Evidence map›Paper›PMID 31225513›Full record

ReviewCell stress2019

Remodeling of mitochondrial morphology and function: an emerging hallmark of cellular reprogramming.

Anuj Rastogi, Piyush Joshi, Ela Contreras, Vivian Gama

Abstract readReview
In one paragraph

Review in Cell stress, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

  1. Review
  2. Article
  3. Prenatal Alcohol Exposure and Mitochondrial Function in the Brain.Advances in experimental medicine and biology · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

4 authors.

Anuj RastogiDepartment of Cell & Developmental Biology, Vanderbilt University, Nashville, TN 37240.
Piyush JoshiNeuroscience Program, Vanderbilt University Medical Center, Nashville, TN 37240.
Ela ContrerasDepartment of Cell & Developmental Biology, Vanderbilt University, Nashville, TN 37240.
Vivian GamaDepartment of Cell & Developmental Biology, Vanderbilt University, Nashville, TN 37240.

Funding

TRAINING PROGRAM IN ENVIRONMENTAL TOXICOLOGYT32ES007028 · NIEHS · VANDERBILT UNIVERSITY · PI F PETER Guengerich, Fiona Edith Harrison · 1985 to 2026
$15.7M
The BCL-2 family controls stem cell identity by regulating mitochondrial dynamics and primingR35GM128915 · NIGMS · VANDERBILT UNIVERSITY · PI Vivian Gama · 2018 to 2026
$3.8M
Apoptotic Proteins as Molecular Modulators of Stem Cell FateR00CA178190 · NCI · VANDERBILT UNIVERSITY · PI GAMA, VIVIAN · 2015 to 2017
$747k
(PQ5) Assessing the contribution of mitochondrial heterogeneity to gliomagenesis using single cell approachesR21CA227483 · NCI · VANDERBILT UNIVERSITY · PI GAMA, VIVIAN · 2019 to 2020
$376k
NCI NIH HHS R00 CA178190NCI NIH HHS R21 CA227483NIEHS NIH HHS T32 ES007028NIGMS NIH HHS R35 GM128915
6 · The paper itself

Abstract

Research in the stem cell field has traditionally focused on understanding key transcriptional factors that provide pluripotent cell identity. However, much less is known about other critical non-transcriptional signaling networks that govern stem cell identity. Although we continue to gain critical insights into the mechanisms underlying mitochondrial morphology and function during cellular reprogramming - the process of reverting the fate of a differentiated cell into a stem cell, many uncertainties remain. Recent studies suggest an emerging landscape in which mitochondrial morphology and function have an active role in maintaining and regulating changes in cell identity. In this review, we will focus on these emerging concepts as crucial modulators of cellular reprogramming. Recognition of the widespread applicability of these concepts will increase our understanding of the mitochondrial mechanisms involved in cell identity, cell fate and disease.

Indexed as

apoptosisBCL-2 familymitochondriamitochondrial dynamics

Identifiers

PMID31225513
PMCPMC6558935

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.