Integrative protocols for an in vitro generation of pancreatic progenitors from human dental pulp stem cells.


Journal

Biochemical and biophysical research communications
ISSN: 1090-2104
Titre abrégé: Biochem Biophys Res Commun
Pays: United States
ID NLM: 0372516

Informations de publication

Date de publication:
10 09 2020
Historique:
received: 11 05 2020
accepted: 26 06 2020
entrez: 24 8 2020
pubmed: 24 8 2020
medline: 27 2 2021
Statut: ppublish

Résumé

Efficiency of the induction protocol is crucial for the generation of insulin-producing cells (IPCs) from human dental pulp stem cells (hDPSCs). Here, we established the integrative induction protocol by merging genetic manipulation technique with our previous published 3-step induction protocol aiming to enhance the pancreatic progenitor commitment and production yield. We found that the overexpression of PDX1 following with 3-step induction protocol were able to generate the 3-dimensional (3D) colony structure of pancreatic progenitors (PPs) with the beneficial trends of pancreatic endoderm commitment and production yield, while other protocols using the prolong maintenance of PDX1-overexpressed hDPSCs and the PDX1 overexpression after definitive endoderm induction were unable to generate and sustain the 3D structure of the colonies. Further Notch signaling manipulation by DAPT treatment showed lesser degree of positive effects on progenitor commitment and production yield. Although the generated PPs from the integrative protocol expressed pancreatic mRNA markers along with pro-insulin and insulin proteins, they still contained the defective glucose-responsive C-peptide secretion. Only basal secreted C-peptide level was observed. In summary, the integrative induction protocol potentially enhanced the PP generation with high colony production yield and could serve as an efficient platform for further hDPSC-derived IPC production and maturation.

Identifiants

pubmed: 32828290
pii: S0006-291X(20)31364-4
doi: 10.1016/j.bbrc.2020.06.145
pii:
doi:

Substances chimiques

C-Peptide 0
Homeodomain Proteins 0
Trans-Activators 0
pancreatic and duodenal homeobox 1 protein 0
Glucose IY9XDZ35W2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

222-229

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors have no financial support or personal relationship with individuals or organizations that could inappropriately influence or bias the content of this paper.

Auteurs

Chenphop Sawangmake (C)

Department of Pharmacology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand; Veterinary Clinical Stem Cell and Bioengineering Research Unit, Veterinary Stem Cell and Bioengineering Innovation Center (VSCBIC), Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand. Electronic address: chenphop.s@chula.ac.th.

Watchareewan Rodprasert (W)

Veterinary Clinical Stem Cell and Bioengineering Research Unit, Veterinary Stem Cell and Bioengineering Innovation Center (VSCBIC), Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand. Electronic address: watchareewan.r@gmail.com.

Thanaphum Osathanon (T)

Department of Anatomy, Center of Excellence for Regenerative Dentistry, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand. Electronic address: thanaphum.o@chula.ac.th.

Prasit Pavasant (P)

Department of Anatomy, Center of Excellence for Regenerative Dentistry, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand. Electronic address: prasit215@gmail.com.

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Classifications MeSH