Evidence map›Paper›PMID 18056377›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2007

Rap1a null mice have altered myeloid cell functions suggesting distinct roles for the closely related Rap1a and 1b proteins.

Yu Li, Jingliang Yan, Pradip De, Hua-Chen Chang, Akira Yamauchi, Kent W Christopherson, Nivanka C Paranavitana, Xiaodong Peng, Chaekyun Kim, Veerendra Munugalavadla and 9 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

82 citing papers in PubMed, 117 citations in OpenAlex.

  1. Article
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  10. ArhGEF12 activates Rap1A and not RhoA in human dermal microvascular endothelial cells to reduce tumor necrosis factor-induced leak.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
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  20. Review

22 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
    Munugulavadla, Veerendra [corrected to Munugalavadla, Veerendra]
5 · Who and what money

Authors and funding

19 authors at 8 institutions in 4 countries.

Yu LiDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis 46202, USA.
Jingliang Yan
Pradip De
Hua-Chen Chang
Akira Yamauchi
Kent W Christopherson
Nivanka C Paranavitana
Xiaodong Peng
Chaekyun Kim
Veerendra Munugalavadla
Veerendra Munugulavadla
Reuben Kapur
Hanying Chen
Weinian Shou
James C Stone
Mark H Kaplan
Mary C Dinauer
Donald L Durden
Lawrence A Quilliam
Indiana University School of MedicineWalther Cancer Foundation · USBipar · FREmory University · USInha University · KRPediatrics and Genetics · USRush University Medical Center · USUniversity of Alberta · CA

Funding

Transcriptional regulation of Rac genesP01HL069974 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI SKALNIK, DAVID G · 2002 to 2006
$6.7M
Novel Mechanisms of C-Kit Regulation in Mast CellsR01HL077177 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI KAPUR, REUBEN · 2006 to 2016
$3.0M
Molecular Pathway in Myocardium DevelopmentR01HL081092 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI SHOU, WEINIAN · 2007 to 2011
$1.9M
The Role of BMP-10 in Cardiac DevelopmentR01HL070259 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI SHOU, WEINIAN · 2002 to 2005
$1.3M
Rheb GTPase as chemotherapeutic target for brain tumorsR01CA108647 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI QUILLIAM, LAWRENCE A. · 2005 to 2009
$1.2M
NCI NIH HHS CA108647NCI NIH HHS R01 CA108647NHLBI NIH HHS HL69974NHLBI NIH HHS P01 HL069974NHLBI NIH HHS R01 HL070259NHLBI NIH HHS R01 HL077177NHLBI NIH HHS R01 HL081092
6 · The paper itself

Abstract

The Ras-related GTPases Rap1a and 1b have been implicated in multiple biological events including cell adhesion, free radical production, and cancer. To gain a better understanding of Rap1 function in mammalian physiology, we deleted the Rap1a gene. Although loss of Rap1a expression did not initially affect mouse size or viability, upon backcross into C57BL/6J mice some Rap1a-/- embryos died in utero. T cell, B cell, or myeloid cell development was not disrupted in Rap1a-/- mice. However, macrophages from Rap1a null mice exhibited increased haptotaxis on fibronectin and vitronectin matrices that correlated with decreased adhesion. Chemotaxis of lymphoid and myeloid cells in response to CXCL12 or CCL21 was significantly reduced. In contrast, an increase in FcR-mediated phagocytosis was observed. Because Rap1a was previously copurified with the human neutrophil NADPH oxidase, we addressed whether GTPase loss affected superoxide production. Neutrophils from Rap1a-/- mice had reduced fMLP-stimulated superoxide production as well as a weaker initial response to phorbol ester. These results suggest that, despite 95% amino acid sequence identity, similar intracellular distribution, and broad tissue distribution, Rap1a and 1b are not functionally redundant but rather differentially regulate certain cellular events.

Indexed as

Amino Acid SequenceAnimalsB-LymphocytesChemokine CCL21Chemokine CXCL12ChemotaxisLymphocytesMiceMice, KnockoutMyeloid CellsNeutrophilsPhagocytosisPhorbol Estersrap1 GTP-Binding Proteinsrap GTP-Binding ProteinsRespiratory BurstChemokine CCL21Chemokine CXCL12Phorbol EstersRap1b protein, mouserap1 GTP-Binding Proteinsrap GTP-Binding ProteinsSuperoxides

Identifiers

PMID18056377
PMCPMC2722108
OpenAlexW2096638905

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.