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

Author:

Matei Ioan V1ORCID,Meivar-Levy Irit123ORCID,Lixandru Daniela45,Dima Simona14,Florea Ioana R146,Ilie Veronica M146,Albulescu Radu178,Popescu Irinel14,Ferber Sarah1239

Affiliation:

1. Dia-Cure, Acad. Nicolae Cajal Institute of Medical Scientific Research, Titu Maiorescu University Bucharest, 040441, Romania

2. The Sheba Regenerative Medicine, Stem Cell & Tissue Engineering Center, Sheba Medical Center, Tel-Hashomer, 5262100, Israel

3. Orgenesis Ltd, Ness Ziona, 7414002, Israel

4. Fundeni Clinical Institute, Bucharest, 022328, Romania

5. University of Medicine & Pharmacy ‘Carol Davila’, Bucharest, 050474, Romania

6. University of Bucharest, Faculty of Biology, Bucharest, 050663, Romania

7. National Institute for Chemical Pharmaceutical R&D, Bucharest,031299, Romania

8. Victor Babes National Institute of Pathology, Bucharest, 050096, Romania

9. ,Department of Human Genetics, Tel Aviv University, Sackler School of Medicine, Tel Aviv, 6997801, Israel

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.

Funder

The Israel Science Foundation

Dia Cure

Publisher

Future Medicine Ltd

Subject

Embryology,Biomedical Engineering

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