摘要
X-linked Charcot-Marie-Tooth disease is one of a set of diseases caused by mutations in gap junction proteins called connexins. We identified a connexin32 missense mutation (F235C) in a girl with unusually severe neuropathy. The locali zation and trafficking of the mutant protein in cell culture was normal, but electrophysiological studies showed that the mutation caused abnormal hemichannel opening, with excessive permeability of the plasma membrane and decreased cell su rvival. Abnormal leakiness of connexin hemichannels is likely a mechanism of cel lular toxicity in this and perhaps other diseases caused by connexin mutations.
X-linked Charcot-Marie-Tooth disease is one of a set of diseases caused by mutations in gap junction proteins called connexins. We identified a connexin32 missense mutation (F235C) in a girl with unusually severe neuropathy. The locali zation and trafficking of the mutant protein in cell culture was normal, but electrophysiological studies showed that the mutation caused abnormal hemichannel opening, with excessive permeability of the plasma membrane and decreased cell su rvival. Abnormal leakiness of connexin hemichannels is likely a mechanism of cel lular toxicity in this and perhaps other diseases caused by connexin mutations.
出处
《世界核心医学期刊文摘（神经病学分册）》
2005年第9期11-11,共1页
Digest of the World Core Medical Journals:Clinical Neurology
