4.8 Article

Establishment of Trophoblast-Like Tissue Model from Human Pluripotent Stem Cells in Three-Dimensional Culture System

期刊

ADVANCED SCIENCE
卷 9, 期 3, 页码 -

出版社

WILEY
DOI: 10.1002/advs.202100031

关键词

human pluripotent stem cells; matrices; placenta development; three-dimensional cultures; trophoblast tissues

资金

  1. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB29050301, XDA16020900, XDB32030200]
  2. National Key R&D Program of China [2017YFB0405404]
  3. National Nature Science Foundation of China [31971373, 81803492]
  4. Innovation Program of Science and Research from the DICP, CAS [DICPI201934]
  5. Yunnan Key Research and Development Program [202003AD150009]

向作者/读者索取更多资源

The study reports the generation of a novel trophoblast-like tissue model from human pluripotent stem cells, which can reflect key features of early human placental development.
The placenta has a lifelong impact on the health of both the mother and fetus. Despite its significance, human early placental development is poorly understood due to the limited models. The models that can reflect the key features of early human placental development, especially at early gestation, are still lacking. Here, the authors report the generation of trophoblast-like tissue model from human pluripotent stem cells (hPSCs) in three-dimensional (3D) cultures. hPSCs efficiently self-organize into blastocoel-like cavities under defined conditions, which produce different trophoblast subtypes, including cytotrophoblasts (CTBs), syncytiotrophoblasts (STBs), and invasive extravillous trophoblasts (EVTs). The 3D cultures can exhibit microvilli structure and secrete human placenta-specific hormone. Single-cell RNA sequencing analysis further identifies the presence of major cell types of trophoblast-like tissue as existing in vivo. The results reveal the feasibility to establish 3D trophoblast-like tissue model from hPSCs in vitro, which is not obtained by monolayer culture. This new model system can not only facilitate to dissect the underlying mechanisms of early human placental development, but also imply its potential for study in developmental biology and gestational disorders.

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