Human mesenchymal stem cells in spheroids improve fertility in model animals with damaged endometrium

被引:69
作者
Domnina, Alisa [1 ]
Novikova, Polina [2 ]
Obidina, Julia [1 ]
Fridlyanskaya, Irina [1 ]
Alekseenko, Larisa [1 ]
Kozhukharova, Irina [1 ]
Lyublinskaya, Olga [1 ]
Zenin, Valeriy [1 ]
Nikolsky, Nikolay [1 ]
机构
[1] Russian Acad Sci, Inst Cytol, St Petersburg, Russia
[2] St Petersburg State Univ, Fac Med, St Petersburg, Russia
来源
STEM CELL RESEARCH & THERAPY | 2018年 / 9卷
基金
俄罗斯科学基金会;
关键词
Endometrial mesenchymal stem cells; Cell spheroids; Asherman's syndrome; Animal model; STROMAL CELLS; ASHERMANS-SYNDROME; CD146; EXPRESSION; SURVIVAL; REGENERATION; THERAPY;
D O I
10.1186/s13287-018-0801-9
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background: Asherman's syndrome (AS) is one of the gynecological disorders caused by the destruction of the endometrium. For some cases of AS available surgical methods and hormonal therapy are ineffective. Stem cell transplantation may offer a potential alternative for AS cure. Methods: Human endometrial mesenchymal stem cells (eMSC) organized in spheroids were transplanted in rats with damaged endometrium modeled on AS. Treatment response was defined as pregnancy outcome and litter size. Results: Application of eMSC in spheroids significantly improved the rat fertility with the AS model. eMSC organized in spheroids retain all properties of eMSC in monolayer: growth characteristics, expression of CD markers, and differentiation potential. Synthesis of angiogenic and anti-inflammatory factors drastically increased in eMSC assembled into spheroids. Conclusions: Human endometrial mesenchymal stem cells (eMSC) can be successfully applied for Asherman's syndrome (AS) treatment in the rat model. eMSC organized in spheroids were more therapeutically effective than the cells in monolayer. After transplantation of eMSC in spheroids the pregnancy outcome and litter size in rats with AS was higher than in rats that received autologous rat bone marrow cells. It suggests the therapeutic plausibility of heterologous eMSC in case of failure to use autologous cells.
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页数:12
相关论文
共 53 条
  • [1] Bone Marrow-Derived Stem Cell (BMDSC) Transplantation Improves Fertility in a Murine Model of Asherman's Syndrome
    Alawadhi, Feryal
    Du, Hongling
    Cakmak, Hakan
    Taylor, Hugh S.
    [J]. PLOS ONE, 2014, 9 (05):
  • [2] Heat shock induces apoptosis in human embryonic stem cells but a premature senescence phenotype in their differentiated progeny
    Alekseenko, Larisa L.
    Zemelko, Victoria I.
    Zenin, Valery V.
    Pugovkina, Nataly A.
    Kozhukharova, Irina V.
    Kovaleva, Zoya V.
    Grinchuk, Tatiana M.
    Fridlyanskaya, Irina I.
    Nikolsky, Nikolay N.
    [J]. CELL CYCLE, 2012, 11 (17) : 3260 - 3269
  • [3] Bahrambeigi Vahid, 2012, Adv Biomed Res, V1, P8, DOI 10.4103/2277-9175.94431
  • [4] Spheroid Culture of Mesenchymal Stem Cells
    Cesarz, Zoe
    Tamama, Kenichi
    [J]. STEM CELLS INTERNATIONAL, 2016, 2016
  • [5] Lifetime expression of stem cell markers in the uterine endometrium
    Cho, NH
    Park, YK
    Kim, YT
    Yang, H
    Kim, SK
    [J]. FERTILITY AND STERILITY, 2004, 81 (02) : 403 - 407
  • [6] ClinicalTrials. gov, 2000, NAT LIB MED
  • [7] Isolation of amniotic stem cell lines with potential for therapy
    De Coppi, Paolo
    Bartsch, Georg, Jr.
    Siddiqui, M. Minhaj
    Xu, Tao
    Santos, Cesar C.
    Perin, Laura
    Mostoslavsky, Gustavo
    Serre, Angeline C.
    Snyder, Evan Y.
    Yoo, James J.
    Furth, Mark E.
    Soker, Shay
    Atala, Anthony
    [J]. NATURE BIOTECHNOLOGY, 2007, 25 (01) : 100 - 106
  • [8] Review of Intrauterine Adhesions
    Deans, Rebecca
    Abbott, Jason
    [J]. JOURNAL OF MINIMALLY INVASIVE GYNECOLOGY, 2010, 17 (05) : 555 - 569
  • [9] DMOWSKI WP, 1969, OBSTET GYNECOL, V34, P288
  • [10] Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement
    Dominici, M.
    Le Blanc, K.
    Mueller, I.
    Slaper-Cortenbach, I.
    Marini, F. C.
    Krause, D. S.
    Deans, R. J.
    Keating, A.
    Prockop, D. J.
    Horwitz, E. M.
    [J]. CYTOTHERAPY, 2006, 8 (04) : 315 - 317