Frick G P, Lowenstein J M
J Biol Chem. 1978 Feb 25;253(4):1240-4.
Rat hearts were perfused simultaneously with [8-3H] AMP and [8-14C]adenosine. [8-3H] AMP was hydrolzyed by 5'-nucleotidase to produce intra- and extracellular [8-3H] adenosine. Comparison of the specific activities of [3H]- and [14C]adenosine in the heart cells with the specific activities of [3H]- and [14C]adenosine in the effluent perfusate showed that much more [3H]adenosine accumulated in the tissue than would be expected if extracellular adenosine were the immediate precursor of intracellular adenosine. Conversely, perfusion of rat hearts with [8-14C]AMP and [8-3H]adenosine led to a much greater accumulation of intracellular [14C]adenosine than would be expected from an uptake of adenosine from the perfusate. These results are interpreted to be due to hydrolysis of extracellular AMP by 5'-nucleotidase, located in the plasma membrane, and release of the resulting adenosine inside the cell. Measurements of the specific activities of 3H and 14C in ATP, ADP, AMP, and inosine support this interpretation.
用[8-³H] AMP和[8-¹⁴C]腺苷同时灌注大鼠心脏。[8-³H] AMP被5'-核苷酸酶水解,产生细胞内和细胞外的[8-³H]腺苷。将心脏细胞中[³H] -和[¹⁴C] -腺苷的比活性与流出灌流液中[³H] -和[¹⁴C] -腺苷的比活性进行比较,结果表明,如果细胞外腺苷是细胞内腺苷的直接前体,那么组织中积累的[³H]腺苷要比预期的多得多。相反,用[8-¹⁴C] AMP和[8-³H]腺苷灌注大鼠心脏,导致细胞内[¹⁴C]腺苷的积累比从灌流液中摄取腺苷所预期的要多得多。这些结果被解释为是由于位于质膜上的5'-核苷酸酶对细胞外AMP的水解,以及由此产生的腺苷在细胞内的释放。对ATP、ADP、AMP和肌苷中³H和¹⁴C比活性的测量支持了这一解释。