Abstract.
Gap junctions (GJs) are composed of proteins that form a channel connecting the cytoplasm of adjacent cells. Connexins were initially considered to be the only proteins capable of GJ formation. Another family of GJ proteins (innexins) were first found in invertebrates and were proposed to be renamed pannexins after their orthologs were discovered in vertebrates. The lack of both connexins and pannexins in the genomes of some metazoans suggests that other, still undiscovered GJ proteins exist. In vertebrates, connexins and pannexins co-exist. Here we discuss whether vertebrate pannexins have a nonredundant role in animal physiology. Pannexin channels appear to be suited for ATP and calcium signaling and play a role in the maintenance of calcium homeostasis by mechanisms implicating both GJ and nonjunctional function. Suggested roles in the ischemic death of neurons, schizophrenia, inflammation and tumor suppression have drawn much attention to exploring the molecular properties and cellular functions of pannexins.
Similar content being viewed by others
Author information
Authors and Affiliations
Corresponding author
Additional information
Received 22 April 2007; received after revision 9 September 2007; accepted 19 September 2007
Rights and permissions
About this article
Cite this article
Shestopalov, V.I., Panchin, Y. Pannexins and gap junction protein diversity. Cell. Mol. Life Sci. 65, 376–394 (2008). https://doi.org/10.1007/s00018-007-7200-1
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00018-007-7200-1