The voltage-gated potassium channel Kv1.3 is highly expressed on inflammatory infiltrates in multiple sclerosis brain

被引:156
作者
Rus, H
Pardo, CA
Hu, LN
Darrah, E
Cudrici, C
Niculescu, T
Niculescu, F
Mullen, KM
Allie, R
Guo, LP
Wulff, H
Beeton, C
Judge, SIV
Kerr, DA
Knaus, HG
Chandy, KG
Calabresi, PA
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21287 USA
[2] Univ Maryland, Sch Med, Dept Neurol, Baltimore, MD 21201 USA
[3] Vet Affairs Maryland Hlth Care Syst, Multiple Sclerosis Ctr Excellence, Baltimore, MD 21201 USA
[4] Univ Maryland, Sch Med, Dept Med, Div Clin Immunol & Rheumatol, Baltimore, MD 21201 USA
[5] Univ Calif Davis, Dept Med Pharmacol & Toxicol, Davis, CA 95616 USA
[6] Univ Calif Irvine, Dept Physiol, Irvine, CA 92697 USA
[7] Med Univ Innsbruck, Div Mol & Cellular Pharmacol, A-6020 Innsbruck, Austria
关键词
lymphocytes; macrophages; cerebrospinal fluid; effector memory;
D O I
10.1073/pnas.0501770102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Multiple Sclerosis (MS) is characterized by central nervous system perivenular and parenchymal mononuclear cell infiltrates consisting of activated T cells and macrophages. We recently demonstrated that elevated expression of the voltage-gated potassium channel, Kv1.3, is a functional marker of activated effector memory T (T-EM) cells in experimental allergic encephalomyelitis and in myelin-specific T cells derived from the peripheral blood of patients with MS. Herein, we show that Kv1.3 is highly expressed in postmortem MS brain inflammatory infiltrates. The expression pattern revealed not only Kv1.3(+) T cells in the perivenular infiltrate but also high expression in the parenchyma of demyelinated MS lesions and both normal appearing gray and white matter. These cells were uniformly chemokine receptor 7 negative (CCR7(-)), consistent with an effector memory phenotype. Using double-labeling immunohistochemistry and confocal microscopy, we demonstrated colocalization of Kv1.3 with CD3, CD4, CD8, and some CD68 cells. The expression patterns mirrored in vitro experiments showing polarization of Kv1.3 to the immunological synapse. Kv1.3 was expressed in low to moderate levels on CCR7(+) central memory T cells from cerebrospinal fluid, but, when these cells were stimulated in vitro, they rapidly became Kv1.3(high)/CCR7-T-EM, suggesting that a subset of cerebrospinal fluid cells existed in a primed state ready to become TEM. These studies provide further rationale for the use of specific Kv1.3 antagonists in MS.
引用
收藏
页码:11094 / 11099
页数:6
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