[
Exp Parasitol,
1976]
By employing a histochemical procedure on adult nematodes, the base of the Caenorhabditis elegans amphid appears to contain acetylcholinesterase and a nonspecific cholinesterase. Some precipitation was observed in the kinetosome region of the inner labial papilla with acethylthiocholine (AtCh) as substrate but not, in limited observations, in the absence of substrate or with butyrylthiocholine (BtCh). The amphidial tips, the tips of the inner labial papillae, and the lining of the buccal cavity contained substantial reaction product at the ultrastructural level, with or without substrates and inhibitors and therefore cannot be related to the presence of a cholinesterase.
Li Y, Yang Y, Liu Y, Zhang B, Tang TS, Yu J, Tan H, Chen Q, Wang H, Yang M, Wang X, Zheng Q, Li X, Zhou A, Guo C, Wang F, Wang JQ, Chai H, Sun Z, Wang QC, Zhu S
[
Cell,
2016]
Maintaining homeostasis of Ca(2+) stores in the endoplasmic reticulum (ER) is crucial for proper Ca(2+) signaling and key cellular functions. The Ca(2+)-release-activated Ca(2+) (CRAC) channel is responsible for Ca(2+) influx and refilling after store depletion, but how cells cope with excess Ca(2+) when ER stores are overloaded is unclear. We show that TMCO1 is an ER transmembrane protein that actively prevents Ca(2+) stores from overfilling, acting as what we term a "Ca(2+) load-activated Ca(2+) channel" or "CLAC" channel. TMCO1 undergoes reversible homotetramerization in response to ER Ca(2+) overloading anddisassembly upon Ca(2+) depletion and forms a Ca(2+)-selective ion channel on giant liposomes. TMCO1 knockout mice reproduce the main clinical features of human cerebrofaciothoracic (CFT) dysplasia spectrum, a developmental disorder linked to TMCO1 dysfunction, and exhibit severe mishandling of ER Ca(2+) in cells. Our findings indicate that TMCO1 provides a protective mechanism to prevent overfilling of ER stores with Ca(2+) ions.