Evidence map›Paper›PMID 24101377›Full record

ArticleThe Journal of experimental medicine2013

RhoA GTPase controls cytokinesis and programmed necrosis of hematopoietic progenitors.

Xuan Zhou, Maria Carolina Florian, Paritha Arumugam, Xiaoyi Chen, Jose A Cancelas, Richard Lang, Punam Malik, Hartmut Geiger, Yi Zheng

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
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  5. Article
  6. Article
  7. Article
  8. Review
  9. Linking cell cycle to hematopoietic stem cell fate decisions.Frontiers in cell and developmental biology · 2023
    Review
  10. Role of Rho GTPases in stem cell regulation.Biochemical Society transactions · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Rational targeting Cdc42 restrains Th2 cell differentiation and prevents allergic airway inflammation.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2019
    Article
  17. Article
  18. Article
  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

9 authors at 5 institutions in 3 countries.

Xuan ZhouDivision of Experimental Hematology and Cancer Biology, 2 Molecular and Development Biology Graduate Program, 3 Division of Ophthalmology, and 4 Division of Developmental Biology, Cincinnati Children's Research Foundation, University of Cincinnati, Cincinnati, OH 45229.
Maria Carolina Florian
Paritha Arumugam
Xiaoyi Chen
Jose A Cancelas
Richard Lang
Punam Malik
Hartmut Geiger
Yi Zheng
Cincinnati Children's Hospital Medical Center · USUniversity of Cincinnati · USInstitut thématique Génétique, génomique et bioinformatique · FROphthalmology Associates (United States) · USUniversität Ulm · DE

Funding

Cincinnati Center for Excellence in Molecular HematologyP30DK090971 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI ZHENG, YI · 2010 to 2015
$4.0M
Lineage Determination and Tissue HomeOstasis in the aged Hematopoietic SystemR01AG040118 · NIA · CINCINNATI CHILDRENS HOSP MED CTR · PI GEIGER, HARTMUT, ZHENG, YI · 2011 to 2015
$1.7M
Targeting Cdc42 in leukemia stem cellsR01CA150547 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI MULLOY, JAMES C, ZHENG, YI · 2010 to 2014
$1.5M
NCI NIH HHS R01 CA150547NCI NIH HHS R01CA150547NIA NIH HHS R01 AG040118NIA NIH HHS R01AG040118NIDDK NIH HHS P30 DK090971
6 · The paper itself

Abstract

Hematopoietic progenitor cells (HPCs) are central to hematopoiesis as they provide large numbers of lineage-defined blood cells necessary to sustain blood homeostasis. They are one of the most actively cycling somatic cells, and their precise control is critical for hematopoietic homeostasis. The small GTPase RhoA is an intracellular molecular switch that integrates cytokine, chemokine, and adhesion signals to coordinate multiple context-dependent cellular processes. By using a RhoA conditional knockout mouse model, we show that RhoA deficiency causes a multilineage hematopoietic failure that is associated with defective multipotent HPCs. Interestingly, RhoA(-/-) hematopoietic stem cells retained long-term engraftment potential but failed to produce multipotent HPCs and lineage-defined blood cells. This multilineage hematopoietic failure was rescued by reconstituting wild-type RhoA into the RhoA(-/-) Lin(-)Sca-1(+)c-Kit(+) compartment. Mechanistically, RhoA regulates actomyosin signaling, cytokinesis, and programmed necrosis of the HPCs, and loss of RhoA results in a cytokinesis failure of HPCs manifested by an accumulation of multinucleated cells caused by failed abscission of the cleavage furrow after telophase. Concomitantly, the HPCs show a drastically increased death associated with increased TNF-RIP-mediated necrosis. These results show that RhoA is a critical and specific regulator of multipotent HPCs during cytokinesis and thus essential for multilineage hematopoiesis.

Indexed as

CytokinesisActomyosinAnimalsApoptosisAutophagyCarrier ProteinsCell AdhesionCell LineageChemokine CXCL12ChemotaxisForminsHEK293 CellsHematopoiesisHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHomeostasisActomyosinCarrier ProteinsChemokine CXCL12Diap1 protein, mouseForminsrhoA GTP-Binding Proteinrho-Associated Kinases

Identifiers

PMID24101377
PMCPMC3804933
OpenAlexW2117800430

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.