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The effect of liver donors' age, gender and metabolic state on pancreatic lineage activation

  • Ioan Valentin Matei
  • , Irit Meivar-Levy
  • , Daniela Lixandru
  • , Simona Olimpia Dima
  • , Ioana Raluca Florea
  • , Veronica Madalina Aspritoiu
  • , Radu Albulescu
  • , Irinel Popescu
  • , Sarah Ferber*
  • *Corresponding author for this work
  • University of Bucharest
  • The Sheba Regenerative Medicine, Stem Cell and Tissue Engineering Center, Sheba Medical Center,
  • Orgenesis Ltd, Ness Ziona, Israel.
  • Carol Davila University of Medicine and Pharmacy Bucharest, Romania
  • Fundeni Clinical Institute, Bucharest, Romania.
  • Victor Babes National Institute of Pathology, Bucharest, Romania
  • Tel Aviv University

Research output: Contribution to journalArticle (journal)peer-review

Abstract

Autologous cells replacement therapy by liver to pancreas transdifferentiation (TD) allows diabetic patients to be also the donors of their own therapeutic tissue. Aim: To analyze whether the efficiency of the process is affected by liver donors' heterogeneity with regard to age, gender and the metabolic state. Materials & methods: TD of liver cells derived from nondiabetic and diabetic donors at different ages was characterized at molecular and cellular levels, in vitro. Results: Neither liver cells proliferation nor the propagated cells TD efficiency directly correlate with the age (3-60 years), gender or the metabolic state of the donors. Conclusion: Human liver cells derived from a wide array of ages and metabolic states can be used for autologous cells therapies for diabetics.
Original languageEnglish
Pages (from-to)19-31
Number of pages13
JournalRegenerative Medicine
Volume16
Issue number1
DOIs
Publication statusPublished - 2 Feb 2021
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • adult cell reprogramming
  • cell replacement therapy
  • diabetes
  • liver
  • pancreatic transcription factors
  • transdifferentiation

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