Reprogramming—Evolving Path to Functional Surrogate β-Cells

Numerous cell sources are being explored to replenish functional β-cell mass since the proof-of -concept for cell therapy of diabetes was laid down by transplantation of islets. Many of these cell sources have been shown to possess a degree of plasticity permitting differentiation along new lineages...

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Main Authors: Eric Kalo, Scott Read, Golo Ahlenstiel
Format: Article
Language:English
Published: MDPI AG 2022-09-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/11/18/2813
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author Eric Kalo
Scott Read
Golo Ahlenstiel
author_facet Eric Kalo
Scott Read
Golo Ahlenstiel
author_sort Eric Kalo
collection DOAJ
description Numerous cell sources are being explored to replenish functional β-cell mass since the proof-of -concept for cell therapy of diabetes was laid down by transplantation of islets. Many of these cell sources have been shown to possess a degree of plasticity permitting differentiation along new lineages into insulin-secreting β-cells. In this review, we explore emerging reprograming pathways that aim to generate bone fide insulin producing cells. We focus on small molecules and key transcriptional regulators that orchestrate phenotypic conversion and maintenance of engineered cells.
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spelling doaj.art-a59be7acc37f404aba15b562bf6f2b7c2023-11-23T15:32:40ZengMDPI AGCells2073-44092022-09-011118281310.3390/cells11182813Reprogramming—Evolving Path to Functional Surrogate β-CellsEric Kalo0Scott Read1Golo Ahlenstiel2Blacktown Clinical School and Research Centre, School of Medicine, Western Sydney University, Blacktown, NSW 2148, AustraliaBlacktown Clinical School and Research Centre, School of Medicine, Western Sydney University, Blacktown, NSW 2148, AustraliaBlacktown Clinical School and Research Centre, School of Medicine, Western Sydney University, Blacktown, NSW 2148, AustraliaNumerous cell sources are being explored to replenish functional β-cell mass since the proof-of -concept for cell therapy of diabetes was laid down by transplantation of islets. Many of these cell sources have been shown to possess a degree of plasticity permitting differentiation along new lineages into insulin-secreting β-cells. In this review, we explore emerging reprograming pathways that aim to generate bone fide insulin producing cells. We focus on small molecules and key transcriptional regulators that orchestrate phenotypic conversion and maintenance of engineered cells.https://www.mdpi.com/2073-4409/11/18/2813β-celldiabetes mellituscell sourcesreprogramminginsulin
spellingShingle Eric Kalo
Scott Read
Golo Ahlenstiel
Reprogramming—Evolving Path to Functional Surrogate β-Cells
Cells
β-cell
diabetes mellitus
cell sources
reprogramming
insulin
title Reprogramming—Evolving Path to Functional Surrogate β-Cells
title_full Reprogramming—Evolving Path to Functional Surrogate β-Cells
title_fullStr Reprogramming—Evolving Path to Functional Surrogate β-Cells
title_full_unstemmed Reprogramming—Evolving Path to Functional Surrogate β-Cells
title_short Reprogramming—Evolving Path to Functional Surrogate β-Cells
title_sort reprogramming evolving path to functional surrogate β cells
topic β-cell
diabetes mellitus
cell sources
reprogramming
insulin
url https://www.mdpi.com/2073-4409/11/18/2813
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AT scottread reprogrammingevolvingpathtofunctionalsurrogatebcells
AT goloahlenstiel reprogrammingevolvingpathtofunctionalsurrogatebcells