Modeling human infertility with pluripotent stem cells

被引:23
作者
Chen, Di [1 ,3 ,5 ]
Gell, Joanna J. [2 ,3 ,4 ]
Tao, Yu [1 ,3 ,5 ]
Sosa, Enrique [1 ,3 ,5 ]
Clark, Amander T. [1 ,3 ,5 ]
机构
[1] Dept Mol Cell & Dev Biol, Los Angeles, CA 90095 USA
[2] Dept Pediat, Div Hematol Oncol, Los Angeles, CA 90095 USA
[3] Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, Los Angeles, CA 90095 USA
[4] David Geffen Sch Med, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Los Angeles, CA 90095 USA
关键词
PRIMORDIAL GERM-CELLS; SPECIFICATION; DIFFERENTIATION; FATE; LINEAGE; GENE; INDUCTION; DYNAMICS; MONKEYS;
D O I
10.1016/j.scr.2017.04.005
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Human fertility is dependent upon the correct establishment and differentiation of the germline. This is because no other cell type in the body is capable of passing a genome and epigenome from parent to child. Terminally differentiated germline cells in the adult testis and ovary are called gametes. However the initial specification of germline cells occurs in the embryo around the time of gastrulation. Most of our knowledge regarding the cell and molecular events that govern human germline specification involves extrapolating scientific principles from model organisms most notably the mouse. However recent work using next generation sequencing gene editing and differentiation of germline cells from pluripotent stem cells has revealed that the core molecular mechanisms that regulate human germline development are different from rodents. Here we will discuss the major molecular pathways required for human germline differentiation and how pluripotent stem cells have revolutionized our ability to study the earliest steps in human embryonic lineage specification in order to understand human fertility. (C) 2017 The Authors. Published by Elsevier BV
引用
收藏
页码:187 / 192
页数:6
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