Evidence map›Paper›PMID 30814559›Full record

ArticleScientific reports2019

Critical Functionality Effects from Storage Temperature on Human Induced Pluripotent Stem Cell-Derived Retinal Pigment Epithelium Cell Suspensions.

Shohei Kitahata, Yuji Tanaka, Kanji Hori, Cody Kime, Sunao Sugita, Hiroshi Ueda, Masayo Takahashi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  12. Pluripotent Stem Cells for Cell Therapy.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
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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

7 authors at 4 institutions in 1 country.

Shohei KitahataLaboratory for Retinal Regeneration, Biosystems Dynamics Research, RIKEN, Kobe, 650-0047, Japan.
Yuji TanakaLaboratory for Retinal Regeneration, Biosystems Dynamics Research, RIKEN, Kobe, 650-0047, Japan. yuji.tanaka@riken.jp.
Kanji HoriLaboratory for Retinal Regeneration, Biosystems Dynamics Research, RIKEN, Kobe, 650-0047, Japan.ORCID 0000-0002-3658-0954
Cody KimeLaboratory for Retinal Regeneration, Biosystems Dynamics Research, RIKEN, Kobe, 650-0047, Japan.
Sunao SugitaLaboratory for Retinal Regeneration, Biosystems Dynamics Research, RIKEN, Kobe, 650-0047, Japan.
Hiroshi UedaDepartment of Pharmacology and Therapeutic Innovation, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, 852-8521, Japan.
Masayo TakahashiLaboratory for Retinal Regeneration, Biosystems Dynamics Research, RIKEN, Kobe, 650-0047, Japan.
RIKEN Center for Biosystems Dynamics Research · JPJuntendo University · JPKyoto University · JPNagasaki University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human induced pluripotent stem cell (hiPSC)-derived retinal pigment epithelium (hiPSC-RPE) cells suspension have the potential for regenerative treatment. However, practical regenerative applications with hiPSC-RPE cells require the development of simple and cost-effective non-freezing preservation methods. We investigated the effect of non-freezing temperatures on suspended hiPSC-RPE cells in various conditions and analysed mechanisms of cell death, anoikis, Rho GTPases, hypoxia, microtubule destruction, and cell metabolism. Cells stored at 37 °C had the lowest viability due to hypoxia from high cell metabolism and cell deposits, and cells preserved at 4 °C were damaged via microtubule fragility. Cell suspensions at 16 °C were optimal with drastically reduced apoptosis and negligible necrosis. Moreover, surviving cells proliferated and secreted key proteins normally, compared to cells without preservation. hiPSC-RPE cell suspensions were optimally preserved at 16 °C. Temperatures above or below the optimal temperature decreased cell viability significantly yet differentially by mechanisms of cell death, cellular metabolism, microtubule destruction, and oxygen tension, all relevant to cell conditions. Surviving cells are expected to function as grafts where high cell death is often reported. This study provides new insight into various non-freezing temperature effects on hiPSC-RPE cells that are highly relevant to clinical applications and may improve cooperation between laboratories and hospitals.

Indexed as

Cell DeathCell DifferentiationCell HypoxiaTemperatureHumansInduced Pluripotent Stem CellsMicrotubulesRetinal Pigment Epitheliumrho GTP-Binding ProteinsSuspensionsrho GTP-Binding ProteinsSuspensions

Identifiers

PMID30814559
PMCPMC6393435
OpenAlexW2916881474

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.