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Maturity and age influence chief cell ability to transdifferentiate into metaplasia.

Victoria G WeisChristine P PetersenJared A WeisAnne R MeyerEunyoung ChoiJason C MillsJames R Goldenring
Published in: American journal of physiology. Gastrointestinal and liver physiology (2016)
Previous investigations have indicated that spasmolytic polypeptide-expressing metaplasia (SPEM) in the stomach arises from transdifferentiation of chief cells. Nevertheless, the intrinsic properties of chief cells that influence transdifferentiation have been largely unknown. We now report that the ability to transdifferentiate into SPEM is impaired in chief cells that lack full functional maturation, and as chief cells age, they lose their ability to transdifferentiate. Thus chief cell plasticity is dependent on both cell age and maturation.
Keyphrases
  • induced apoptosis
  • cell cycle arrest
  • single cell
  • cell therapy
  • cell death
  • signaling pathway
  • stem cells
  • bone marrow
  • wild type