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LILRB1 polymorphism and surface phenotypes of natural killer cells. | LitMetric

LILRB1 polymorphism and surface phenotypes of natural killer cells.

Hum Immunol

Department of Medical Microbiology and Immunology, University of Alberta, Edmonton, Alberta, Canada.

Published: October 2010

AI Article Synopsis

  • LIR-1 is an inhibitory receptor that can bind various class I HLA molecules and is encoded by the LILRB1 gene, showing consistent expression on monocytes and B cells, but varying levels on NK cells among individuals.
  • The study analyzed the relationship between genetic variations in the LILRB1 gene and NK cell expression levels, revealing that certain SNPs are linked to higher expression of LIR-1 on NK cells.
  • Findings indicate significant diversity in the LILRB1 locus, which may impact individual immune responses by influencing LIR-1 expression on NK cells.

Article Abstract

Leukocyte Ig-like receptor (LIR)-1 is an inhibitory receptor that binds a broad range of class I HLA molecules and is encoded by the LILRB1 gene within the leukocyte receptor complex. In contrast to uniform expression on monocytes and B cells, LIR-1 expression on natural killer (NK) cells varies considerably between individuals. To investigate how polymorphism is related to the observed patterns of expression, we analyzed the LILRB1 gene and its transcriptional activity in a group of individuals with various levels of expression on NK cells. We found that LILRB1 transcription is correlated with surface protein expression on NK cells. In a cohort of 24 donors, we found high expression on NK cells to be associated with three linked SNPs (AGG verses GAA) within the putative regulatory region. We also identified several new protein variants and observed variants with P, T, T, and I at positions 68, 95, 142, and 155, respectively, more frequently in donors with low expression on NK cells. These results suggest that there is a significant degree of diversity within the LILRB1 locus and that it influences expression patterns on NK cells. These genetic differences may underpin variation in individual immune responses involving LIR-1 on NK cells.

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Source
http://dx.doi.org/10.1016/j.humimm.2010.06.015DOI Listing

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