B-1 Cell Lymphoma in Mice Lacking the Steroid and Xenobiotic Receptor, SXR

被引:15
作者
Casey, Stephanie C. [1 ]
Nelson, Edward L. [2 ,4 ]
Turco, Gina M. [1 ]
Janes, Matthew R. [2 ]
Fruman, David A. [2 ]
Blumberg, Bruce [1 ,3 ]
机构
[1] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Mol Biol & Biochem, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Pharmaceut Sci, Irvine, CA 92697 USA
[4] Univ Calif Irvine, Dept Med, Div Hematol Oncol, Irvine, CA 92697 USA
基金
美国国家卫生研究院;
关键词
NF-KAPPA-B; DISEASE PROGRESSION; NUCLEAR RECEPTORS; PERIPHERAL-BLOOD; GENE-EXPRESSION; LCK; LEUKEMIA; KINASE; INFLAMMATION; METABOLISM;
D O I
10.1210/me.2010-0486
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The steroid and xenobiotic receptor (SXR) is a broad-specificity nuclear hormone receptor that is highly expressed in the liver and intestine, where its primary function is to regulate drug and xenobiotic metabolism. SXR is expressed at lower levels in other tissues, where little is known about its physiological functions. We previously linked SXR with immunity and inflammation by showing that SXR antagonizes the activity of nuclear factor (NF)-kappa B in vitro and in vivo. SXR-/- mice demonstrate aberrantly high NF-kappa B activity and overexpression of NF-kappa B target genes. Here we show that SXR-/- mice develop B cell lymphoma in an age-dependent manner. SXR-/- mice develop multiple hyperplastic lymphoid foci composed of B-1a cells in the intestine, spleen, lymph nodes, peritoneal cavity, and blood. In all circumstances, these lymphocytes possess cell surface and molecular characteristics of either chronic lymphocytic leukemia or non-Hodgkin's lymphoma originating from B-1 lymphocytes. These results demonstrate a novel and unsuspected role for SXR signaling in the B-1 cell compartment, establish SXR as a tumor suppressor in B-1 cells, and may provide a link between metabolism of xenobiotic compounds and lymphomagenesis. (Molecular Endocrinology 25: 933-943, 2011)
引用
收藏
页码:933 / 943
页数:11
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