Evidence map›Paper›PMID 26741196›Full record

ArticleEndocrinology2016

Translocator Protein (TSPO) Affects Mitochondrial Fatty Acid Oxidation in Steroidogenic Cells.

Lan N Tu, Amy H Zhao, Mahmoud Hussein, Douglas M Stocco, Vimal Selvaraj

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

56 citing papers in PubMed, 93 citations in OpenAlex.

  1. Tanycytes: bloodhounds of the metabolic brain.Trends in endocrinology and metabolism: TEM · 2026
    Review
  2. Article
  3. STAR/STARD1: A mitochondrial intermembrane space cholesterol shuttle degraded through mitophagy.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. The Physiological and Pathological Role of Acyl-CoA Oxidation.International journal of molecular sciences · 2023
    Review
  11. Article
  12. Apoptotic proteins with non-apoptotic activity: expression and function in cancer.Apoptosis : an international journal on programmed cell death · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Allopregnanolone: Metabolism, Mechanisms of Action, and Its Role in Cancer.International journal of molecular sciences · 2022
    Review
  19. Article
  20. Article
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

5 authors at 3 institutions in 1 country.

Lan N TuDepartment of Animal Science (L.N.T., A.H.Z., M.H., V.S.), College of Agriculture and Life Sciences, Cornell University, Ithaca, New York 14853; and Department of Cell Biology and Biochemistry (D.M.S.), School of Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas 79430.
Amy H ZhaoDepartment of Animal Science (L.N.T., A.H.Z., M.H., V.S.), College of Agriculture and Life Sciences, Cornell University, Ithaca, New York 14853; and Department of Cell Biology and Biochemistry (D.M.S.), School of Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas 79430.
Mahmoud HusseinDepartment of Animal Science (L.N.T., A.H.Z., M.H., V.S.), College of Agriculture and Life Sciences, Cornell University, Ithaca, New York 14853; and Department of Cell Biology and Biochemistry (D.M.S.), School of Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas 79430.
Douglas M StoccoDepartment of Animal Science (L.N.T., A.H.Z., M.H., V.S.), College of Agriculture and Life Sciences, Cornell University, Ithaca, New York 14853; and Department of Cell Biology and Biochemistry (D.M.S.), School of Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas 79430.
Vimal SelvarajDepartment of Animal Science (L.N.T., A.H.Z., M.H., V.S.), College of Agriculture and Life Sciences, Cornell University, Ithaca, New York 14853; and Department of Cell Biology and Biochemistry (D.M.S.), School of Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas 79430.
Cornell University · USNew York State College of Agriculture & Life Sciences · USTexas Tech University · US

Funding

MITOCHONDRIAL PROTEINS AND LEYDIG CELL STEROIDOGENESISR37HD017481 · NICHD · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI STOCCO, DOUGLAS M · 1996 to 2005
$1.9M
MITOCHONDRIAL PROTEINS AND LEYDIG CELL STEROIDOGENESISR01HD017481 · NICHD · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI STOCCO, DOUGLAS M · 1985 to 2011
$1.5M
NICHD NIH HHS HD-017481NICHD NIH HHS R01 HD017481NICHD NIH HHS R37 HD017481
6 · The paper itself

Abstract

Translocator protein (TSPO), also known as the peripheral benzodiazepine receptor, is a highly conserved outer mitochondrial membrane protein present in specific subpopulations of cells within different tissues. In recent studies, the presumptive model depicting mammalian TSPO as a critical cholesterol transporter for steroidogenesis has been refuted by studies examining effects of Tspo gene deletion in vivo and in vitro, biochemical testing of TSPO cholesterol transport function, and specificity of TSPO-mediated pharmacological responses. Nevertheless, high TSPO expression in steroid-producing cells seemed to indicate an alternate function for this protein in steroidogenic mitochondria. To seek an explanation, we used CRISPR/Cas9-mediated TSPO knockout steroidogenic MA-10 Leydig cell (MA-10:TspoΔ/Δ) clones to examine changes to core mitochondrial functions resulting from TSPO deficiency. We observed that 1) MA-10:TspoΔ/Δ cells had a shift in substrate utilization for energy production from glucose to fatty acids with significantly higher mitochondrial fatty acid oxidation (FAO), and increased reactive oxygen species production; and 2) oxygen consumption rate, mitochondrial membrane potential, and proton leak were not different between MA-10:TspoΔ/Δ and MA-10:Tspo+/+ control cells. Consistent with this finding, TSPO-deficient adrenal glands from global TSPO knockout (Tspo(-/-)) mice also showed up-regulation of genes involved in FAO compared with the TSPO floxed (Tspo(fl/fl)) controls. These results demonstrate the first experimental evidence that TSPO can affect mitochondrial energy homeostasis through modulation of FAO, a function that appears to be consistent with high levels of TSPO expression observed in cell types active in lipid storage/metabolism.

Indexed as

AnimalsCell Line, TumorFatty AcidsGene Expression RegulationIon ChannelsIsocitrate DehydrogenaseLeydig CellsLipid MetabolismMaleMembrane Potential, MitochondrialMiceMice, KnockoutMitochondriaMitochondrial ProteinsOxidation-ReductionProgesteroneBzrp protein, mouseFatty AcidsIon ChannelsIsocitrate Dehydrogenaseisocitrate dehydrogenase 2, mouseMitochondrial ProteinsProgesteroneReactive Oxygen SpeciesReceptors, GABARNA, MessengerUncoupling Protein 2Vdac1 protein, mouseVoltage-Dependent Anion Channel 1

Identifiers

PMID26741196
PMCPMC4769361
OpenAlexW2232338922

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.