Evidence map›Paper›PMID 22262848›Full record

ArticleThe Journal of biological chemistry2012

The role of Ras guanine nucleotide releasing protein 4 in Fc epsilonRI-mediated signaling, mast cell function, and T cell development.

Minghua Zhu, Deirdre M Fuller, Weiguo Zhang

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

20 citing papers in PubMed, 25 citations in OpenAlex.

  1. RasGRP4 Exacerbates Diabetic Kidney Fibrosis via Aloxe3-Mediated Oxidative Stress and Scar-Associated Macrophage Activation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  2. Acta biochimica et biophysica Sinica · 2024
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  20. Regulation of Ras signal transduction during T cell development and activation.American journal of clinical and experimental immunology · 2012
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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

3 authors at 1 institution in 1 country.

Minghua ZhuDepartment of Immunology, Duke University, Medical Center, Durham, North Carolina 27710, USA.
Deirdre M Fuller
Weiguo Zhang
Duke Medical Center · US

Funding

Analysis of adaptor protein (LAT) in TCR signalingR01AI048674 · NIAID · DUKE UNIVERSITY · PI ZHANG, WEIGUO · 2001 to 2011
$3.5M
Adaptor molecules in lymphocyte signalingR01AI056156 · NIAID · DUKE UNIVERSITY · PI ZHANG, WEIGUO · 2003 to 2007
$1.5M
Analysis of adaptor protein (LAT) in TCR signalingR56AI048674 · NIAID · DUKE UNIVERSITY · PI ZHANG, WEIGUO · 2012 to 2012
$385k
Adaptor molecules in lymphocyte signalingR56AI056156 · NIAID · DUKE UNIVERSITY · PI ZHANG, WEIGUO · 2010 to 2010
$382k
NIAID NIH HHS AI048674NIAID NIH HHS AI056156NIAID NIH HHS R01 AI048674NIAID NIH HHS R01 AI056156NIAID NIH HHS R56 AI048674NIAID NIH HHS R56 AI056156
6 · The paper itself

Abstract

The RasGRP (Ras guanine nucleotide-releasing protein) family proteins are guanine nucleotide exchange factors that activate Ras GTPases, ultimately leading to MAPK activation and many cellular processes. The RasGRP family has four members. Published studies demonstrate that RasGRP1, RasGRP2, and RasGRP3 play critical roles in T cells, platelets, and B cells, respectively. RasGRP4 is highly expressed in mast cells. Although previous data suggest that it is important in mast cell development and function, the role of RasGRP4 in mast cells and allergic responses has not been clearly demonstrated. In this study, we generated RasGRP4(-/-) mice to examine the function of RasGRP4. Analyses of these mice showed that mast cells were able to develop normally in vivo and in vitro. Despite high levels of RasGRP4 expression in mast cells, RasGRP4 deficiency led to only a modest reduction in FcεRI-mediated degranulation and cytokine production. Interestingly, mast cells deficient in both RasGRP1 and RasGRP4 had a much more severe block in FcεRI-mediated signaling and mast cell function. We also made the unexpected finding that RasGRP4 functions during thymocyte development. Our data suggest that after the engagement of immunoreceptors, immune cells likely employ multiple members of the RasGRP family to transduce critical signals.

Indexed as

AnimalsCell DegranulationGuanine Nucleotide Exchange FactorsHypersensitivityMast CellsMiceMice, Knockoutras Guanine Nucleotide Exchange FactorsReceptors, IgESignal TransductionThymocytesT-LymphocytesGuanine Nucleotide Exchange FactorsRasgrp1 protein, mouseRasgrp4 protein, mouseras Guanine Nucleotide Exchange FactorsReceptors, IgE

Identifiers

PMID22262848
PMCPMC3318739
OpenAlexW1974710413

What OpenQuestion holds

Textmetadata
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.