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Evidence of Adult Features and Functions of Hepatocytes Differentiated from Human Induced Pluripotent Stem Cells and Self-Organized as Organoids.

Authors :
Messina A
Luce E
Benzoubir N
Pasqua M
Pereira U
Humbert L
Eguether T
Rainteau D
Duclos-Vallée JC
Legallais C
Dubart-Kupperschmitt A
Source :
Cells [Cells] 2022 Feb 04; Vol. 11 (3). Date of Electronic Publication: 2022 Feb 04.
Publication Year :
2022

Abstract

Background: Human-induced pluripotent stem cell-derived hepatocytes (iHeps) have been shown to have considerable potential in liver diseases, toxicity, and pharmacological studies. However, there is a growing need to obtain iHeps that are truly similar to primary adult hepatocytes in terms of morphological features and functions. We generated such human iHeps, self-assembled as organoids (iHep-Orgs).<br />Methods: iPSC-derived hepatoblasts were self-assembled into spheroids and differentiated into mature hepatocytes modulating final step of differentiation.<br />Results: In about four weeks of culture, the albumin secretion levels and the complete disappearance of α-fetoprotein from iHep-Orgs suggested the acquisition of a greater degree of maturation than those previously reported. The expression of apical transporters and bile acid secretion evidenced the acquisition of complex hepatocyte polarity as well as the development of a functional and well-defined bile canalicular network confirmed by computational analysis. Activities recorded for CYP450, UGT1A1, and alcohol dehydrogenase, response to hormonal stimulation, and glucose metabolism were also remarkable. Finally, iHep-Orgs displayed a considerable ability to detoxify pathological concentrations of lactate and ammonia.<br />Conclusions: With features similar to those of primary adult hepatocytes, the iHep-Orgs thus produced could be considered as a valuable tool for the development and optimization of preclinical and clinical applications.

Details

Language :
English
ISSN :
2073-4409
Volume :
11
Issue :
3
Database :
MEDLINE
Journal :
Cells
Publication Type :
Academic Journal
Accession number :
35159346
Full Text :
https://doi.org/10.3390/cells11030537