Bukiya Anna N, McMillan Jacob, Liu Jianxi, Shivakumar Bangalore, Parrill Abby L, Dopico Alex M
From the Department of Pharmacology, University of Tennessee Health Science Center, Memphis, Tennessee 38163 and
the Department of Chemistry and Computational Research on Materials Institute (CROMIUM), University of Memphis, Memphis, Tennessee 38152.
J Biol Chem. 2014 Dec 19;289(51):35314-25. doi: 10.1074/jbc.M114.577825. Epub 2014 Nov 4.
Calcium/voltage-gated, large conductance potassium (BK) channels control numerous physiological processes, including myogenic tone. BK channel regulation by direct interaction between lipid and channel protein sites has received increasing attention. Leukotrienes (LTA4, LTB4, LTC4, LTD4, and LTE4) are inflammatory lipid mediators. We performed patch clamp studies in Xenopus oocytes that co-expressed BK channel-forming (cbv1) and accessory β1 subunits cloned from rat cerebral artery myocytes. Leukotrienes were applied at 0.1 nm-10 μm to either leaflet of cell-free membranes at a wide range of [Ca(2+)]i and voltages. Only LTB4 reversibly increased BK steady-state activity (EC50 = 1 nm; Emax reached at 10 nm), with physiological [Ca(2+)]i and voltages favoring this activation. Homomeric cbv1 or cbv1-β2 channels were LTB4-resistant. Computational modeling predicted that LTB4 docked onto the cholane steroid-sensing site in the BK β1 transmembrane domain 2 (TM2). Co-application of LTB4 and cholane steroid did not further increase LTB4-induced activation. LTB4 failed to activate β1 subunit-containing channels when β1 carried T169A, A176S, or K179I within the docking site. Co-application of LTB4 with LTA4, LTC4, LTD4, or LTE4 suppressed LTB4-induced activation. Inactive leukotrienes docked onto a portion of the site, probably preventing tight docking of LTB4. In summary, we document the ability of two endogenous lipids from different chemical families to share their site of action on a channel accessory subunit. Thus, cross-talk between leukotrienes and cholane steroids might converge on regulation of smooth muscle contractility via BK β1. Moreover, the identification of LTB4 as a highly potent ligand for BK channels is critical for the future development of β1-specific BK channel activators.
钙/电压门控的大电导钾(BK)通道控制着众多生理过程,包括肌源性张力。脂质与通道蛋白位点之间的直接相互作用对BK通道的调节作用日益受到关注。白三烯(LTA4、LTB4、LTC4、LTD4和LTE4)是炎症性脂质介质。我们在非洲爪蟾卵母细胞中进行了膜片钳研究,这些卵母细胞共表达了从大鼠脑动脉肌细胞克隆的BK通道形成亚基(cbv1)和辅助β1亚基。在广泛的细胞内钙离子浓度([Ca(2+)]i)和电压条件下,将白三烯以0.1纳米至10微米的浓度施加于无细胞膜的任一表面。只有LTB4能可逆地增加BK的稳态活性(半数有效浓度(EC50) = 1纳米;在10纳米时达到最大效应(Emax)),生理条件下的[Ca(2+)]i和电压有利于这种激活作用。同型cbv1或cbv1-β2通道对LTB4不敏感。计算模型预测LTB4对接在BKβ1跨膜结构域2(TM2)中的胆烷类固醇传感位点上。同时施加LTB4和胆烷类固醇不会进一步增强LTB4诱导的激活作用。当β1在对接位点携带T169A、A176S或K179I时,LTB4无法激活含β1亚基的通道。同时施加LTB4与LTA4、LTC4、LTD4或LTE4会抑制LTB4诱导的激活作用。无活性的白三烯对接在该位点的一部分,可能阻止了LTB4的紧密对接。总之,我们证明了来自不同化学家族的两种内源性脂质能够共享它们在通道辅助亚基上的作用位点。因此,白三烯与胆烷类固醇之间的相互作用可能通过BKβ1汇聚于对平滑肌收缩性的调节。此外,将LTB4鉴定为BK通道的高效配体对于未来β1特异性BK通道激活剂的开发至关重要。