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J Neurosci. July 24, 2013; 33 (30): 12275-86.

CLHM-1 is a functionally conserved and conditionally toxic Ca2+-permeable ion channel in Caenorhabditis elegans.

Tanis JE , Ma Z , Krajacic P , He L , Foskett JK , Lamitina T .

Disruption of neuronal Ca(2+) homeostasis contributes to neurodegenerative diseases through mechanisms that are not fully understood. A polymorphism in CALHM1, a recently described ion channel that regulates intracellular Ca(2+) levels, is a possible risk factor for late-onset Alzheimer''s disease. Since there are six potentially redundant CALHM family members in humans, the physiological and pathophysiological consequences of CALHM1 function in vivo remain unclear. The nematode Caenorhabditis elegans expresses a single CALHM1 homolog, CLHM-1. Here we find that CLHM-1 is expressed at the plasma membrane of sensory neurons and muscles. Like human CALHM1, C. elegans CLHM-1 is a Ca(2+)-permeable ion channel regulated by voltage and extracellular Ca(2+). Loss of clhm-1 in the body-wall muscles disrupts locomotory kinematics and biomechanics, demonstrating that CLHM-1 has a physiologically significant role in vivo. The motility defects observed in clhm-1 mutant animals can be rescued by muscle-specific expression of either C. elegans CLHM-1 or human CALHM1, suggesting that the function of these proteins is conserved in vivo. Overexpression of either C. elegans CLHM-1 or human CALHM1 in neurons is toxic, causing degeneration through a necrotic-like mechanism that is partially Ca(2+) dependent. Our data show that CLHM-1 is a functionally conserved ion channel that plays an important but potentially toxic role in excitable cell function.

PubMed ID: 23884934
PMC ID: PMC3721838
Article link: J Neurosci.
Grant support: F32AR060128 NIAMS NIH HHS , R21 NS072775 NINDS NIH HHS , R21NS072775 NINDS NIH HHS , R21NS072775 NINDS NIH HHS , F32 AR060128 NIAMS NIH HHS , R21 NS072775 NINDS NIH HHS , R01 DC012538 NIDCD NIH HHS , F32AR060128 NIAMS NIH HHS

Genes referenced: calhm1

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