Evidence map›Paper›PMID 35073969›Full record

ArticleStem cell research & therapy2022

Cell maturation influences the ability of hESC-RPE to tolerate cellular stress.

Taina Viheriälä, Heidi Hongisto, Juhana Sorvari, Heli Skottman, Soile Nymark, Tanja Ilmarinen

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.6field-weighted citation impact, top 9% of its field
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

7 citing papers in PubMed, 31 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Taina ViheriäläBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Heidi HongistoBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Juhana SorvariBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Heli Skottman *BioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Soile Nymark *BioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Tanja IlmarinenBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland. tanja.ilmarinen@tuni.fi.ORCID 0000-0002-4609-8897
Tampere University · FITampere University of Applied Sciences · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTransplantation of human pluripotent stem cell-derived retinal pigment epithelium (RPE) is an urgently needed treatment for the cure of degenerative diseases of the retina. The transplanted cells must tolerate cellular stress caused by various sources such as retinal inflammation and regain their functions rapidly after the transplantation. We have previously shown the maturation level of the cultured human embryonic stem cell-derived RPE (hESC-RPE) cells to influence for example their calcium (Ca

methodsHere, we analyzed the ability of the hESC-RPE populations with early (3 weeks) and late (12 weeks) maturation status to tolerate cellular stress caused by chemical cell stressors protease inhibitor (MG132) or hydrogen peroxide (H

resultsThe hESC-RPE population with late maturation status consistently showed improved tolerance to cellular stress in comparison to the population with early maturity. After the treatments, the early maturation status of hESC-RPE monolayer showed impaired barrier properties. The hESC-RPE with early maturity status also exhibited reduced phagocytic and Ca

conclusionsOur results suggest that due to better tolerance to cellular stress, the late maturation status of hESC-RPE population is superior compared to monolayers with early maturation status in the transplantation therapy settings.

Indexed as

Human Embryonic Stem CellsPluripotent Stem CellsCell DifferentiationHumansHydrogen PeroxideRetinal Pigment EpitheliumHydrogen PeroxideCell therapyHuman pluripotent stem cellsOxidative stressRetinal pigment epithelial cells

Identifiers

PMID35073969
PMCPMC8785579
OpenAlexW4207013536

What OpenQuestion holds

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Registered trials

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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 OpenQuestion graph.