Expression analysis of the ligands for the Natural Killer cell receptors NKp30 and NKp44.

BACKGROUND: The natural cytotoxicity receptors (NCR) are important to stimulate the activity of Natural Killer (NK) cells against transformed cells. Identification of NCR ligands and their level of expression on normal and neoplastic cells has important implications for the rational design of immun...

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Main Authors: Andreina Byrd, Sabrina C Hoffmann, Mostafa Jarahian, Frank Momburg, Carsten Watzl
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2007-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2129109?pdf=render
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spelling doaj-96e8b2f2d6474f50968b95feb041da902020-11-25T02:01:21ZengPublic Library of Science (PLoS)PLoS ONE1932-62032007-01-01212e133910.1371/journal.pone.0001339Expression analysis of the ligands for the Natural Killer cell receptors NKp30 and NKp44.Andreina ByrdSabrina C HoffmannMostafa JarahianFrank MomburgCarsten Watzl BACKGROUND: The natural cytotoxicity receptors (NCR) are important to stimulate the activity of Natural Killer (NK) cells against transformed cells. Identification of NCR ligands and their level of expression on normal and neoplastic cells has important implications for the rational design of immunotherapy strategies for cancer. METHODOLOGY/PRINCIPAL FINDINGS: Here we analyze the expression of NKp30 ligand and NKp44 ligand on 30 transformed or non-transformed cell lines of different origin. We find intracellular and surface expression of these two ligands on almost all cell lines tested. Expression of NKp30 and NKp44 ligands was variable and did not correlate with the origin of the cell line. Expression of NKp30 and NKp44 ligand correlated with NKp30 and NKp44-mediated NK cell lysis of tumor cells, respectively. The surface expression of NKp30 ligand and NKp44 ligand was sensitive to trypsin treatment and was reduced in cells arrested in G(2)/M phase. CONCLUSION/SIGNIFICANCE: These data demonstrate the ubiquitous expression of the ligands for NKp30 and NKp44 and give an important insight into the regulation of these ligands.http://europepmc.org/articles/PMC2129109?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Andreina Byrd
Sabrina C Hoffmann
Mostafa Jarahian
Frank Momburg
Carsten Watzl
spellingShingle Andreina Byrd
Sabrina C Hoffmann
Mostafa Jarahian
Frank Momburg
Carsten Watzl
Expression analysis of the ligands for the Natural Killer cell receptors NKp30 and NKp44.
PLoS ONE
author_facet Andreina Byrd
Sabrina C Hoffmann
Mostafa Jarahian
Frank Momburg
Carsten Watzl
author_sort Andreina Byrd
title Expression analysis of the ligands for the Natural Killer cell receptors NKp30 and NKp44.
title_short Expression analysis of the ligands for the Natural Killer cell receptors NKp30 and NKp44.
title_full Expression analysis of the ligands for the Natural Killer cell receptors NKp30 and NKp44.
title_fullStr Expression analysis of the ligands for the Natural Killer cell receptors NKp30 and NKp44.
title_full_unstemmed Expression analysis of the ligands for the Natural Killer cell receptors NKp30 and NKp44.
title_sort expression analysis of the ligands for the natural killer cell receptors nkp30 and nkp44.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2007-01-01
description BACKGROUND: The natural cytotoxicity receptors (NCR) are important to stimulate the activity of Natural Killer (NK) cells against transformed cells. Identification of NCR ligands and their level of expression on normal and neoplastic cells has important implications for the rational design of immunotherapy strategies for cancer. METHODOLOGY/PRINCIPAL FINDINGS: Here we analyze the expression of NKp30 ligand and NKp44 ligand on 30 transformed or non-transformed cell lines of different origin. We find intracellular and surface expression of these two ligands on almost all cell lines tested. Expression of NKp30 and NKp44 ligands was variable and did not correlate with the origin of the cell line. Expression of NKp30 and NKp44 ligand correlated with NKp30 and NKp44-mediated NK cell lysis of tumor cells, respectively. The surface expression of NKp30 ligand and NKp44 ligand was sensitive to trypsin treatment and was reduced in cells arrested in G(2)/M phase. CONCLUSION/SIGNIFICANCE: These data demonstrate the ubiquitous expression of the ligands for NKp30 and NKp44 and give an important insight into the regulation of these ligands.
url http://europepmc.org/articles/PMC2129109?pdf=render
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