作者
Michael P Lees, Stephen J Fuller, Rima McLeod, Nicola R Boulter, Catherine M Miller, Alana M Zakrzewski, Ernest J Mui, William H Witola, Jessica J Coyne, Aubrey C Hargrave, Sarra E Jamieson, Jenefer M Blackwell, James S Wiley, Nicholas C Smith
发表日期
2010/6/15
期刊
The journal of immunology
卷号
184
期号
12
页码范围
7040-7046
出版商
American Association of Immunologists
简介
The P2X 7 R is highly expressed on the macrophage cell surface, and activation of infected cells by extracellular ATP has been shown to kill intracellular bacteria and parasites. Furthermore, single nucleotide polymorphisms that decrease receptor function reduce the ability of human macrophages to kill Mycobacterium tuberculosis and are associated with extrapulmonary tuberculosis. In this study, we show that macrophages from people with the 1513C (rs3751143, NM_002562. 4: c. 1487A> C) loss-of-function P2X 7 R single nucleotide polymorphism are less effective in killing intracellular Toxoplasma gondii after exposure to ATP compared with macrophages from people with the 1513A wild-type allele. Supporting a P2X 7 R-specific effect on T. gondii, macrophages from P2X 7 R knockout mice (P2X 7 R−/−) are unable to kill T. gondii as effectively as macrophages from wild-type mice. We show that P2X 7 R …
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