Evidence map›Paper›PMID 28277987›Full record

ArticleIslets2017

EndoC-βH1 cells display increased sensitivity to sodium palmitate when cultured in DMEM/F12 medium.

Camilla Krizhanovskii, Hjalti Kristinsson, Andris Elksnis, Xuan Wang, Hamid Gavali, Peter Bergsten, Raphael Scharfmann, Nils Welsh

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Islets, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

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  16. BRICHOS domain of Bri2 inhibits islet amyloid polypeptide (IAPP) fibril formation and toxicity in human beta cells.Proceedings of the National Academy of Sciences of the United States of America · 2018
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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

8 authors at 2 institutions in 2 countries.

Camilla Krizhanovskiia Science for Life Laboratory, Department of Medical Cell Biology , Uppsala University , Uppsala , Sweden.
Hjalti Kristinssona Science for Life Laboratory, Department of Medical Cell Biology , Uppsala University , Uppsala , Sweden.
Andris Elksnisa Science for Life Laboratory, Department of Medical Cell Biology , Uppsala University , Uppsala , Sweden.ORCID 0000-0003-0353-326X
Xuan Wanga Science for Life Laboratory, Department of Medical Cell Biology , Uppsala University , Uppsala , Sweden.
Hamid Gavalia Science for Life Laboratory, Department of Medical Cell Biology , Uppsala University , Uppsala , Sweden.
Peter Bergstena Science for Life Laboratory, Department of Medical Cell Biology , Uppsala University , Uppsala , Sweden.
Raphael Scharfmannb INSERM, U1016, Institut Cochin, Faculté de Médecine , Université Paris Descartes, Sorbonne Paris Cité , Paris , France.
Nils Welsha Science for Life Laboratory, Department of Medical Cell Biology , Uppsala University , Uppsala , Sweden.
Uppsala University · SEDélégation Paris 5 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aims - Human pancreatic islets are known to die in response to the free fatty acid of sodium palmitate when cultured in vitro. This is in contrast to EndoC-βH1 cells, which in our hands are not sensitive to the cell death-inducing effects sodium palmitate, making these cells seemingly unsuitable for lipotoxicity studies. However, the EndoC-βH1 cells are routinely cultured in a nutrient mixture based on Dulbecco's Modified Eagle Medium (DMEM), which may not be the optimal choice for studies dealing with lipotoxicity. The aim of the present investigation was to define culture conditions that render EndoC-βH1 cells sensitive to toxic effects of sodium palmitate. Methods - EndoC-βH1 cells were cultured at standard conditions in either DMEM or DMEM/F12 culture medium. Cell death was analyzed using propidium iodide staining and flow cytometry. Insulin release and content was quantified using a human insulin ELISA. Results - We presently observe that substitution of DMEM for a DMEM/Ham's F12 mixture (50%/50% vol/vol) renders the cells sensitive to the apoptotic effects of sodium palmitate and sodium palmitate + high glucose leading to an increased cell death. Supplementation of the DMEM culture medium with linoleic acid partially mimicked the effect of DMEM/F12. Culture of EndoC-βH1 cells in DMEM/F12 resulted also in increased proliferation, ROS production and insulin contents, but markers for metabolic stress, autophagy or amyloid deposits were unaffected. Conclusions - The culture conditions for EndoC-βH1 cells can be modified so these cells display signs of lipotoxicity in response to sodium palmitate.

Indexed as

ApoptosisCell ProliferationCulture MediaEnzyme InhibitorsGlucoseHumansInsulinInsulin-Secreting CellsLinoleic AcidPalmitic AcidReactive Oxygen SpeciesCulture MediaEnzyme InhibitorsGlucoseInsulinLinoleic AcidPalmitic AcidReactive Oxygen Speciescell deathEndoC-βH1 cellsinsulinROS productionsodium palmitate

Identifiers

PMID28277987
PMCPMC5465947
OpenAlexW2603933061

What OpenQuestion holds

Textmetadata
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.