Evidence map›Paper›PMID 32433698›Full record

ArticlePloS one2020

Stem cell function is conserved during short-term storage of cultured epidermal cell sheets at 12°C.

Håkon Ringstad, Sjur Reppe, Tine Hiorth Schøyen, Kim Alexander Tønseth, Tor Paaske Utheim, Catherine Joan Jackson

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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

  1. Pooled it
  2. Review
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.

Håkon RingstadDepartment of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.ORCID 0000-0002-7857-6881
Sjur ReppeDepartment of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.
Tine Hiorth SchøyenDepartment of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.ORCID 0000-0001-8281-5913
Kim Alexander TønsethFaculty of Medicine, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Tor Paaske UtheimDepartment of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.
Catherine Joan JacksonDepartment of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.ORCID 0000-0001-9683-2343

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transplantation of cultured epidermal cell sheets (CES) can be life-saving for patients with large area burns. CES have also been successfully used to regenerate eye and urethral epithelia in animal models. Short-term storage aims to extend the transplantation window, offers flexibility in timing surgery and allows testing of CES quality, phenotype and sterility. This study investigated extended CES storage and explored the effect of additional re-incubation recovery time following storage. The proliferative quality of stored confluent versus pre-confluent CES was also investigated using functional testing. CES were stored at 12°C and results compared to non-stored control CES. Investigation of timepoints during 15 days storage revealed that viability began to deteriorate by day 11 and was associated with increased lactate in the storage medium. The percentage of apoptotic cells also significantly increased by day 11. Flow cytometry analysis of integrin β1 expression and cell size indicated best retention of stem cells at 7 days of storage. Functional testing of pre-confluent and confluent cells following 7 days storage showed that pre-confluent cells responded well to 1-day re-incubation after storage; they became highly prolific, increasing in number by ~67%. Conversely, proliferation in stored confluent cells declined by ~50% with 1-day re-incubation. Pre-confluent stored CES also had far superior stem cell colony forming efficiency (CFE) performance compared to the confluent group. Re-incubation improved CFE in both groups, but the pre-confluent group again out-performed the confluent group with significantly more colonies. In conclusion, a maximum storage period of 7 days is recommended. Use of pre-confluent cells and one day recovery incubation greatly improves viability, colony-forming ability and proliferation of cells stored for 7 days at 12°C. Thus, these recommendations should be considered under culture and storage of high-quality CES for clinical use.

Indexed as

CryopreservationEpidermisCell CycleCell ProliferationCells, CulturedCell SurvivalCold TemperatureFemaleHumansStem CellsTime FactorsYoung Adult

Identifiers

PMID32433698
PMCPMC7239464

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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.