Cl- channels are widely found anion pores that are regulated by a variety of signals and that play various roles. On the basis of molecular biologic findings, ligand-gated Cl- channels in synapses, cystic fibrosis transmembrane conductors (CFTRs) and ClC channel types have been established, followed by bestrophin and possibly by tweety, which encode Ca 2+-activated Cl- channels. The ClC family has been shown to possess a variety of functions, including stabilization of membrane potential, excitation, cell-volume regulation, fluid transport, protein degradation in endosomal vesicles and possibly cell growth. The molecular structure of Cl- channel types varies from 1 to 12 transmembrane segments. By means of computer-based prediction, functional Cl- channels have been synthesized artificially, revealing that many possible ion pores are hidden in channel, transporter or unidentified hydrophobic membrane proteins. Thus, novel Cl--conducting pores may be occasionally discovered, and evidence from molecular biologic studies will clarify their physiologic and pathophysiologic roles. © Birkhäuser Verlag, 2006.
CITATION STYLE
Suzuki, M., Morita, T., & Iwamoto, T. (2006, January). Diversity of Cl- channels. Cellular and Molecular Life Sciences. https://doi.org/10.1007/s00018-005-5336-4
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