Chemically Defined Conditions Mediate an Efficient Induction of Dental Pulp Pluripotent-Like Stem Cells into Hepatocyte-Like Cells

Liver diseases are major causes of morbidity and mortality. Dental pulp pluripotent-like stem cells (DPPSCs) are of a considerable promise in tissue engineering and regenerative medicine as a new source of tissue-specific cells; therefore, this study is aimed at demonstrating their ability to genera...

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Main Authors: Carlos Gil-Recio, Sheyla Montori, Saddam Al Demour, Mera A. Ababneh, Eduard Ferrés-Padró, Carles Marti, Elvira Ferrés-Amat, Miguel Barajas, Ashraf Al Madhoun, Maher Atari
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2021/5212852
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author Carlos Gil-Recio
Sheyla Montori
Saddam Al Demour
Mera A. Ababneh
Eduard Ferrés-Padró
Carles Marti
Elvira Ferrés-Amat
Miguel Barajas
Ashraf Al Madhoun
Maher Atari
author_facet Carlos Gil-Recio
Sheyla Montori
Saddam Al Demour
Mera A. Ababneh
Eduard Ferrés-Padró
Carles Marti
Elvira Ferrés-Amat
Miguel Barajas
Ashraf Al Madhoun
Maher Atari
author_sort Carlos Gil-Recio
collection DOAJ
description Liver diseases are major causes of morbidity and mortality. Dental pulp pluripotent-like stem cells (DPPSCs) are of a considerable promise in tissue engineering and regenerative medicine as a new source of tissue-specific cells; therefore, this study is aimed at demonstrating their ability to generate functional hepatocyte-like cells in vitro. Cells were differentiated on a collagen scaffold in serum-free media supplemented with growth factors and cytokines to recapitulate liver development. At day 5, the differentiated DPPSC cells expressed the endodermal markers FOXA1 and FOXA2. Then, the cells were derived into the hepatic lineage generating hepatocyte-like cells. In addition to the associated morphological changes, the cells expressed the hepatic genes HNF6 and AFP. The terminally differentiated hepatocyte-like cells expressed the liver functional proteins albumin and CYP3A4. In this study, we report an efficient serum-free protocol to differentiate DPPSCs into functional hepatocyte-like cells. Our approach promotes the use of DPPSCs as a new source of adult stem cells for prospective use in liver regenerative medicine.
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issn 1687-9678
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spelling doaj-art-d530ec69fcd04f0fb7f344480fc2b0422025-08-20T02:19:58ZengWileyStem Cells International1687-96782021-01-01202110.1155/2021/5212852Chemically Defined Conditions Mediate an Efficient Induction of Dental Pulp Pluripotent-Like Stem Cells into Hepatocyte-Like CellsCarlos Gil-Recio0Sheyla Montori1Saddam Al Demour2Mera A. Ababneh3Eduard Ferrés-Padró4Carles Marti5Elvira Ferrés-Amat6Miguel Barajas7Ashraf Al Madhoun8Maher Atari9Regenerative Medicine Research InstituteRegenerative Medicine Research InstituteDepartment of Special Surgery/Division of UrologyDepartment of Clinical PharmacyOral and Maxillofacial Surgery DepartmentOral and Maxillofacial Surgery DepartmentPediatric Dentistry ServiceBiochemistry and Molecular Biology DepartmentDepartment of Genetics and BioinformaticsRegenerative Medicine Research InstituteLiver diseases are major causes of morbidity and mortality. Dental pulp pluripotent-like stem cells (DPPSCs) are of a considerable promise in tissue engineering and regenerative medicine as a new source of tissue-specific cells; therefore, this study is aimed at demonstrating their ability to generate functional hepatocyte-like cells in vitro. Cells were differentiated on a collagen scaffold in serum-free media supplemented with growth factors and cytokines to recapitulate liver development. At day 5, the differentiated DPPSC cells expressed the endodermal markers FOXA1 and FOXA2. Then, the cells were derived into the hepatic lineage generating hepatocyte-like cells. In addition to the associated morphological changes, the cells expressed the hepatic genes HNF6 and AFP. The terminally differentiated hepatocyte-like cells expressed the liver functional proteins albumin and CYP3A4. In this study, we report an efficient serum-free protocol to differentiate DPPSCs into functional hepatocyte-like cells. Our approach promotes the use of DPPSCs as a new source of adult stem cells for prospective use in liver regenerative medicine.http://dx.doi.org/10.1155/2021/5212852
spellingShingle Carlos Gil-Recio
Sheyla Montori
Saddam Al Demour
Mera A. Ababneh
Eduard Ferrés-Padró
Carles Marti
Elvira Ferrés-Amat
Miguel Barajas
Ashraf Al Madhoun
Maher Atari
Chemically Defined Conditions Mediate an Efficient Induction of Dental Pulp Pluripotent-Like Stem Cells into Hepatocyte-Like Cells
Stem Cells International
title Chemically Defined Conditions Mediate an Efficient Induction of Dental Pulp Pluripotent-Like Stem Cells into Hepatocyte-Like Cells
title_full Chemically Defined Conditions Mediate an Efficient Induction of Dental Pulp Pluripotent-Like Stem Cells into Hepatocyte-Like Cells
title_fullStr Chemically Defined Conditions Mediate an Efficient Induction of Dental Pulp Pluripotent-Like Stem Cells into Hepatocyte-Like Cells
title_full_unstemmed Chemically Defined Conditions Mediate an Efficient Induction of Dental Pulp Pluripotent-Like Stem Cells into Hepatocyte-Like Cells
title_short Chemically Defined Conditions Mediate an Efficient Induction of Dental Pulp Pluripotent-Like Stem Cells into Hepatocyte-Like Cells
title_sort chemically defined conditions mediate an efficient induction of dental pulp pluripotent like stem cells into hepatocyte like cells
url http://dx.doi.org/10.1155/2021/5212852
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