You are not currently logged in.
Access your personal account or get JSTOR access through your library or other institution:
If You Use a Screen ReaderThis content is available through Read Online (Free) program, which relies on page scans. Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.
Defective membrane expression of the Na + -HCO 3 − cotransporter NBCe1 is associated with familial migraine
Masashi Suzuki, Wim Van Paesschen, Ingeborg Stalmans, Shoko Horita, Hideomi Yamada, Bruno A. Bergmans, Eric Legius, Florence Riant, Peter De Jonghe, Yuehong Li, Takashi Sekine, Takashi Igarashi, Ichiro Fujimoto, Katsuhiko Mikoshiba, Mitsunobu Shimadzu, Masaaki Shiohara, Nancy Braverman, Lihadh Al-Gazali, Toshiro Fujita, George Seki and Michael J. Welsh
Proceedings of the National Academy of Sciences of the United States of America
Vol. 107, No. 36 (September 7, 2010), pp. 15963-15968
Published by: National Academy of Sciences
Stable URL: http://www.jstor.org/stable/27862365
Page Count: 6
Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.
Preview not available
Homozygous mutations is SLC4A4, encoding the electrogenic Na + -HCO 3 − cotransporter NBCe1, have been known to cause proximal renal tubular acidosis (pRTA) and ocular abnormalities. In this study, we report two sisters with pRTA, ocular abnormalities, and hemiplegic migraine. Genetic analysis ruled out pathological mutations in the known genes for familial hemiplegic migraine, but identified a homozygous 65-bp deletion (Δ65bp) in the C terminus of NBCe1, corresponding to the codon change S982NfsX4. Several heterozygous members of this family also presented glaucoma and migraine with or without aura. Despite the normal electrogenic activity in Xenopus oocytes, the Δ65bp mutant showed almost no transport activity due to a predominant cytosolic retention in mammalian cells. Furthermore, coexpression experiments uncovered a dominant negative effect of the mutant through hetero-oligomer formation with wild-type NBCe1. Among other pRTA pedigrees with different NBCe1 mutations, we identified four additional homozygous patients with migraine. The immunohistological and functional analyses of these mutants demonstrate that the near total loss of NBCe1 activity in astrocytes can cause migraine potentially through dysregulation of synaptic pH.
Proceedings of the National Academy of Sciences of the United States of America © 2010 National Academy of Sciences