Korman L Y, Lemp G F, Jackson M J, Gardner J D
Biochim Biophys Acta. 1982 Sep 13;721(1):47-54. doi: 10.1016/0167-4889(82)90022-2.
ATP, ADP and AMP but not adenosine increased cyclic AMP in dispersed enterocytes prepared from guinea pig small intestine. This action of ATP was augmented by IBMX and was reproduced by App(NH)p or App(CH2)p. ATP also increased the formation of cyclic [14C]AMP in enterocytes that had been preincubated with [14C]adenine. Gpp(NH)p and NaF each caused persistent activation of adenylate cyclase in plasma membranes from enterocytes and ATP caused significant augmentation of this persistent activation. In addition to increasing cellular cyclic AMP and augmenting Gpp(NH)p and NaF-stimulated persistent activation of adenylate cyclase, ATP increased the Isc across mounted strips of small intestine and inhibited net absorption of fluid and electrolytes in segments of everted small intestine. These results indicate that intestinal epithelial cells possess a receptor that interacts with ATP and other adenine nucleotides and that receptor occupation by ATP causes activation of adenylate cyclase, increased cyclic AMP and changes in active ion transport across intestinal mucosa.
ATP、ADP和AMP而非腺苷可增加从豚鼠小肠制备的分散肠上皮细胞中的环磷酸腺苷(cAMP)。IBMX增强了ATP的这一作用,且App(NH)p或App(CH2)p也可重现此作用。ATP还增加了预先用[14C]腺嘌呤预孵育的肠上皮细胞中环[14C]AMP的形成。Gpp(NH)p和NaF均可使肠上皮细胞质膜中的腺苷酸环化酶持续激活,而ATP可显著增强这种持续激活。除了增加细胞内cAMP以及增强Gpp(NH)p和NaF刺激的腺苷酸环化酶持续激活外,ATP还增加了横跨小肠固定条带的短路电流(Isc),并抑制外翻小肠段中液体和电解质的净吸收。这些结果表明,肠上皮细胞具有一种与ATP和其他腺嘌呤核苷酸相互作用的受体,ATP占据该受体可导致腺苷酸环化酶激活、cAMP增加以及肠道黏膜主动离子转运的变化。