol. 2009;182(7):4085–92. https://doi.org/10.4049/jimmunol.0803769.; Zhou Y., Fisher S.J., Janatpour M. et al. Human cytotrophoblasts adopt a vascular phenotype as they differentiate. A strategy for successful endovascular invasion? J Clin Invest. 1997;99(9):2139–51. https://doi.org/10.1172/JCI119387.; Co E.C., Gormley M., Kapidzic M. et al. Maternal decidual macrophages inhibit NK cell killing of invasive cytotrophoblasts during human pregnancy. Biol Reprod. 2013;88(6):155. https://doi.org/10.1095/biolreprod.112.099465.; Liu Y., Gao S., Zhao Y. et al. Decidual natural killer cells: a good nanny at the maternal-fetal interface during early pregnancy. Front Immunol. 2021;12:663660. https://doi.org/10.3389/fimmu.2021.663660.; King A., Allan D.S., Bowen M. et al. HLA-E is expressed on trophoblast and interacts with CD94/NKG2 receptors on decidual NK cells. Eur J Immunol. 2000;30(6):1623–31. https://doi.org/10.1002/1521-4141(200006)30:63.0.CO;2-M.; Shojaei Z., Jafarpour R., Mehdizadeh S. et al. Functional prominence of natural killer cells and natural killer T cells in pregnancy and infertility: а comprehensive review and update. Pathol Res Pract. 2022;238:154062. https://doi.org/10.1016/j.prp.2022.154062.; Martin P., Gurevich D.B. Macrophage regulation of angiogenesis in health and disease. Semin Cell Dev Biol. 2021;119:101–10. https://doi.org/10.1016/j.semcdb.2021.06.010.; Li X.F., Charnock-Jones D.S., Zhang E. et al. Angiogenic growth factor messenger ribonucleic acids in uterine natural killer cells. J Clin Endocrinol Metab. 2001;86(4):1823–34. https://doi.org/10.1210/jcem.86.4.7418.; El-Azzamy H., Dambaeva S.V., Katukurundage D. et al. Dysregulated uterine natural killer cells and vascular remodeling in women with recurrent pregnancy losses. Am J Reprod Immunol. 2018;80(4):e13024. https://doi.org/10.1111/aji.13024.; Quenby S., Kalumbi C., Bates M. et al. Prednisolone reduces preconceptual endometrial natural killer cells in women with recurrent miscarriage. Fertil Steril. 2005;84(4):980–4. https://doi.org/10.1016/j.fertnstert.2005.05.012.; Tuckerman E., Mariee N., Prakash A. et al. Uterine natural killer cells in peri-implantation endometrium from women with repeated implantation failure after IVF. J Reprod Immunol. 2010;87(1–2):60–6. https://doi.org/10.1016/j.jri.2010.07.001.; Michimata T., Ogasawara M.S., Tsuda H. et al. Distributions of endometrial NK cells, B cells, T cells, and Th2/Tc2 cells fail to predict pregnancy outcome following recurrent abortion. Am J Reprod Immunol. 2002;47(4):196–202. https://doi.org/10.1034/j.1600-0897.2002.01048.x.; Lachapelle M.H., Miron P., Hemmings R., Roy D.C. Endometrial T, B, and NK cells in patients with recurrent spontaneous abortion. Altered profile and pregnancy outcome. J Immunol. 1996;156(10):4027–34.; Li H., Hou Y., Zhang S. et al. CD49a regulates the function of human decidual natural killer cells. Am J Reprod Immunol. 2019;81(4):e13101. https://doi.org/10.1111/aji.13101; Guo W., Fang L., Li B. et al. Decreased human leukocyte antigen-G expression by miR-133a contributes to impairment of proinvasion and proangiogenesis functions of decidual NK cells. Front Immunol. 2017;8:741. https://doi.org/10.3389/fimmu.2017.00741.; Маев И.В., Андреев Д.Н., Кучерявый Ю.А. Инфекция Helicobacter pylori и экстрагастродуоденальные заболевания. Терапевтический архив. 2015;87(8):103–10. https://doi.org/10.17116/terarkh2015878103-110.; Tossetta G., Fantone S., Giannubilo S.R. et al. Pre-eclampsia onset and SPARC: a possible involvement in placenta development. J Cell Physiol. 2019;234(5):6091–8. https://doi.org/10.1002/jcp.27344.; Croy B.A., van den Heuvel M.J., Borzychowski A.M., Tayade C. Uterine natural killer cells: a specialized differentiation regulated by ovarian hormones. Immunol Rev. 2006;214:161–85. https://doi.org/10.1111/j.1600-065X.2006.00447.x.; Kieckbusch J., Gaynor L.M., Moffett A., Colucci F. MHC-dependent inhibition of uterine NK cells impedes fetal growth and decidual vascular remodelling. Nat Commun. 2014;5:3359. https://doi.org/10.1038/ncomms4359.; Moffett A., Shreeve N. First do no harm: uterine natural killer (NK) cells in assisted reproduction. Hum Reprod. 2015;30(7):1519–25. https://doi.org/10.1093/humrep/dev098.; Fukui A., Funamizu A., Yokota M. et al. Uterine and circulating natural killer cells and their roles in women with recurrent pregnancy loss, implantation failure and preeclampsia. J Reprod Immunol. 2011;90(1):105–10. https://doi.org/10.1016/j.jri.2011.04.006.; Zhang J., Dunk C.E., Shynlova O. et al. TGFb1 suppresses the activation of distinct dNK subpopulations in preeclampsia. EBioMedicine. 2019;39:531–9. https://doi.org/10.1016/j.ebiom.2018.12.015.; Du M., Wang W., Huang L. et al. Natural killer cells in the pathogenesis of preeclampsia: a double-edged sword. J Matern Fetal Neonatal Med. 2022;35(6):1028–35. https://doi.org/10.1080/14767058.2020.1740675.; Saghafian Larijani S., Biglari E., Biglarifar R. The correlation between serum sodium levels and preeclampsia severity in pregnant women: a cross-sectional study. J Renal Inj Prev. 2025;14(4):e38440. https://doi.org/10.34172/jrip.2025.38440.; Габидуллина Р.И., Кошельникова Е.А., Шигабутдинова Т.Н. и др. Эндометриоз: влияние на фертильность и исходы беременности. Гинекология. 2021;23(1):12–7. https://doi.org/10.26442/20795696.2021.1.200477.; Pant A., Moar K., Arora T.K., Maurya P.K. Implication of biosignatures in the progression of endometriosis. Pathol Res Pract. 2024;254:155103. https://doi.org/10.1016/j.prp.2024.155103.; Giuliani E., Parkin K.L., Lessey B.A. et al. Characterization of uterine NK cells in women with infertility or recurrent pregnancy loss and associated endometriosis. Am J Reprod Immunol. 2014;72(3):262–9. https://doi.org/10.1111/aji.12259.; Thiruchelvam U., Wingfield M., O'Farrelly C. Increased uNK progenitor cells in Women with endometriosis and Infertility are associated with low levels of endometrial stem cell factor. Am J Reprod Immunol. 2016;75(4):493–502. https://doi.org/10.1111/aji.12486.; Pašalić E., Tambuwala M.M., Hromić-Jahjefendić A. Endometriosis: classification, pathophysiology, and treatment options. Pathol Res Pract. 2023;251:154847. https://doi.org/10.1016/j.prp.2023.154847.; Tang A.W., Alfirevic Z., Turner M.A. et al. A feasibility trial of screening women with idiopathic recurrent miscarriage for high uterine natural killer cell density and randomizing to prednisolone or placebo when pregnant. Hum Reprod. 2013;28(7):1743–52. https://doi.org/10.1093/humrep/det117.; Yang Y., Ru H., Zhang S. et al. The effect of granulocyte colony-stimulating factor on endometrial receptivity of implantation failure mouse. Reprod Sci. 2025;32(1):200–17. https://doi.org/10.1007/s43032-024-01527-6.; Kalem Z., Namli Kalem M., Bakirarar B. et al. Intrauterine G-CSF administration in recurrent implantation failure (RIF): An Rct. Sci Rep. 2020;10(1):5139. https://doi.org/10.1038/s41598-020-61955-7.; Bumbăcea R.S., Udrea M.R., Ali S., Bojincă V.C. Balancing benefits and risks: a literature review on hypersensitivity reactions to human G-CSF (granulocyte colony-stimulating factor). Int J Mol Sci. 2024;25(9):4807. https://doi.org/10.3390/ijms25094807.; Scarpellini F., Sbracia M. Use of granulocyte colony-stimulating factor for the treatment of unexplained recurrent miscarriage: a randomised controlled trial. Hum Reprod. 2009;24(11):2703–8. https://doi.org/10.1093/humrep/dep240.; Arefi S., Fazeli E., Esfahani M. et al. Granulocyte-colony stimulating factor may improve pregnancy outcome in patients with history of unexplained recurrent implantation failure: an RCT. Int J Reprod Biomed. 2018;16(5):299–304.; Santjohanser C., Knieper C., Franz C. et al. Granulocyte-colony stimulating factor as treatment option in patients with recurrent miscarriage. Arch Immunol Ther Exp (Warsz). 2013;61(2):159–64. https://doi.org/10.1007/s00005-012-0212-z.; https://www.gynecology.su/jour/article/view/2566

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    Academic Journal

    Contributors: This study was performed under the state assignment of D.O. Ott Institute of Obstetrics, Gynecology, and Reproductive Medicine, project number 1021062512052-5-3.2.2., Работа выполнена при финансовой поддержке Министерства науки и высшего образования Российской Федерации (проект №1021062512052-5-3.2.2).

    Source: Vestnik Moskovskogo universiteta. Seriya 16. Biologiya; Том 79, № 3 (2024); 202-210 ; Вестник Московского университета. Серия 16. Биология; Том 79, № 3 (2024); 202-210 ; 0137-0952

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    Relation: https://vestnik-bio-msu.elpub.ru/jour/article/view/1408/692; Milyutina Y.P., Mikhailova V.A., Pyatygina K.M., Demidova E.S., Malygina D.A., Tertychnaia T.E., Arutjunyan A.V., Sokolov D.I., Selkov S.A. Role of caspases in the cytotoxicity of NK-92 cells in various models of coculturing with trophoblasts. Biochemistry (Mosc.). 2019;84(10):1186–1196.; Markova K., Mikhailova V., Milyutina Y., Korenevsky A., Sirotskaya A., Rodygina V., Tyshchuk E., Grebenkina P., Simbirtsev A., Selkov S., Sokolov D. Effects of microvesicles derived from NK cells stimulated with IL-1β on the phenotype and functional activity of endothelial cells. Int. J. Mol. Sci. 2021;22(24):13663.; Del Zotto G., Marcenaro E., Vacca P., Sivori S., Pende D., Della Chiesa M., Moretta F., Ingegnere T., Mingari M.C., Moretta A., Moretta L. Markers and function of human NK cells in normal and pathological conditions. Cytometry B Clin. Cytom. 2017;92(2):100–114.; Михайлова В.А., Белякова К.Л., Сельков С.А., Соколов Д.И. Особенности дифференцировки NK-клеток: CD56dim и CD56bright NK-клетки во время и вне беременности. Мед. иммунол. 2017;19(1):19–26.; Тыщук Е.В., Михайлова В.А., Сельков С.А., Соколов Д.И. Естественные киллеры: происхождение, фенотип, функции. Мед. иммунол. 2021;23(6):1207–1228.; Bazhenov D.O., Mikhailova V.A., Furaeva K.L., Vyaz’mina L.P., Sokolov D.I., Sel’kov S.A. The role of cytokines in maintaining the dynamics of cell-cell interaction between natural killer cells and trophoblast cells. Bull. Exp. Biol. Med. 2022;172(5):622–631.; Bazhenov D., Mikhailova V., Nikolaenkov I., Markova K., Salloum Z., Kogan I., Gzgzyan A., Selkov S., Sokolov D. The uteroplacental contact zone cytokine influence on NK cell cytotoxicity to trophoblasts. Gynecol. Endocrinol. 2020;36(Suppl. 1):1–6.; Mikhailova V.A., Bazhenov D.O., Viazmina L.P., Agnaeva A.O., Bespalova O.N., Sel’kov S.A., Sokolov D.I. Cytotoxic activity of peripheral blood NK cells towards trophoblast cells during pregnancy. Bull. Exp. Biol. Med. 2019;166(4):567–573.; Belyakova K.L., Stepanova O.I., Sheveleva A.R., Mikhailova V.A., Sokolov D.I., Sel’kov S.A. Interaction of NK cells, trophoblast, and endothelial cells during angiogenesis. Bull. Exp. Biol. Med. 2019;167(1):169–176.; Bazhenov D.O., Khokhlova E.V., Viazmina L.P., Furaeva K.N., Mikhailova V.A., Kostin N.A., Selkov S.A., Sokolov D.I. Characteristics of natural killer cell interaction with trophoblast cells during pregnancy. Curr. Mol. Med. 2020;20(3):202–219.; Sokolov D., Gorshkova A., Markova K., Milyutina Y., Pyatygina K., Zementova M., Korenevsky A., Mikhailova V., Selkov S. Natural killer cell derived microvesicles affect the function of trophoblast cells. Membranes. 2023;13(2):213.; Korenevsky A.V., Milyutina Y.P., Bochkovsky S.K., Oshkolova A.A., Bespalova O.N., Selkov S.A., Sokolov D.I. Micropreparative cell lysate fractionation in studying the effect of natural killer cells on phenotype, migration and apoptosis of trophoblast cells in vitro. J. Evol. Biochem. Physiol. 2024;60(4):1385–1398.; Амчиславский Е.И., Соколов Д.И., Сельков С.А., Фрейдлин И.С. Пролиферативная активность эндотелиальных клеток человека линии EA.hy926 и ее модуляция. Цитология. 2005;47(5):393–403.; Nilles J., Weiss J., Theile D. Crystal violet staining is a reliable alternative to bicinchoninic acid assay-based normalization. Biotechniques. 2022;73(3):131–135.; Bass J.J., Wilkinson D.J., Rankin D., Phillips B.E., Szewczyk N.J., Smith K., Atherton P.J. An overview of technical considerations for Western blotting applications to physiological research. Scand. J. Med. Sci. Sports. 2017;27(1):4–25.; Kohler P.O., Bridson W.E. Isolation of hormoneproducing clonal lines of human choriocarcinoma. J. Clin. Endocrinol. Metab. 1971;32(5):683–687.; Gong J.H., Maki G., Klingemann H.G. Characterization of a human cell line (NK-92) with phenotypical and functional characteristics of activated natural killer cells. Leukemia. 1994;8(4):652–658.; Гребенкина П.В., Михайлова В.А., Ошколова А.А., Вершинина С.О., Духинова М.С., Баженов Д.О., Сельков С.А., Соколов Д.И. Децидуальные естественные киллеры и клетки трофобласта: клеточные, гуморальные и молекулярные механизмы взаимодействия. Мед. иммунол. 2022;24(6):1085–1108.; Hanna J., Goldman-Wohl D., Hamani Y., Avraham I., Greenfield C., Natanson-Yaron S., Prus D., Cohen-Daniel L., Arnon T.I., Manaster I., Gazit R., Yutkin V., Benharroch D., Porgador A., Keshet E., Yagel S., Mandelboim O. Decidual NK cells regulate key developmental processes at the human fetal-maternal interface. Nat. Med. 2006;12(9):1065–1074.; Korenevsky A.V., Gert T.N., Berezkina M.E., Sinyavin S.A., Mikhailova V.A., Markova K.L., Simbirtsev A.S., Selkov S.A., Sokolov D.I. Protein fractions of natural killer cell lysates affect the phenotype, proliferation and migration of endothelial cells in vitro. J. Evol. Biochem. Physiol. 2022;58(Suppl. 1):S134–S150.; Korenevsky A.V., Berezkina M.E., Gert T.N., Sinyavin S.A., Selkov S.A., Sokolov D.I. Phenotypic and functional characteristics of endothelial cells: the in vitro effects of protein fractions from the lysate of natural killer-derived microvesicles. Мед. иммунол. 2022;24(3):463–480.; Li Q., Li Z., Luo T., Shi H. Targeting the PI3K/ AKT/mTOR and RAF/MEK/ERK pathways for cancer therapy. Mol. Biomed. 2022;3(1):47.; Iida M., Harari P.M., Wheeler D.L., Toulany M. Targeting AKT/PKB to improve treatment outcomes for solid tumors. Mutat. Res. 2020;819–820:111690.; Guo Y.J., Pan W.W., Liu S.B., Shen Z.F., Xu Y., Hu L.L. ERK/MAPK signalling pathway and tumorigenesis. Exp. Ther. Med. 2020;19(3):1997–2007.; Ahmad J., Ahamad J., Algahtani M.S., Garg A., Shahzad N., Ahmad M.Z., Imam S.S. Nanotechnologymediated delivery of resveratrol as promising strategy to improve therapeutic efficacy in triple negative breast cancer (TNBC): progress and promises. Expert Opin. Drug Deliv. 2024;21(2):229–244.; Cagnol S., Van Obberghen-Schilling E., Chambard J.C. Prolonged activation of ERK1,2 induces FADD-independent caspase 8 activation and cell death. Apoptosis. 2006;11(3):337–346.; Drosopoulos K.G., Roberts M.L., Cermak L., Sasazuki T., Shirasawa S., Andera L., Pintzas A. Transfor mation by oncogenic RAS sensitizes human colon cells to TRAIL-induced apoptosis by up-regulating death receptor 4 and death receptor 5 through a MEK-dependent pathway. J. Biol. Chem. 2005;280(24):22856–22867.; Maik-Rachline G., Hacohen-Lev-Ran A., Seger R. Nuclear ERK: mechanism of translocation, substrates, and role in cancer. Int. J. Mol. Sci. 2019;20(5):1194.; Gao X., Zhang J. Akt signaling dynamics in plasma membrane microdomains visualized by FRET-based reporters. Commun. Integr. Biol. 2009;2(1):32–34.

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    Academic Journal

    Authors: Maltsev, D. V.

    Source: Ukrainian Neurological Journal; № 2—3 (2019); 12—21
    Украинский неврологический журнал; № 2—3 (2019); 12—21
    Український неврологічний журнал; № 2—3 (2019); 12—21

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