Romanenko Victor G, Nakamoto Tetsuji, Srivastava Alaka, Begenisich Ted, Melvin James E
Center for Oral Biology in the Aab Institute of Biomedical Sciences and Department of Pharmacology and Physiology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.
J Physiol. 2007 Jun 1;581(Pt 2):801-17. doi: 10.1113/jphysiol.2006.127498. Epub 2007 Mar 22.
We have recently shown that the IK1 and maxi-K channels in parotid salivary gland acinar cells are encoded by the K(Ca)3.1 and K(Ca)1.1 genes, respectively, and in vivo stimulated parotid secretion is severely reduced in double-null mice. The current study tested whether submandibular acinar cell function also relies on these channels. We found that the K(+) currents in submandibular acinar cells have the biophysical and pharmacological footprints of IK1 and maxi-K channels and their molecular identities were confirmed by the loss of these currents in K(Ca)3.1- and K(Ca)1.1-null mice. Unexpectedly, the pilocarpine-stimulated in vivo fluid secretion from submandibular glands was essentially normal in double-null mice. This result and the possibility of side-effects of pilocarpine on the nervous system, led us to develop an ex vivo fluid secretion assay. Fluid secretion from the ex vivo assay was substantially (about 75%) reduced in animals with both K(+) channel genes ablated - strongly suggesting systemic complications with the in vivo assay. Additional experiments focusing on the membrane potential in isolated submandibular acinar cells revealed mechanistic details underlying fluid secretion in K(+) channel-deficient mice. The membrane potential of submandibular acinar cells from wild-type mice remained strongly hyperpolarized (-55 +/- 2 mV) relative to the Cl(-) equilibrium potential (-24 mV) during muscarinic stimulation. Similar hyperpolarizations were observed in K(Ca)3.1- and K(Ca)1.1-null mice (-51 +/- 3 and -48 +/- 3 mV, respectively), consistent with the normal fluid secretion produced ex vivo. In contrast, acinar cells from double K(Ca)3.1/K(Ca)1.1-null mice were only slightly hyperpolarized (-35 +/- 2 mV) also consistent with the ex vivo (but not in vivo) results. Finally, we found that the modest hyperpolarization of cells from the double-null mice was maintained by the electrogenic Na(+),K(+)-ATPase.
我们最近发现,腮腺腺泡细胞中的IK1和大电导钙激活钾通道分别由K(Ca)3.1和K(Ca)1.1基因编码,在双基因敲除小鼠中,体内刺激的腮腺分泌严重减少。当前的研究测试了下颌下腺泡细胞功能是否也依赖于这些通道。我们发现,下颌下腺泡细胞中的钾电流具有IK1和大电导钙激活钾通道的生物物理和药理学特征,并且在K(Ca)3.1和K(Ca)1.1基因敲除小鼠中这些电流的消失证实了它们的分子身份。出乎意料的是,毛果芸香碱刺激的下颌下腺体内液体分泌在双基因敲除小鼠中基本正常。这一结果以及毛果芸香碱对神经系统产生副作用的可能性,促使我们开发一种离体液体分泌检测方法。在两种钾通道基因均被敲除的动物中,离体检测的液体分泌大幅减少(约75%),这强烈表明体内检测存在系统性并发症。聚焦于分离的下颌下腺泡细胞膜电位的额外实验揭示了钾通道缺陷小鼠中液体分泌的潜在机制细节。在毒蕈碱刺激期间,野生型小鼠下颌下腺泡细胞的膜电位相对于氯离子平衡电位(-24 mV)仍保持强烈超极化(-55±2 mV)。在K(Ca)3.1和K(Ca)1.1基因敲除小鼠中也观察到类似的超极化(分别为-51±3 mV和-48±3 mV),这与离体产生的正常液体分泌一致。相比之下,双基因敲除小鼠(K(Ca)3.1/K(Ca)1.1)的腺泡细胞仅轻微超极化(-35±2 mV),这也与离体(而非体内)结果一致。最后,我们发现双基因敲除小鼠细胞的适度超极化是由电生性钠钾ATP酶维持 的。