Evidence map›Paper›PMID 24709813›Full record

ArticlePloS one2014

Prohibitin 2 regulates the proliferation and lineage-specific differentiation of mouse embryonic stem cells in mitochondria.

Megumi Kowno, Kanako Watanabe-Susaki, Hisako Ishimine, Shinji Komazaki, Kei Enomoto, Yasuhiro Seki, Ying Ying Wang, Yohei Ishigaki, Naoto Ninomiya, Taka-aki K Noguchi and 10 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 56 citations in OpenAlex.

  1. Trial
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  8. New insights into mitophagy and stem cells.Stem cell research & therapy · 2021
    Review
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  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Multifaceted role of prohibitin in cell survival and apoptosis.Apoptosis : an international journal on programmed cell death · 2015
    Review
  20. Metabolic restructuring and cell fate conversion.Cellular and molecular life sciences : CMLS · 2015
    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

20 authors at 5 institutions in 1 country.

Megumi KownoGraduate School of Life and Environmental Sciences, The University of Tsukuba, Tsukuba, Ibaraki, Japan.
Kanako Watanabe-SusakiResearch Center for Stem Cell Engineering, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki, Japan.
Hisako IshimineGraduate School of Life and Environmental Sciences, The University of Tsukuba, Tsukuba, Ibaraki, Japan; Research Center for Stem Cell Engineering, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki, Japan.
Shinji KomazakiDepartment of Anatomy, Saitama Medical School, Moroyama, Iruma, Saitama, Japan.
Kei EnomotoDepartment of Biological Science, Graduate School of Science, The University of Tokyo, Meguro, Tokyo, Japan.
Yasuhiro SekiDepartment of Life Sciences (Biology), Graduate School of Arts and Sciences, The University of Tokyo, Meguro, Tokyo, Japan.
Ying Ying WangResearch Center for Stem Cell Engineering, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki, Japan; Japan Society for the Promotion of Science (JSPS), Tsukuba, Ibaraki, Japan.
Yohei IshigakiGraduate School of Life and Environmental Sciences, The University of Tsukuba, Tsukuba, Ibaraki, Japan.
Naoto NinomiyaDepartment of Biological Science, Graduate School of Science, The University of Tokyo, Meguro, Tokyo, Japan.
Taka-aki K NoguchiGraduate School of Life and Environmental Sciences, The University of Tsukuba, Tsukuba, Ibaraki, Japan.
Yuko KokubuGraduate School of Life and Environmental Sciences, The University of Tsukuba, Tsukuba, Ibaraki, Japan.
Keigoh OhnishiGraduate School of Life and Environmental Sciences, The University of Tsukuba, Tsukuba, Ibaraki, Japan.
Yoshiro NakajimaResearch Center for Stem Cell Engineering, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki, Japan.
Kaoru KatoHealth Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki, Japan.
Atsushi IntohDepartment of Life Sciences (Biology), Graduate School of Arts and Sciences, The University of Tokyo, Meguro, Tokyo, Japan.
Hitomi TakadaResearch Center for Stem Cell Engineering, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki, Japan.
Norio YamakawaResearch Center for Stem Cell Engineering, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki, Japan.
Pi-Chao WangGraduate School of Life and Environmental Sciences, The University of Tsukuba, Tsukuba, Ibaraki, Japan.
Makoto AsashimaResearch Center for Stem Cell Engineering, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki, Japan; Department of Life Sciences (Biology), Graduate School of Arts and Sciences, The University of Tokyo, Meguro, Tokyo, Japan; Life Science Center of Tsukuba Advanced Research Alliance, The University of Tsukuba, Tsukuba, Ibaraki, Japan.
Akira KurisakiGraduate School of Life and Environmental Sciences, The University of Tsukuba, Tsukuba, Ibaraki, Japan; Research Center for Stem Cell Engineering, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki, Japan.
University of Tsukuba · JPNational Institute of Advanced Industrial Science and Technology · JPThe University of Tokyo · JPJapan Society for the Promotion of Science · JPSaitama Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe pluripotent state of embryonic stem (ES) cells is controlled by a network of specific transcription factors. Recent studies also suggested the significant contribution of mitochondria on the regulation of pluripotent stem cells. However, the molecules involved in these regulations are still unknown. METHODOLOGY/PRINCIPAL

findingsIn this study, we found that prohibitin 2 (PHB2), a pleiotrophic factor mainly localized in mitochondria, is a crucial regulatory factor for the homeostasis and differentiation of ES cells. PHB2 was highly expressed in undifferentiated mouse ES cells, and the expression was decreased during the differentiation of ES cells. Knockdown of PHB2 induced significant apoptosis in pluripotent ES cells, whereas enhanced expression of PHB2 contributed to the proliferation of ES cells. However, enhanced expression of PHB2 strongly inhibited ES cell differentiation into neuronal and endodermal cells. Interestingly, only PHB2 with intact mitochondrial targeting signal showed these specific effects on ES cells. Moreover, overexpression of PHB2 enhanced the processing of a dynamin-like GTPase (OPA1) that regulates mitochondrial fusion and cristae remodeling, which could induce partial dysfunction of mitochondria. CONCLUSIONS/SIGNIFICANCE: Our results suggest that PHB2 is a crucial mitochondrial regulator for homeostasis and lineage-specific differentiation of ES cells.

Indexed as

AnimalsCell DifferentiationCell LineCell LineageCell ProliferationEmbryonic Stem CellsGene Expression RegulationMediator ComplexMiceMitochondriaMitochondrial ProteinsProhibitinsRepressor ProteinsMed12 protein, mouseMediator ComplexMitochondrial ProteinsPhb2 protein, mouseProhibitinsRepressor Proteins

Identifiers

PMID24709813
PMCPMC3977857
OpenAlexW2000947415

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.