Giovannelli A, Grassi F, Eusebi F, Miledi R
Dipartimento di Medicina Sperimentale Università dell'Aquila, Rome, Italy.
Proc Natl Acad Sci U S A. 1991 Mar 1;88(5):1808-11. doi: 10.1073/pnas.88.5.1808.
Whole-cell currents activated by acetylcholine (AcCho) were recorded in C2 mouse myotubes before and after prolonged treatment with tunicamycin, an inhibitor of glycosylation. In control cells the AcCho-induced currents decayed slowly even in the continuous presence of AcCho. After 24 hr of treatment with tunicamycin AcCho still elicited currents, but their size was significantly reduced and their decay was greatly accelerated. The binding of 125I-labeled alpha-bungarotoxin, a specific and irreversible antagonist of muscle AcCho receptors, was greatly reduced after tunicamycin treatment, and an equivalent reduction was observed after a long-lasting application of the AcCho agonist carbachol. We suggest that, after inhibition of glycosylation by tunicamycin, AcCho receptors are expressed correctly on the plasma membrane but these receptors desensitize more rapidly and are less efficient in binding alpha-bungarotoxin.
在用糖基化抑制剂衣霉素进行长时间处理前后,记录了C2小鼠肌管中由乙酰胆碱(AcCho)激活的全细胞电流。在对照细胞中,即使在持续存在乙酰胆碱的情况下,乙酰胆碱诱导的电流也缓慢衰减。在用衣霉素处理24小时后,乙酰胆碱仍能引发电流,但其大小显著减小,衰减大大加速。125I标记的α-银环蛇毒素(一种肌肉乙酰胆碱受体的特异性不可逆拮抗剂)的结合在衣霉素处理后大大减少,在长期应用乙酰胆碱激动剂卡巴胆碱后也观察到了同等程度的减少。我们认为,在衣霉素抑制糖基化后,乙酰胆碱受体在质膜上正确表达,但这些受体脱敏更快,且结合α-银环蛇毒素的效率更低。