Evidence map›Paper›PMID 21726514›Full record

ArticleExperimental hematology2011

Kinase suppressor of Ras (KSR1) modulates multiple kit-ligand-dependent mast cell functions.

Mia Chen, Sarah Burgin, Karl Staser, Yongzheng He, Xiaohong Li, Mikella Robinson, Li Jiang, Rebecca J Chan, David Ingram, D Wade Clapp

Open access · greenAbstract read
In one paragraph

Article in Experimental hematology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 49% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. Nerve Growth Factor and Autoimmune Diseases.Current issues in molecular biology · 2023
    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

10 authors at 2 institutions in 1 country.

Mia ChenDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, USA.
Sarah Burgin
Karl Staser
Yongzheng He
Xiaohong Li
Mikella Robinson
Li Jiang
Rebecca J Chan
David Ingram
D Wade Clapp
Indiana University – Purdue University Indianapolis · USIndiana University School of Medicine

Funding

Transgenic CoreP50NS052606 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI PARADA, LUIS FERNANDO · 2005 to 2014
$12.6M
Neurofibromatosis Type 1 Gene Regulates MyelopoiesisR01CA074177 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI CLAPP, DAVID W · 2002 to 2012
$3.6M
Fanconi Anemia stem cells allow molecular characterization of acute leukemiaR01CA138237 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI BAGBY, GROVER CARLTON, CLAPP, DAVID W · 2008 to 2012
$1.9M
Cancer Biology Training ProgramT32CA111198 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI ROMAN, ANN · 2005 to 2009
$1.8M
NCI NIH HHS R01 CA074177NCI NIH HHS R01 CA138237NCI NIH HHS R01 CA74177-06NCI NIH HHS T32 CA111198NINDS NIH HHS P50 NS052606
6 · The paper itself

Abstract

The intricately regulated Ras pathway coordinates multiple kit-ligand-induced mast cell functions, including chemotaxis, proliferation, and degranulation. However, the intracellular proteins that modulate the intensity and duration of stem cell factor-induced signals and the consequent cellular response are incompletely understood. Scaffolding proteins coordinate the spatial organization of mitogen-activated protein kinase proteins that may potentiate and/or inhibit cell functions. The kinase suppressor of Ras (KSR1) protein is known to function as a molecular scaffold and coordinates the organization of Raf/Mek/Erk in response to receptor tyrosine kinases. However, the impact of KSR1 in myeloid mast cell functions and in response to stem cell factor remains unknown. In the present study, we investigated the role of KSR1 in regulating cellular functions of bone marrow-derived mast cells of KSR1-deficient ((-/-)) mice. Genetic disruption of KSR1 resulted in both striking reductions in kit-ligand-mediated proliferation and degranulation, which are commonly attributed to mitogen-activated protein kinase signals. Surprisingly, disruption of the KSR1 scaffold also resulted in a decline in migration that is generally not linked to Raf-Erk signals. We found that loss of KSR1 does impact the biochemical activation of p21-activated kinase, a kinase that is known to modulate Raf-Erk signals and also F-actin polymerization key to mast cell migration. Collectively, these studies demonstrate that the scaffolding protein KSR1 has an important role in multiple kit-ligand-mediated mast cell functions. This study elucidates varied mast cell physiological functions for KSR1, including those related to cytoskeletal organization, and it suggests a novel molecular target for attenuating mast cell-mediated inflammation.

Indexed as

AnimalsBone Marrow CellsCell CycleCell DegranulationCell DivisionCells, CulturedCytoskeletonEnzyme ActivationExtracellular Signal-Regulated MAP KinasesInflammationMAP Kinase Signaling SystemMast CellsMiceMice, Knockoutp21-Activated KinasesProtein KinasesExtracellular Signal-Regulated MAP KinasesKSR-1 protein kinasep21-Activated KinasesProtein Kinasesraf KinasesStem Cell Factor

Identifiers

PMID21726514
PMCPMC3182112
OpenAlexW2027225523

What OpenQuestion holds

Textmetadata
LicenceTDM
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.