Evidence map›Paper›PMID 27711254›Full record

ArticlePloS one2016

Reversible Cryopreservation of Living Cells Using an Electron Microscopy Cryo-Fixation Method.

Jan Huebinger, Hong-Mei Han, Markus Grabenbauer

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–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

10 citing papers in PubMed.

  1. Article
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  5. Review
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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.

Jan HuebingerDepartment of Systemic Cell Biology, Max-Planck-Institute of Molecular Physiology, Otto-Hahn-Str. 11, D-44227 Dortmund, Germany.
Hong-Mei HanDepartment of Systemic Cell Biology, Max-Planck-Institute of Molecular Physiology, Otto-Hahn-Str. 11, D-44227 Dortmund, Germany.
Markus GrabenbauerDepartment of Systemic Cell Biology, Max-Planck-Institute of Molecular Physiology, Otto-Hahn-Str. 11, D-44227 Dortmund, Germany.ORCID http://orcid.org/0000-0002-9156-5968

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rapid cooling of aqueous solutions is a useful approach for two important biological applications: (I) cryopreservation of cells and tissues for long-term storage, and (II) cryofixation for ultrastructural investigations by electron and cryo-electron microscopy. Usually, both approaches are very different in methodology. Here we show that a novel, fast and easy to use cryofixation technique called self-pressurized rapid freezing (SPRF) is-after some adaptations-also a useful and versatile technique for cryopreservation. Sealed metal tubes with high thermal diffusivity containing the samples are plunged into liquid cryogen. Internal pressure builds up reducing ice crystal formation and therefore supporting reversible cryopreservation through vitrification of cells. After rapid rewarming of pressurized samples, viability rates of > 90% can be reached, comparable to best-performing of the established rapid cooling devices tested. In addition, the small SPRF tubes allow for space-saving sample storage and the sealed containers prevent contamination from or into the cryogen during freezing, storage, or thawing.

Indexed as

AnimalsCaenorhabditis elegansCell SurvivalChlorocebus aethiopsCOS CellsCryoelectron MicroscopyCryopreservationCryoprotective AgentsFreezingHeLa CellsHumansPressureSaccharomyces cerevisiaeVitrificationCryoprotective Agents

Identifiers

PMID27711254
PMCPMC5053471

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.