Evidence map›Paper›PMID 30279440›Full record

ArticleScientific reports2018

Primary rat LSECs preserve their characteristic phenotype after cryopreservation.

Viola Mönkemöller, Hong Mao, Wolfgang Hübner, Gianina Dumitriu, Peter Heimann, Gahl Levy, Thomas Huser, Barbara Kaltschmidt, Christian Kaltschmidt, Cristina I Øie

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. 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

10 authors.

Viola MönkemöllerBiomolecular Photonics, Department of Physics, Bielefeld University, Universitätsstr. 25, 33615, Bielefeld, Germany.
Hong MaoFaculty of Health Sciences, Department of Medical Biology, Vascular Biology Research Group, UiT-The Arctic University of Norway, 9037, Tromsø, Norway.
Wolfgang HübnerBiomolecular Photonics, Department of Physics, Bielefeld University, Universitätsstr. 25, 33615, Bielefeld, Germany.
Gianina DumitriuFaculty of Health Sciences, Department of Medical Biology, Vascular Biology Research Group, UiT-The Arctic University of Norway, 9037, Tromsø, Norway.
Peter HeimannCell Biology and Molecular Neurobiology, Department of Biology, Bielefeld University, Universitätsstr. 25, 33615, Bielefeld, Germany.
Gahl LevyFaculty of Health Sciences, Department of Medical Biology, Vascular Biology Research Group, UiT-The Arctic University of Norway, 9037, Tromsø, Norway.
Thomas HuserBiomolecular Photonics, Department of Physics, Bielefeld University, Universitätsstr. 25, 33615, Bielefeld, Germany.ORCID http://orcid.org/0000-0003-2348-7416
Barbara KaltschmidtCell Biology and Molecular Neurobiology, Department of Biology, Bielefeld University, Universitätsstr. 25, 33615, Bielefeld, Germany.
Christian KaltschmidtCell Biology and Molecular Neurobiology, Department of Biology, Bielefeld University, Universitätsstr. 25, 33615, Bielefeld, Germany.
Cristina I ØieFaculty of Health Sciences, Department of Medical Biology, Vascular Biology Research Group, UiT-The Arctic University of Norway, 9037, Tromsø, Norway. cristina.ionica.oie@uit.no.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver disease is a leading cause of morbidity and mortality worldwide. Recently, the liver non-parenchymal cells have gained increasing attention for their potential role in the development of liver disease. Liver sinusoidal endothelial cells (LSECs), a specialized type of endothelial cells that have unique morphology and function, play a fundamental role in maintaining liver homeostasis. Current protocols for LSEC isolation and cultivation rely on freshly isolated cells which can only be maintained differentiated in culture for a few days. This creates a limitation in the use of LSECs for research and a need for a consistent and reliable source of these cells. To date, no LSEC cryopreservation protocols have been reported that enable LSECs to retain their functional and morphological characteristics upon thawing and culturing. Here, we report a protocol to cryopreserve rat LSECs that, upon thawing, maintain full LSEC-signature features: fenestrations, scavenger receptor expression and endocytic function on par with freshly isolated cells. We have confirmed these features by a combination of biochemical and functional techniques, and super-resolution microscopy. Our findings offer a means to standardize research using LSECs, opening the prospects for designing pharmacological strategies for various liver diseases, and considering LSECs as a therapeutic target.

Indexed as

Endothelial CellsAnimalsCells, CulturedCell SeparationCryopreservationLiverMalePrimary Cell CultureRatsRats, Sprague-Dawley

Identifiers

PMID30279440
PMCPMC6168544

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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.