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Multipotent Fetal Stem Cells in Reproductive Biology Research

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Publisher Biomed Central
Date 2023 Jun 7
PMID 37287077
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Abstract

Due to the limited accessibility of the in vivo situation, the scarcity of the human tissue, legal constraints, and ethical considerations, the underlying molecular mechanisms of disorders, such as preeclampsia, the pathological consequences of fetomaternal microchimerism, or infertility, are still not fully understood. And although substantial progress has already been made, the therapeutic strategies for reproductive system diseases are still facing limitations. In the recent years, it became more and more evident that stem cells are powerful tools for basic research in human reproduction and stem cell-based approaches moved into the center of endeavors to establish new clinical concepts. Multipotent fetal stem cells derived from the amniotic fluid, amniotic membrane, chorion leave, Wharton´s jelly, or placenta came to the fore because they are easy to acquire, are not associated with ethical concerns or covered by strict legal restrictions, and can be banked for autologous utilization later in life. Compared to adult stem cells, they exhibit a significantly higher differentiation potential and are much easier to propagate in vitro. Compared to pluripotent stem cells, they harbor less mutations, are not tumorigenic, and exhibit low immunogenicity. Studies on multipotent fetal stem cells can be invaluable to gain knowledge on the development of dysfunctional fetal cell types, to characterize the fetal stem cells migrating into the body of a pregnant woman in the context of fetomaternal microchimerism, and to obtain a more comprehensive picture of germ cell development in the course of in vitro differentiation experiments. The in vivo transplantation of fetal stem cells or their paracrine factors can mediate therapeutic effects in preeclampsia and can restore reproductive organ functions. Together with the use of fetal stem cell-derived gametes, such strategies could once help individuals, who do not develop functional gametes, to conceive genetically related children. Although there is still a long way to go, these developments regarding the usage of multipotent fetal stem cells in the clinic should continuously be accompanied by a wide and detailed ethical discussion.

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References
1.
Moraghebi R, Kirkeby A, Chaves P, Ronn R, Sitnicka E, Parmar M . Term amniotic fluid: an unexploited reserve of mesenchymal stromal cells for reprogramming and potential cell therapy applications. Stem Cell Res Ther. 2017; 8(1):190. PMC: 5574087. DOI: 10.1186/s13287-017-0582-6. View

2.
Lankford L, Selby T, Becker J, Ryzhuk V, Long C, Farmer D . Early gestation chorionic villi-derived stromal cells for fetal tissue engineering. World J Stem Cells. 2015; 7(1):195-207. PMC: 4300931. DOI: 10.4252/wjsc.v7.i1.195. View

3.
Yi X, Chen F, Liu F, Peng Q, Li Y, Li S . Comparative separation methods and biological characteristics of human placental and umbilical cord mesenchymal stem cells in serum-free culture conditions. Stem Cell Res Ther. 2020; 11(1):183. PMC: 7238656. DOI: 10.1186/s13287-020-01690-y. View

4.
Geng Z, Chen H, Zou G, Yuan L, Liu P, Li B . Human Amniotic Fluid Mesenchymal Stem Cell-Derived Exosomes Inhibit Apoptosis in Ovarian Granulosa Cell via miR-369-3p/YAF2/PDCD5/p53 Pathway. Oxid Med Cell Longev. 2022; 2022:3695848. PMC: 9346541. DOI: 10.1155/2022/3695848. View

5.
Taylor P, McElmurry R, Lees C, Harrison D, Blazar B . Allogenic fetal liver cells have a distinct competitive engraftment advantage over adult bone marrow cells when infused into fetal as compared with adult severe combined immunodeficient recipients. Blood. 2002; 99(5):1870-2. DOI: 10.1182/blood.v99.5.1870. View