Bird G S, Rossier M F, Obie J F, Putney J W
Laboratory of Cellular and Molecular Pharmacology, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709.
J Biol Chem. 1993 Apr 25;268(12):8425-8.
Stimulation of mouse lacrimal acinar cells with submaximal concentrations of the muscarinic agonist, methacholine, resulted in an increase in intracellular calcium ([Ca2+]i), which took the form of sinusoidal oscillations. These oscillations were relatively constant (approximately 4-5/min) regardless of the methacholine concentration, suggesting that the oscillations arise from an oscillating negative feedback in the signal transduction pathway. This negative feedback appears to involve oscillations in protein kinase C activity because the oscillations were prevented by activation, inhibition, or down-regulation of protein C. Activation of protein kinase C with phorbol esters inhibited the methacholine-induced [Ca2+]i signal and formation of the Ca2+ mobilizing messenger, inositol 1,4,5-trisphosphate. [Ca2+]i signals elicited by intracellular introduction of inositol phosphates did not oscillate and were not affected by activators or inhibitors of protein kinase C. Thus, the constant frequency [Ca2+]i oscillations appear to result from a negative feedback loop involving inhibition of inositol trisphosphate production by protein kinase C.
用亚最大浓度的毒蕈碱激动剂乙酰甲胆碱刺激小鼠泪腺腺泡细胞,导致细胞内钙([Ca2+]i)增加,其形式为正弦振荡。无论乙酰甲胆碱浓度如何,这些振荡相对恒定(约4-5次/分钟),这表明振荡源于信号转导途径中的振荡负反馈。这种负反馈似乎涉及蛋白激酶C活性的振荡,因为通过蛋白C的激活、抑制或下调可阻止振荡。佛波酯激活蛋白激酶C可抑制乙酰甲胆碱诱导的[Ca2+]i信号以及钙动员信使肌醇1,4,5-三磷酸的形成。细胞内引入肌醇磷酸引发的[Ca2+]i信号不发生振荡,且不受蛋白激酶C激活剂或抑制剂的影响。因此,恒定频率的[Ca2+]i振荡似乎源于涉及蛋白激酶C抑制肌醇三磷酸产生的负反馈回路。