Evidence map›Paper›PMID 32350080›Full record

ArticleJournal of lipid research2020

Metabolic regulation of the lysosomal cofactor bis(monoacylglycero)phosphate in mice.

Gernot F Grabner, Nermeen Fawzy, Renate Schreiber, Lisa M Pusch, Dominik Bulfon, Harald Koefeler, Thomas O Eichmann, Achim Lass, Martina Schweiger, Gunther Marsche and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. 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

13 authors at 2 institutions in 1 country.

Gernot F GrabnerInstitute of Molecular Biosciences, University of Graz, Graz, Austria.
Nermeen FawzyInstitute of Molecular Biosciences, University of Graz, Graz, Austria.
Renate SchreiberInstitute of Molecular Biosciences, University of Graz, Graz, Austria.
Lisa M PuschInstitute of Molecular Biosciences, University of Graz, Graz, Austria.
Dominik BulfonInstitute of Molecular Biosciences, University of Graz, Graz, Austria.
Harald KoefelerOtto Loewi Research Center, and Center for Medical Research, Medical University of Graz, Graz, Austria; BioTechMed-Graz, Graz, Austria.
Thomas O EichmannInstitute of Molecular Biosciences, University of Graz, Graz, Austria; Center for Explorative Lipidomics, BioTechMed-Graz, Graz, Austria.
Achim LassInstitute of Molecular Biosciences, University of Graz, Graz, Austria; BioTechMed-Graz, Graz, Austria.
Martina SchweigerInstitute of Molecular Biosciences, University of Graz, Graz, Austria.
Gunther MarscheDivision of Pharmacology, Medical University of Graz, Graz, Austria; BioTechMed-Graz, Graz, Austria.
Gabriele SchoiswohlInstitute of Molecular Biosciences, University of Graz, Graz, Austria.
Ulrike TaschlerInstitute of Molecular Biosciences, University of Graz, Graz, Austria.
Robert ZimmermannInstitute of Molecular Biosciences, University of Graz, Graz, Austria; BioTechMed-Graz, Graz, Austria. Electronic address: mailto:robert.zimmermann@uni-graz.at.
University of Graz · ATMedical University of Graz · AT

Funding

Austrian Science Fund FWF DOC 50Austrian Science Fund FWF P 28882
6 · The paper itself

Abstract

Bis(monoacylglycero)phosphate (BMP), also known as lysobisphosphatidic acid, is a phospholipid that promotes lipid sorting in late endosomes/lysosomes by activating lipid hydrolases and lipid transfer proteins. Changes in the cellular BMP content therefore reflect an altered metabolic activity of the endolysosomal system. Surprisingly, little is known about the physiological regulation of BMP. In this study, we investigated the effects of nutritional and metabolic factors on BMP profiles of whole tissues and parenchymal and nonparenchymal cells. Tissue samples were obtained from fed, fasted, 2 h refed, and insulin-treated mice, as well as from mice housed at 5°C, 22°C, or 30°C. These tissues exhibited distinct BMP profiles that were regulated by the nutritional state in a tissue-specific manner. Insulin treatment was not sufficient to mimic refeeding-induced changes in tissue BMP levels, indicating that BMP metabolism is regulated by other hormonal or nutritional factors. Tissue fractionation experiments revealed that fasting drastically elevates BMP levels in hepatocytes and pancreatic cells. Furthermore, we observed that the BMP content in brown adipose tissue strongly depends on housing temperatures. In conclusion, our observations suggest that BMP concentrations adapt to the metabolic state in a tissue- and cell-type-specific manner in mice. Drastic changes observed in hepatocytes, pancreatic cells, and brown adipocytes suggest that BMP plays a role in the functional adaption to nutrient starvation and ambient temperature.

Indexed as

AnimalsEndosomesLysophospholipidsLysosomesMacrophagesMiceMonoglyceridesbis(monoacylglyceryl)phosphateLysophospholipidsMonoglyceridesadipose tissuebody temperatureinsulinlipid metabolismliverlysosomenutritional statepancreasphospholipids

Identifiers

PMID32350080
PMCPMC7328040
OpenAlexW3022835444

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.