Park Channy, Kalinec Federico
Laboratory of Auditory Cell Biology, Department of Head & Neck Surgery, David Geffen School of Medicine at UCLA, Los Angeles, California.
Laboratory of Auditory Cell Biology, Department of Head & Neck Surgery, David Geffen School of Medicine at UCLA, Los Angeles, California.
Biophys J. 2015 May 5;108(9):2171-80. doi: 10.1016/j.bpj.2015.03.044.
There is strong evidence that changes in the actin/spectrin-based cortical cytoskeleton of outer hair cells (OHCs) regulate their motile responses as well as cochlear amplification, the process that optimizes the sensitivity and frequency selectivity of the mammalian inner ear. Since a RhoA/protein kinase C (PKC)-mediated pathway is known to inhibit the actin-spectrin interaction in other cell models, we decided to investigate whether this signaling cascade could also participate in the regulation of OHC motility. We used high-speed video microscopy and confocal microscopy to explore the effects of pharmacological activation of PKCα, PKCβI, PKCβII, PKCδ, PKCε, and PKCζ with lysophosphatidic acid (LPA) and their inhibition with bisindolylmaleimide I, as well as inhibition of RhoA and Rho-associated protein kinase (ROCK) with C3 and Y-27632, respectively. Motile responses were induced in isolated guinea pig OHCs by stimulation with an 8 V/cm external alternating electrical field as 50 Hz bursts of square wave pulses (100 ms on/off). We found that LPA increased expression of PKCα and PKCζ only, with PKCα, but not PKCζ, phosphorylating the cytoskeletal protein adducin of both Ser-726 and Thr-445. Interestingly, however, inhibition of PKCα reduced adducin phosphorylation only at Ser-726. We also determined that LPA activation of a PKCα-mediated signaling pathway simultaneously enhanced OHC electromotile amplitude and cell shortening, and facilitated RhoA/ROCK/LIMK1-mediated cofilin phosphorylation. Altogether, our results suggest that PKCα-mediated signals, probably via adducin-mediated inhibition of actin-spectrin binding and cofilin-mediated depolymerization of actin filaments, play an essential role in the homeostatic regulation of OHC motility and cochlear amplification.
有强有力的证据表明,外毛细胞(OHCs)基于肌动蛋白/血影蛋白的皮质细胞骨架的变化调节其运动反应以及耳蜗放大,耳蜗放大是优化哺乳动物内耳敏感性和频率选择性的过程。由于已知RhoA/蛋白激酶C(PKC)介导的途径在其他细胞模型中抑制肌动蛋白-血影蛋白相互作用,我们决定研究该信号级联是否也参与OHC运动的调节。我们使用高速视频显微镜和共聚焦显微镜来探究溶血磷脂酸(LPA)对PKCα、PKCβI、PKCβII、PKCδ、PKCε和PKCζ的药理学激活作用及其被双吲哚马来酰亚胺I抑制的效果,以及分别用C3和Y-27632对RhoA和Rho相关蛋白激酶(ROCK)的抑制作用。通过用8V/cm的外部交变电场以50Hz的方波脉冲串(开/关100ms)刺激,在分离的豚鼠OHC中诱导运动反应。我们发现LPA仅增加PKCα和PKCζ的表达,其中PKCα而非PKCζ使细胞骨架蛋白内收蛋白的Ser-726和Thr-445位点磷酸化。然而,有趣的是,抑制PKCα仅降低内收蛋白在Ser-726位点的磷酸化。我们还确定LPA激活PKCα介导的信号通路同时增强了OHC电运动幅度和细胞缩短,并促进了RhoA/ROCK/LIMK1介导的丝切蛋白磷酸化。总之,我们的结果表明,PKCα介导的信号可能通过内收蛋白介导的肌动蛋白-血影蛋白结合抑制和丝切蛋白介导的肌动蛋白丝解聚,在OHC运动和耳蜗放大的稳态调节中起重要作用。