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Korean J Physiol Pharmacol
2013 Jun 01;173:223-8. doi: 10.4196/kjpp.2013.17.3.223.
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Activation of lysophosphatidic Acid receptor is coupled to enhancement of ca(2+)-activated potassium channel currents.
Choi SH
,
Lee BH
,
Kim HJ
,
Hwang SH
,
Lee SM
,
Nah SY
.
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The calcium-activated K(+) (BKCa) channel is one of the potassium-selective ion channels that are present in the nervous and vascular systems. Ca(2+) is the main regulator of BKCa channel activation. The BKCa channel contains two high affinity Ca(2+) binding sites, namely, regulators of K(+) conductance, RCK1 and the Ca(2+) bowl. Lysophosphatidic acid (LPA, 1-radyl-2-hydroxy-sn-glycero-3-phosphate) is one of the neurolipids. LPA affects diverse cellular functions on many cell types through G protein-coupled LPA receptor subtypes. The activation of LPA receptors induces transient elevation of intracellular Ca(2+) levels through diverse G proteins such as Gαq/11, Gαi, Gα12/13, and Gαs and the related signal transduction pathway. In the present study, we examined LPA effects on BKCa channel activity expressed in Xenopus oocytes, which are known to endogenously express the LPA receptor. Treatment with LPA induced a large outward current in a reversible and concentration-dependent manner. However, repeated treatment with LPA induced a rapid desensitization, and the LPA receptor antagonist Ki16425 blocked LPA action. LPA-mediated BKCa channel activation was also attenuated by the PLC inhibitor U-73122, IP3 inhibitor 2-APB, Ca(2+) chelator BAPTA, or PKC inhibitor calphostin. In addition, mutations in RCK1 and RCK2 also attenuated LPA-mediated BKCa channel activation. The present study indicates that LPA-mediated activation of the BKCa channel is achieved through the PLC, IP3, Ca(2+), and PKC pathway and that LPA-mediated activation of the BKCa channel could be one of the biological effects of LPA in the nervous and vascular systems.
Fig. 1. Schematic transmembrane diagram of the BKCa channel in the plasma membrane and the LPA chemical structure. (A) There are 7 transmembrane domains along with the RCK1 and RCK2 domains. The voltage sensor and pore of the BKCa channel resembles the responding regions of other voltage-dependent K+ channels (Yuan et al., 2010). Amino acid residues underlined and marked (*) indicate mutation sites in this study. (B) The chemical structure of lysophosphatidic acid (LPA, C18:1).
Fig. 2. Concentration- and voltage-dependent activation of the BKCa channel by LPA in Xenopus oocytes expressing rat brain BKCa channels. (A) The BKCa channel activation by LPA is concentration-dependent. (a) Representative traces of BKCa channel current enhancements using different concentrations of LPA (up to 1 µM). (b) The summary histogram shows the effects of various concentrations of LPA on the BKCa channels. (B) A representative control and LPA-mediated current in an I~V relationship. (a) Currents were recorded at a test potential from -70 to +60 mV, applied from a holding potential of -80 mV. (b) Current-voltage (I-V) relationship of the BKCa channel in the absence (â) or presence (â) of 100 nM LPA. Voltage pulses with 400-ms duration were applied in 10 mV increments at 3-s intervals from a holding potential of -80 mV. The current peaks, normalized to the peak current evoked by the voltage step to +60 mV in the absence of LPA, were used in the I-V plot. Data represent the mean±S.E.M. (n=4).
Fig. 3. Effects of repeated treatments of LPA and LPA1/3 receptor antagonist Ki16425 on LPA-mediated BKCa channel activation. (A-a) Repeated application of 100 nM LPA desensitized the BKCa channel activation with indicated time interval in representative oocyte (left panel). (A-b) The representative BKCa channel current traces by repeated LPA treatments were obtained from timecurrent relationship of "a" (right panel). Outward currents are caused by stepping from -80 mV to +40 mV for 400 ms. Data represent the mean±S.E.M. (n=5). (B-a) Representative traces are from the LPA channel activation in the absence (upper trace) or presence of 10 µM Ki16425 for 10 min (lower trace). (B-b) Summary histogram of the LPA effects on BKCa channel activation (right panel). Data represent the mean±S.E.M. (n=10~12; *p<0.01).
Fig. 4. Signaling pathway of LPA-mediated BKCa channel activation. (A) Effects of the PLC inhibitor on LPA-mediated BKCa channel activation. (a~c) A representative trace shows the activation of LPA-(100 nM) mediated currents in Xenopus oocytes expressing the BKCa channel in the absence or presence of inactive U73343 (1 µM) or active PLC inhibitor U73122 (1 µM). (d) Summary histograms of LPA-mediated activation on control, U-73122, or U-73343-treated groups (right lower panel). Data represent the mean±S.E.M. (n=10~11; *p<0.01). (B) Effect of IP3 receptor antagonist 2-APB on LPA-mediated (100 nM) BKCa channel activation. (a) Representative trace shows the activation of LPA-mediated (100 nM) currents in Xenopus oocytes expressing the BKCa channel in the absence or presence of 100 µM 2-APB for 20 min. (b) Summary histograms of LPA-mediated activation on control or 100 µM 2-APB (right lower panel). Data represent the mean±S.E.M. (n=12~14; *p<0.05). (C) Effect of intracellular Ca2+ chelator, BAPTA-AM, on LPA-mediated (100 nM) BKCa channel activation. (a) A representative trace shows the activation of LPA-mediated (100 nM) currents in Xenopus oocytes expressing the BKCa channel in the absence or presence of BAPTA-AM for 3 h. (b) Summary histograms of LPA-mediated activation on control or 100 µM BAPTA-AM (right lower panel). Data represent the mean±S.E.M. (n=10~12; *p<0.01).
Fig. 5. Effects of PKC inhibitor and mutations in RCK1 and the Ca2+ bowl on LPA-mediated BKCa channel activation. (A-a) Effects of PKC inhibitor on LPA-mediated BKCa channel activation. A representative trace shows the activation of LPA-mediated (100 nM) currents in Xenopus oocytes expressing the BKCa channel in the absence or presence of 1.5 µM calphostin for 2 h. (A-b) Summary histograms of LPA-mediated BKCa channel activation in controls or with 1.5 µM calphostin (right lower panel). Data represent the mean±S.E.M. (n=10~12; *p<0.01). (B) Effect of mutations on the RCK1 and Ca2+ bowl domains in LPA-mediated BKCa channel activation. (B-a) The oocytes expressing wild-type or mutant BKCa channels in the RCK domain such as D433A or M579I were treated with LPA by a bathing application for 60 s. Mutations in the RCK domain attenuated the LPA concentration-responses (left panel). (B-b) The oocytes expressing wild-type or mutant BKCa channels in the Ca2+ bowl were treated with LPA by a bathing application for 60 s. Mutations in the Ca2+ bowl also attenuated LPA concentration-responses (right panel). Data represent the mean±S.E.M. (n=6).
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