Correolide and derivatives are novel immunosuppressants blocking the lymphocyte Kv1.3 potassium channels

被引:82
作者
Koo, GC
Blake, JT
Shah, K
Staruch, MJ
Dumont, F
Wunderler, D
Sanchez, M
McManus, OB
Sirotina-Meisher, A
Fischer, P
Boltz, RC
Goetz, MA
Baker, R
Bao, JM
Kayser, F
Rupprecht, KM
Parsons, WH
Tong, XC
Ita, IE
Pivnichny, J
Vincent, S
Cunningham, P
Hora, D
Feeney, W
Kaczorowski, G
Springer, MS
机构
[1] Merck Res Labs, Dept Immunol Res, Rahway, NJ 07065 USA
[2] Merck Res Labs, Dept Nat Prod Drug Discovery, Rahway, NJ 07065 USA
[3] Merck Res Labs, Dept Med Chem, Rahway, NJ 07065 USA
[4] Merck Res Labs, Dept Drug Metab, Rahway, NJ 07065 USA
[5] Merck Res Labs, Dept Membrane Biochem & Biophys, Rahway, NJ 07065 USA
[6] Merck Res Labs, Dept Lab Anim Resources, Rahway, NJ 07065 USA
关键词
D O I
10.1006/cimm.1999.1569
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The voltage-gated potassium channel, Kv1.3, is specifically expressed on human lymphocytes, where it controls membrane potential and calcium influx. Blockade of Kv1.3 channels by margatoxin was previously shown to prevent T cell activation and attenuate immune responses in vivo. In the present study, a triterpene natural product, correolide, was found to block Kv1.3 channels in human and miniswine T cells by electrophysiological characterization. T cell activation events, such as anti-CD3-induced calcium elevation, IL-2 production, and proliferation were inhibited by correolide in a dose-dependent manner. More potent analogs were evaluated for pharmacokinetic profiles and subsequently tested in a delayed-type hypersensitivity (DTH) response to tuberculin in the miniswine. Two compounds were dosed orally, iv, or im, and both compounds suppressed DTH responses, demonstrating that small molecule blockers of Kv1.3 channels can act as immunosuppressive agents in vivo. These studies establish correolide and its derivatives as novel immunosuppressants. (C) 1999 Academic Press.
引用
收藏
页码:99 / 107
页数:9
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