Evidence map›Paper›PMID 31266807›Full record

ArticleThe Journal of biological chemistry2019

The mitophagy receptor Bcl-2-like protein 13 stimulates adipogenesis by regulating mitochondrial oxidative phosphorylation and apoptosis in mice.

Makoto Fujiwara, Li Tian, Phuong T Le, Victoria E DeMambro, Kathleen A Becker, Clifford J Rosen, Anyonya R Guntur

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
9.1field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
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  10. Molecular Characterization and Expression Changes of theCurrent issues in molecular biology · 2024
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  16. Mitophagy in metabolic syndrome.Journal of clinical hypertension (Greenwich, Conn.) · 2023
    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

7 authors at 2 institutions in 1 country.

Makoto FujiwaraCenter for Clinical and Translational Research, Maine Medical Center Research Institute, Scarborough, Maine 04074.
Li TianCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, Maine 04074.
Phuong T LeCenter for Clinical and Translational Research, Maine Medical Center Research Institute, Scarborough, Maine 04074.
Victoria E DeMambroCenter for Clinical and Translational Research, Maine Medical Center Research Institute, Scarborough, Maine 04074.
Kathleen A BeckerCenter for Clinical and Translational Research, Maine Medical Center Research Institute, Scarborough, Maine 04074.
Clifford J RosenCenter for Clinical and Translational Research, Maine Medical Center Research Institute, Scarborough, Maine 04074.
Anyonya R GunturCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, Maine 04074 guntua@mmc.org.ORCID 0000-0001-6366-200X
Maine Medical Center Research Institute · USMaine Medical Center · US

Funding

Understanding Factors Influencing COVID-19 Testing and Vaccination in Immigrant Low-income and Homeless Populations and Testing Targeted InterventionsU54GM115516 · NIGMS · MAINEHEALTH · PI Robert A Koza · 2017 to 2026
$51.6M
The role of night shift work in metabolic disorders during and after pregnancyP20GM121301 · NIGMS · MAINEHEALTH · PI Elizabeth Scharnetzki · 2017 to 2026
$25.1M
Interdisciplinary Study of Marrow Adiposity, Mineral Metabolism & Energy BalanceR24DK092759 · NIDDK · MAINEHEALTH · PI HOROWITZ, MARK C, MACDOUGALD, ORMOND A · 2011 to 2019
$13.0M
Progenitor Cell Analysis CoreP30GM106391 · NIGMS · MAINEHEALTH · PI WOJCHOWSKI, DON MICHAEL · 2013 to 2017
$5.7M
Role of MitoNEET in regulating osteoblast bioenergetics and catabolismR03AR068095 · NIAMS · MAINEHEALTH · PI GUNTUR, ANYONYA R · 2016 to 2018
$234k
NIAMS NIH HHS R03 AR068095NIDDK NIH HHS R24 DK092759NIGMS NIH HHS P20 GM121301NIGMS NIH HHS P30 GM106391NIGMS NIH HHS U54 GM115516
6 · The paper itself

Abstract

Metabolic programming of bone marrow stromal cells (BMSCs) could influence the function of progenitor osteoblasts or adipocytes and hence determine skeletal phenotypes. Adipocytes predominantly utilize oxidative phosphorylation, whereas osteoblasts use glycolysis to meet ATP demand. Here, we compared progenitor differentiation from the marrow of two inbred mouse strains, C3H/HeJ (C3H) and C57BL6J (B6). These strains differ in both skeletal mass and bone marrow adiposity. We hypothesized that genetic regulation of metabolic programs controls skeletal stem cell fate. Our experiments identified Bcl-2-like protein 13 (Bcl2l13), a mitochondrial mitophagy receptor, as being critical for adipogenic differentiation. We also found that Bcl2l13 is differentially expressed in the two mouse strains, with C3H adipocyte progenitor differentiation being accompanied by a >2-fold increase in Bcl2l13 levels relative to B6 marrow adipocytes. Bcl2l13 expression also increased during adipogenic differentiation in mouse ear mesenchymal stem cells (eMSCs) and the murine preadipocyte cell line 3T3-L1. The higher Bcl2l13 expression correlated with increased mitochondrial fusion and biogenesis. Importantly,

Indexed as

ApoptosisMitophagyOxidative PhosphorylationAdipogenesisAnimalsCells, CulturedMiceMice, Inbred C3HMice, Inbred C57BLMitochondriaProto-Oncogene Proteins c-bcl-2BCL2L13 protein, mouseProto-Oncogene Proteins c-bcl-2adipocyteadipogenesisapoptosisB-cell lymphoma 2 (Bcl-2) familyBcl-2-like protein 13 (Bcl2l13)bone marrowenergy metabolismlineage determinationmetabolic reprogrammingmitochondriamitochondrial metabolismmitophagyoxidative phosphorylation

Identifiers

PMID31266807
PMCPMC6709636
OpenAlexW2955145478

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.