Chicken Interspecies Chimerism Unveils Human Pluripotency

Stem Cell Reports. 2021 Jan 12;16(1):39-55. doi: 10.1016/j.stemcr.2020.11.014. Epub 2020 Dec 23.

Abstract

Human pluripotent stem cells (hPSCs) are commonly kept in a primed state but also able to acquire a more immature naive state under specific conditions in vitro. Acquisition of naive state changes several properties of hPSCs and might affect their contribution to embryonic development in vivo. However, the lack of an appropriate animal test system has made it difficult to assess potential differences for chimera formation between naive and primed hPSCs. Here, we report that the developing chicken embryo is a permissive host for hPSCs, allowing analysis of the pluripotency potential of hPSCs. Transplantation of naive-like and primed hPSCs at matched developmental stages resulted in robust chimerism. Importantly, the ability of naive-like but not of primed hPSCs to form chimera was substantially reduced when injected at non-matched developmental stages. We propose that contribution to chick embryogenesis is an informative and versatile test to identify different pluripotent states of hPSCs.

Keywords: chick embryo; chimera formation; interspecies chimera formation; naive and primed human pluripotent states; pluripotency.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Cell Lineage
  • Chick Embryo / cytology
  • Chick Embryo / metabolism*
  • Chickens
  • Chimerism / veterinary*
  • Embryonic Development
  • Gene Editing
  • Humans
  • LIM-Homeodomain Proteins / genetics
  • Pluripotent Stem Cells / cytology
  • Pluripotent Stem Cells / metabolism
  • Pluripotent Stem Cells / transplantation*
  • SOXB1 Transcription Factors / genetics
  • SOXB1 Transcription Factors / metabolism
  • Transcription Factors / genetics
  • Tubulin / genetics
  • Tubulin / metabolism

Substances

  • LIM-Homeodomain Proteins
  • SOXB1 Transcription Factors
  • Transcription Factors
  • Tubulin
  • insulin gene enhancer binding protein Isl-1