Format

Send to

Choose Destination
PLoS One. 2013 Jun 3;8(6):e63193. doi: 10.1371/journal.pone.0063193. Print 2014.

In TCR-stimulated T-cells, N-ras regulates specific genes and signal transduction pathways.

Author information

1
Department of Pathology, New York University Langone School of Medicine, New York, New York, United States of America.

Erratum in

  • PLoS One. 2013;8(9). doi:10.1371/annotation/f0d2b6b0-7d87-492e-8505-5159c4b5bdd5.

Abstract

It has been recently shown that N-ras plays a preferential role in immune cell development and function; specifically: N-ras, but not H-ras or K-ras, could be activated at and signal from the Golgi membrane of immune cells following a low level T-cell receptor stimulus. The goal of our studies was to test the hypothesis that N-ras and H-ras played distinct roles in immune cells at the level of the transcriptome. First, we showed via mRNA expression profiling that there were over four hundred genes that were uniquely differentially regulated either by N-ras or H-ras, which provided strong evidence in favor of the hypothesis that N-ras and H-ras have distinct functions in immune cells. We next characterized the genes that were differentially regulated by N-ras in T cells following a low-level T-cell receptor stimulus. Of the large pool of candidate genes that were differentially regulated by N-ras downstream of TCR ligation, four genes were verified in qRT-PCR-based validation experiments (Dntt, Slc9a6, Chst1, and Lars2). Finally, although there was little overlap between individual genes that were regulated by N-ras in unstimulated thymocytes and stimulated CD4(+) T-cells, there was a nearly complete correspondence between the signaling pathways that were regulated by N-ras in these two immune cell types.

PMID:
23755101
PMCID:
PMC3670928
DOI:
10.1371/journal.pone.0063193
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Public Library of Science Icon for PubMed Central
Loading ...
Support Center