Evidence map›Paper›PMID 39273600›Full record

ArticleInternational journal of molecular sciences2024

From iPSCs to Pancreatic β Cells: Unveiling Molecular Pathways and Enhancements with Vitamin C and Retinoic Acid in Diabetes Research.

Felipe Arroyave, Yomaira Uscátegui, Fernando Lizcano

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Felipe ArroyaveCenter of Biomedical Investigation (CIBUS), Universidad de La Sabana, Chia 250008, Colombia.ORCID 0000-0003-4901-9469
Yomaira UscáteguiCenter of Biomedical Investigation (CIBUS), Universidad de La Sabana, Chia 250008, Colombia.
Fernando LizcanoCenter of Biomedical Investigation (CIBUS), Universidad de La Sabana, Chia 250008, Colombia.ORCID 0000-0002-2414-6894

Funding

Direccion General de Investigacion (DIN) from Universidad de La Sabana MED 255-2019 and MED 292-2020
6 · The paper itself

Abstract

Diabetes mellitus, a chronic and non-transmissible disease, triggers a wide range of micro- and macrovascular complications. The differentiation of pancreatic β-like cells (PβLCs) from induced pluripotent stem cells (iPSCs) offers a promising avenue for regenerative medicine aimed at treating diabetes. Current differentiation protocols strive to emulate pancreatic embryonic development by utilizing cytokines and small molecules at specific doses to activate and inhibit distinct molecular signaling pathways, directing the differentiation of iPSCs into pancreatic β cells. Despite significant progress and improved protocols, the full spectrum of molecular signaling pathways governing pancreatic development and the physiological characteristics of the differentiated cells are not yet fully understood. Here, we report a specific combination of cofactors and small molecules that successfully differentiate iPSCs into PβLCs. Our protocol has shown to be effective, with the resulting cells exhibiting key functional properties of pancreatic β cells, including the expression of crucial molecular markers (pdx1, nkx6.1, ngn3) and the capability to secrete insulin in response to glucose. Furthermore, the addition of vitamin C and retinoic acid in the final stages of differentiation led to the overexpression of specific β cell genes.

Indexed as

Ascorbic AcidCell DifferentiationDiabetes MellitusInduced Pluripotent Stem CellsInsulin-Secreting CellsTretinoinBasic Helix-Loop-Helix ProteinsHomeodomain ProteinsHumansInsulinNerve Tissue ProteinsSignal TransductionTrans-ActivatorsAscorbic AcidBasic Helix-Loop-Helix ProteinsHomeodomain ProteinsInsulinNerve Tissue ProteinsNEUROG3 protein, humanNKX6-1 protein, humanpancreatic and duodenal homeobox 1 proteinTrans-ActivatorsTretinoincell therapydiabetesdifferentiationinsuliniPSCislet beta cells

Identifiers

PMID39273600
PMCPMC11395045

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.