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E-LettersEditors' Choice:
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Chloride Currents: Don't Forget ClC-3While there is much justified excitement concerning the identification of TMEM16A as a calcium-activated chloride channel (1, 2), I would like to draw attention to the existence of a completely different protein that makes substantial contributions to the transmembrane chloride currents that drive "cell excitability and fluid secretion", as well as many other physiological activities (3). These particular chloride currents also owe their activation to elevations in cytosolic calcium, but indirectly, through the activity of calcium calmodulin kinase II (CaMKII) (4); these chloride currents are also of biological interest because they are inhibited in a receptor-dependent manner by a specific member of the inositol phosphate signaling family (3-6). It is ClC-3 that is responsible for these chloride currents (3); the electrophysiological characteristics of the CaMKII-activated, ClC-3 driven whole-cell currents mirror those of native kinase-activated chloride currents (3-7). The identification of TMEM16A is important, but it's not, as you argue, the "long-sought primary carrier", and neither does its discovery "clinch" the chloride channel field. References
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Science Signaling. ISSN 1937-9145 (online), 1945-0877 (print). Pre-2008: Science's STKE. ISSN 1525-8882