Evidence map›Paper›PMID 24508650›Full record

ArticleCryobiology2014

Characterization and modulation of human mesenchymal stem cell stress pathway response following hypothermic storage.

William L Corwin, John M Baust, John G Baust, Robert G Van Buskirk

Abstract read
In one paragraph

Article in Cryobiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-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

9 citing papers in PubMed, 24 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

4 authors at 2 institutions in 1 country.

William L CorwinCPSI Biotech, 2 Court St, Owego, NY 13827, United States; Institute of Biomedical Technology, Binghamton University, Binghamton, NY 13902, United States. Electronic address: WCorwin@CPSIBiotech.com.
John M BaustCPSI Biotech, 2 Court St, Owego, NY 13827, United States; Institute of Biomedical Technology, Binghamton University, Binghamton, NY 13902, United States.
John G BaustInstitute of Biomedical Technology, Binghamton University, Binghamton, NY 13902, United States; Department of Biological Sciences, Binghamton University, Binghamton, NY 13902, United States.
Robert G Van BuskirkCPSI Biotech, 2 Court St, Owego, NY 13827, United States; Institute of Biomedical Technology, Binghamton University, Binghamton, NY 13902, United States; Department of Biological Sciences, Binghamton University, Binghamton, NY 13902, United States.
Binghamton University · USCell Preservation Services (United States) · US

Funding

Enhanced Bioprocessing Strategies for Human Mesenchymal Stem CellsR43RR032140 · NCRR · CELL PRESERVATION SERVICES, INC. · PI BAUST, JOHN M · 2011 to 2011
$369k
NCRR NIH HHS 1R43RR032140-01NCRR NIH HHS R43 RR032140
6 · The paper itself

Abstract

Human mesenchymal stem cell (hMSC) research has grown exponentially in the last decade. The ability to process and preserve these cells is vital to their use in stem cell therapy. As such, understanding the complex, molecular-based stress responses associated with biopreservation is necessary to improve outcomes and maintain the unique stem cell properties specific to hMSC. In this study hMSC were exposed to cold storage (4°C) for varying intervals in three different media. The addition of resveratrol or salubrinal was studied to determine if either could improve cell tolerance to cold. A rapid elevation in apoptosis at 1h post-storage as well as increased levels of necrosis through the 24h of recovery was noted in samples. The addition of resveratrol resulted in significant improvements to hMSC survival while the addition of salubrinal revealed a differential response based on the media utilized. Decreases in both apoptosis and necrosis together with decreased cell stress/death signaling protein levels were observed following modulation. Further, ER stress and subsequent unfolded protein response (UPR) stress pathway activation was implicated in response to hMSC hypothermic storage. This study is an important first step in understanding hMSC stress responses to cold exposure and demonstrates the impact of targeted molecular modulation of specific stress pathways on cold tolerance thereby yielding improved outcomes. Continued research is necessary to further elucidate the molecular mechanisms involved in hypothermic-induced hMSC cell death. This study has demonstrated the potential for improving hMSC processing and storage through targeting select cell stress pathways.

Indexed as

ApoptosisBlotting, WesternCell SurvivalCinnamatesCryopreservationCryoprotective AgentsFlow CytometryHumansMesenchymal Stem CellsNecrosisOsmoregulationResveratrolStilbenesStress, PhysiologicalThioureaCinnamatesCryoprotective AgentsResveratrolsalubrinalStilbenesThioureaApoptosisER stressHypothermic storageMesenchymal stem cellNecrosisResveratrolSalubrinalUnfolded protein response

Identifiers

PMID24508650
PMCPMC4001798
OpenAlexW2028014656

What OpenQuestion holds

Textmetadata
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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 OpenQuestion graph.