Evidence map›Paper›PMID 37276417›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

ROS signaling-induced mitochondrial Sgk1 expression regulates epithelial cell renewal.

Yingxiang Li, Chengdong Liu, Luke Rolling, Veronica Sikora, Zhimin Chen, Jack Gurwin, Caroline Barabell, Jiandie Lin, Cunming Duan

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Cells · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Mitochondrial function and gastrointestinal diseases.Nature reviews. Gastroenterology & hepatology · 2024
    Review
  9. The role of serum/glucocorticoid-regulated kinase 1 in brain function following cerebral ischemia.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2024
    Article
  10. Review
  11. 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

9 authors at 1 institution in 1 country.

Yingxiang LiDepartment of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.ORCID 0000-0001-6671-2965
Chengdong LiuDepartment of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.
Luke RollingDepartment of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.ORCID 0009-0000-2398-9681
Veronica SikoraDepartment of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.ORCID 0000-0003-0463-5321
Zhimin ChenLife Science Institute, University of Michigan, Ann Arbor, MI 48109.ORCID 0000-0003-4241-7122
Jack GurwinDepartment of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.ORCID 0009-0007-5770-9124
Caroline BarabellDepartment of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.
Jiandie LinLife Science Institute, University of Michigan, Ann Arbor, MI 48109.ORCID 0000-0001-8069-5647
Cunming DuanDepartment of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.ORCID 0000-0001-6794-2762
University of Michigan · US

Funding

Research Training in BiogerontologyT32AG000114 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCOTT PLETCHER · 1985 to 2026
$12.4M
NIA NIH HHS T32 AG000114
6 · The paper itself

Abstract

Many types of differentiated cells can reenter the cell cycle upon injury or stress. The underlying mechanisms are still poorly understood. Here, we investigated how quiescent cells are reactivated using a zebrafish model, in which a population of differentiated epithelial cells are reactivated under a physiological context. A robust and sustained increase in mitochondrial membrane potential was observed in the reactivated cells. Genetic and pharmacological perturbations show that elevated mitochondrial metabolism and ATP synthesis are critical for cell reactivation. Further analyses showed that elevated mitochondrial metabolism increases mitochondrial ROS levels, which induces Sgk1 expression in the mitochondria. Genetic deletion and inhibition of Sgk1 in zebrafish abolished epithelial cell reactivation. Similarly, ROS-dependent mitochondrial expression of SGK1 promotes S phase entry in human breast cancer cells. Mechanistically, SGK1 coordinates mitochondrial activity with ATP synthesis by phosphorylating F

Indexed as

MitochondriaZebrafishAdenosine TriphosphateAnimalsEpithelial CellsHumansReactive Oxygen SpeciesAdenosine TriphosphateReactive Oxygen SpeciesF1Fo-ATP synthaseIGF/insulin signalingmitochondrial membrane potentialreactive oxygen speciesserum- and glucocorticoid-regulated kinase 1

Identifiers

PMID37276417
PMCPMC10268254
OpenAlexW4379468999

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.