Increased Migration Ability of Adenomyosis-Derived Endometrial Mesenchymal Stem Cells

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Endometrial mesenchymal stem cells from adenomyosis patients exhibit significantly increased migration rates in a wound healing assay compared to healthy controls, despite smaller cell size.

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The paper compares human endometrial mesenchymal stem cells (eMSCs) isolated from menstrual blood of a healthy donor versus a single donor with adenomyosis, assessing morphological features and migratory behavior. Using a wound-healing assay with live-cell microscopy, the authors report that adenomyosis-derived eMSCs migrated faster and displayed higher wound-healing rates than normal eMSCs, while also being smaller in area and perimeter; polarization-related morphometrics did not differ. A major caveat is that migration differences depended on culture conditions, since in serum-free medium eMSC-A migrated more slowly than normal cells. This paper is centrally about endometriosis/adenomyosis — specifically adenomyosis-derived endometrial mesenchymal stem cells with increased migration potential in standard conditions.

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Abstract

Adenomyosis is a form of endometriosis—a gynecological disease associated with abnormal functional activity of endometrial cells. Endometrial stem cells can play a key role in the pathogenesis of this disease. Despite the numerous studies that have been conducted of cultures of endometrial mesenchymal stem cells (eMSCs) obtained from patients with adenomyosis, information on their phenotypic and functional properties is very contradictory. In this work, a comparative study of morphological and migratory characteristics of human endometrial mesenchymal stem cells isolated from the menstrual blood of healthy donors (eMSCs) and a donor with adenomyosis (eMSCs-A) was performed. eMSC migration was evaluated by the method of “wound healing” using live-cell microscopy. It was established that the rate of wound healing of eMSCs-A is significantly higher compared to normal cells, which indicates an increased migration potential of eMSCs-A in adenomyosis. However, when transferring cells to a serum-free medium, eMSC-A migrated more slowly than normal cells. As a result of the assessment of morphological characteristics, it was found that eMSCs-A are smaller (in area and perimeter) than normal eMSCs, while the remaining morphometric parameters reflecting cell polarization did not differ. The data obtained allow the use of eMSCs in culture as a model for elucidating the membrane and intracellular mechanisms that underlie changes in cellular mechanics, motility, and invasive activity in various pathologies, including adenomyosis.
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Abstract

Adenomyosis is a form of endometriosis—a gynecological disease associated with abnormal functional activity of endometrial cells. Endometrial stem cells can play a key role in the pathogenesis of this disease. Despite the numerous studies that have been conducted of cultures of endometrial mesenchymal stem cells (eMSCs) obtained from patients with adenomyosis, information on their phenotypic and functional properties is very contradictory. In this work, a comparative study of morphological and migratory characteristics of human endometrial mesenchymal stem cells isolated from the menstrual blood of healthy donors (eMSCs) and a donor with adenomyosis (eMSCs-A) was performed. eMSC migration was evaluated by the method of “wound healing” using live-cell microscopy. It was established that the rate of wound healing of eMSCs-A is significantly higher compared to normal cells, which indicates an increased migration potential of eMSCs-A in adenomyosis. However, when transferring cells to a serum-free medium, eMSC-A migrated more slowly than normal cells. As a result of the assessment of morphological characteristics, it was found that eMSCs-A are smaller (in area and perimeter) than normal eMSCs, while the remaining morphometric parameters reflecting cell polarization did not differ. The data obtained allow the use of eMSCs in culture as a model for elucidating the membrane and intracellular mechanisms that underlie changes in cellular mechanics, motility, and invasive activity in various pathologies, including adenomyosis. Similar content being viewed by others

References

Banu, S.K., Lee, J.H., Starzinski-Powitz, A., and Arosh, J.A., Gene expression profiles and functional characterization of human immortalized endometriotic epithelial and stromal cells, Fertil. Steril., 2008, vol. 90, pp. 972–987. Brink, H.E., Stalling, S.S., and Nicoll, S.B., Influence of serum on adult and fetal dermal fibroblast migration, adhesion, and collagen expression, In Vitro Cell. Dev. Biol. Anim., 2005, vol. 41, pp. 252–257. Chen, Y.-J., Li, H-Y., Chang, Y.-L., Yuan, C.-C., Tai, L.-K., Lu, K.H., Chang, C.-M., and Chiou, S.-H., Suppression of migratory/invasive ability and induction of apoptosis in adenomyosis-derived mesenchymal stem cells by cyclooxygenase-2 inhibitors, Fertil. Steril., 2010, vol. 94, pp. 1972–1979. Chen, L., Qu, J., and Xiang, C., The multi-functional roles of menstrual blood-derived stem cells in regenerative medicine, Stem Cell Res. Ther., 2019, vol. 10, no. 1. https://doi.org/10.1186/s13287-018-1105-9 Chubinskiy-Nadezhdin, V.I., Efremova, T.N., Khaitlina, S.Y., and Morachevskaya, E.A., Functional impact of cholesterol sequestration on actin cytoskeleton in normal and transformed fibroblasts, Cell Biol. Int., 2013, vol. 37, pp. 617–623. Dhesi, A.S. and Morelli, S.S., Endometriosis: a role for stem cells, Womens Health, 2015, vol. 11, pp. 35–49. Gottipamula, S., Ashwin, K.M., Muttigi, M.S., Kannan, S., Kolkundkar, U., and Seetharam, R.N., Isolation, expansion and characterization of bone marrow-derived mesenchymal stromal cells in serum-free conditions, Cell Tissue Res., 2014, vol. 356, pp. 123–135. Hegera, J.I., Froehlicha, K., Pastuscheka, J., Schmidta, A., Baera, C., Mrowkab, R., Backschc, C., Schleußnera, E., Markerta, U.R., and Schmidta, A., Human serum alters cell culture behavior and improves spheroid formationin comparison to fetal bovine serum, Exp. Cell Res., 2018, vol. 365, pp. 57–65. Kao, A.P., Wang, K.H., Chang, C.C., Lee, J.N., Long, C.Y., Chen, H.S., Tsai, C.F., Hsieh, T.H., and Tsai, E.M., Comparative study of human eutopic and ectopic endometrial mesenchymal stem cells and the development of an in vivo endometriotic invasion model, Fertil. Steril., 2011a, vol. 95, pp. 1308–1315. Kao, A.P., Wang, K.H., Long, C.Y., Chai, C.Y., Tsai, C.F., Hsieh, T.H., Hsu, C.Y., Chang, C.C., Lee, J.N., and Tsai, E.M., Interleukin-1beta induces cyclooxygenase-2 expression and promotes the invasive ability of human mesenchymal stem cells derived from ovarian endometrioma, Fertil. Steril., 2011b, vol. 96, pp. 678–684. Lloyd, A.C., The regulation of cell size, Cell, 2013, vol. 154, pp. 1194–1205. Nikoo, S., Ebtekar, M., Jeddi-Tehrani, M., Shervin, A., Bozorgmehr, M., Vafaei, S, Kazemnejad, S, and Zarnani, A.-H., Menstrual blood-derived stromal stem cells from women with and without endometriosis reveal different phenotypic and functional characteristics, Mol. Hum. Reprod., 2014, vol. 20, pp. 905–918. Sasson, I.E. and Taylor, H.S., Stem cells and the pathogenesis of endometriosis, Ann. N.Y. Acad. Sci., 2008, vol. 1127, pp. 106–115. Shilina, M.A., Domnina, A.P., Kozhukharova, I.V., Zenin, V.V., Anisimov, S.V., Nikolsky, N.N., and Grinchuk, T.M., Establishment and characterization of a novel human endometrial mesenchymal stem cell line from a patient with adenomyosis, Cell Tissue Biol., 2016, vol. 10, no. 1, pp. 10–17. Solmesky, L., Lefler, S., Jacob-Hirsch, J., Bulvik, S., Rechavi, G., and Weil, M., Serum free cultured bone marrow mesenchymal stem cells as a platform to characterize the effects of specific molecules, PLoS One, 2010, vol. 5, no. 9. e12689. https://doi.org/10.1371/journal.pone.0012689 Yoshida, K., Nakashima, A., Doi, S, Ueno, T., Okubo, T., Kawano, K.-I., Kanawa, M., Kato, Y., Higashi, Y., and Masaki, T., Serum-free medium enhances the immunosuppressive and antifibrotic abilities of mesenchymal stem cells utilized in experimental renal fibrosis, Stem Cells Transl. Med., 2018, vol. 7, pp. 893–905. Zemelko, V.I., Grinchuk, T.M., Domnina, A.P., Artsybasheva, I.V., Zenin, V.V., Kirsanov, A.A., Bichevaya, N.K., Korsak, V.S., and Nikolsky, N.N., Multipotent mesenchymal stem cells of desquamated endometrium: isolation, characterization, and application as a feeder layer for maintenance of human embryonic stem cells, Cell Tissue Biol., 2012, vol. 6, no. 1, pp. 1–11. Funding This study was financed by the Russian Science Foundation, project no. 18-15-00106. Author information Authors and Affiliations Corresponding author Ethics declarations The authors declare that they have no conflict of interest.The authors did not conduct experiments involving animals or human beings. Cell lines obtained and characterized previously (Shilina et al., 2015) were used. Additional information Abbreviations: eMSC—endometrial mesenchymal stem cell isolated from the menstrual blood of healthy donors, eMSC-A—eMSC isolated from menstrual blood of a donor with adenomyosis, FBS—fetal bovine serum. Rights and permissions About this article Cite this article Sudarikova, A.V., Shilina, M.A., Chubinskiy-Nadezhdin, V.I. et al. Increased Migration Ability of Adenomyosis-Derived Endometrial Mesenchymal Stem Cells. Cell Tiss. Biol. 14, 190–195 (2020). https://doi.org/10.1134/S1990519X20030062 Received: Revised: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1134/S1990519X20030062

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