Evidence map›Paper›PMID 31167138›Full record

ArticleCell reports2019

STRIPAK Members Orchestrate Hippo and Insulin Receptor Signaling to Promote Neural Stem Cell Reactivation.

Jon Gil-Ranedo, Eleanor Gonzaga, Karolina J Jaworek, Christian Berger, Torsten Bossing, Claudia S Barros

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.3field-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

33 citing papers in PubMed, 57 citations in OpenAlex.

  1. The Hox Gene,Molecular biology of the cell · 2025
    Article
  2. The Hox Gene,bioRxiv : the preprint server for biology · 2025
    Article
  3. Article
  4. Review
  5. Gene model for the ortholog ofmicroPublication biology · 2025
    Article
  6. STRIPAK, a fundamental signaling hub of eukaryotic development.Microbiology and molecular biology reviews : MMBR · 2024
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. The Hippo signaling pathway in gastric cancer.Acta biochimica et biophysica Sinica · 2023
    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

6 authors at 2 institutions in 2 countries.

Jon Gil-RanedoFaculty of Medicine and Dentistry, University of Plymouth, PL6 8BU Plymouth, UK.
Eleanor GonzagaFaculty of Medicine and Dentistry, University of Plymouth, PL6 8BU Plymouth, UK.
Karolina J JaworekFaculty of Medicine and Dentistry, University of Plymouth, PL6 8BU Plymouth, UK.
Christian BergerInstitute of Genetics, Johannes Gutenberg University, 55099 Mainz, Germany.
Torsten BossingFaculty of Medicine and Dentistry, University of Plymouth, PL6 8BU Plymouth, UK.
Claudia S BarrosFaculty of Medicine and Dentistry, University of Plymouth, PL6 8BU Plymouth, UK. Electronic address: claudia.barros@plymouth.ac.uk.
University of Plymouth · GBJohannes Gutenberg University Mainz · DE

Funding

Biotechnology and Biological Sciences Research Council BB/M004392/1
6 · The paper itself

Abstract

Adult stem cells reactivate from quiescence to maintain tissue homeostasis and in response to injury. How the underlying regulatory signals are integrated is largely unknown. Drosophila neural stem cells (NSCs) also leave quiescence to generate adult neurons and glia, a process that is dependent on Hippo signaling inhibition and activation of the insulin-like receptor (InR)/PI3K/Akt cascade. We performed a transcriptome analysis of individual quiescent and reactivating NSCs harvested directly from Drosophila brains and identified the conserved STRIPAK complex members mob4, cka, and PP2A (microtubule star, mts). We show that PP2A/Mts phosphatase, with its regulatory subunit Widerborst, maintains NSC quiescence, preventing premature activation of InR/PI3K/Akt signaling. Conversely, an increase in Mob4 and Cka levels promotes NSC reactivation. Mob4 and Cka are essential to recruit PP2A/Mts into a complex with Hippo kinase, resulting in Hippo pathway inhibition. We propose that Mob4/Cka/Mts functions as an intrinsic molecular switch coordinating Hippo and InR/PI3K/Akt pathways and enabling NSC reactivation.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAnimals, Genetically ModifiedBrainCell ProliferationCells, CulturedDrosophila melanogasterDrosophila ProteinsGene Expression ProfilingHippo KinasesIntracellular Signaling Peptides and ProteinsMitosisNerve Tissue ProteinsNeural Stem CellsPhosphatidylinositol 3-KinasesProtein Phosphatase 2Adaptor Proteins, Signal TransducingCka protein, DrosophilaDrosophila ProteinsHippo Kinaseshpo protein, DrosophilaIntracellular Signaling Peptides and ProteinsMob4 protein, Drosophilamts protein, DrosophilaNerve Tissue ProteinsPhosphatidylinositol 3-KinasesProtein Phosphatase 2Protein Serine-Threonine KinasesProto-Oncogene Proteins c-aktReceptor, InsulinHippo signalingInR/PI3K/Akt signalingneural stem cellsquiescencereactivationSTRIPAK members

Identifiers

PMID31167138
PMCPMC6581792
OpenAlexW2948027075

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.