Talor Z, Emmanouel D S, Katz A I
J Clin Invest. 1982 May;69(5):1136-46. doi: 10.1172/jci110549.
Insulin influences certain metabolic and transport renal functions and is avidly degraded by the kidney, but the relative contribution of the luminal and basolateral tubular membranes to these events remains controversial. We studied (125)I-insulin degradation [TCA and immunoprecipitation (IP) methods] and the specific binding of the hormone by purified luminal (L) and basolateral (BL) tubular membranes. These were prepared from rabbit kidney cortical homogenates by differential and gradient centrifugation and ionic precipitation steps in sequence, which resulted in enrichment vs. homogenate of marker enzymes' activities (sodium-potassium-activated adenosine triphosphatase for BL and maltase for L) of 8- and 12-fold, respectively. Both fractions degraded insulin avidly and bound the hormone specifically without saturation even at pharmacologic concentrations (10 muM). At physiologic insulin concentrations (0.157 nM) BL membranes degraded substantial amounts of insulin (44.2+/-2.6 and 40.7+/-2.2 pg/mg protein per min by the TCA and IP methods, respectively), even though at lesser rates (P < 0.001) than the luminal fraction (67.2+/-2.3 and 75+/-6.2 pg/mg protein per min, respectively); the rate of insulin catabolism by BL membranes was significantly higher (P < 0.001) than that which could be attributed to their contamination by luminal components [12.2+/-1.9 pg/mg per min (TCA method), or 13.7+/-1.9 pg/mg per min (IP method)]. Competition experiments suggested that insulin-degrading activity in both fractions includes both specific and nonspecific components. In contrast to degradation, insulin binding by both membranes was highly specific for native insulin and was severalfold higher in BL than L membranes [17.5+/-1.3 vs. 4.5+/-0.4 fmol/mg protein (P < 0.001) at physiologic insulin concentrations]. Despite the marked difference in the binding capacity for insulin by the two membranes, the patterns of labeled insulin displacement by increasing amounts of unlabeled hormone were superimposable (50% displacement required approximately 3 nM), suggesting that their receptors' affinity for insulin was similar. These observations provide direct evidence that interaction of insulin with the kidney involves binding and degradation of the hormone at the peritubular cell membrane.
胰岛素影响肾脏的某些代谢和转运功能,且在肾脏中被大量降解,但肾小管腔面膜和基底侧膜在这些过程中的相对作用仍存在争议。我们研究了¹²⁵I胰岛素的降解(采用三氯乙酸和免疫沉淀法)以及纯化的肾小管腔面膜(L)和基底侧膜(BL)对该激素的特异性结合。这些膜是通过依次进行差速离心、梯度离心和离子沉淀步骤,从兔肾皮质匀浆中制备得到的,结果显示标记酶活性(基底侧膜的钠钾激活三磷酸腺苷酶和腔面膜的麦芽糖酶)相对于匀浆分别富集了8倍和12倍。两个组分都能快速降解胰岛素,并特异性结合该激素,即使在药理浓度(10 μM)下也不会饱和。在生理胰岛素浓度(0.157 nM)下,基底侧膜能降解大量胰岛素(通过三氯乙酸法和免疫沉淀法分别为44.2±2.6和40.7±2.2 pg/mg蛋白质每分钟),尽管降解速率(P<0.001)低于腔面膜组分(分别为67.2±2.3和75±6.2 pg/mg蛋白质每分钟);基底侧膜的胰岛素分解代谢速率显著高于(P<0.001)因腔面膜成分污染而导致的分解代谢速率[12.2±1.9 pg/mg每分钟(三氯乙酸法)或13.7±1.9 pg/mg每分钟(免疫沉淀法)]。竞争实验表明,两个组分中的胰岛素降解活性包括特异性和非特异性成分。与降解情况不同,两种膜对胰岛素的结合对天然胰岛素具有高度特异性,且在生理胰岛素浓度下,基底侧膜的结合量比腔面膜高几倍[分别为17.5±1.3和4.5±0.4 fmol/mg蛋白质(P<0.001)]。尽管两种膜对胰岛素的结合能力存在显著差异,但随着未标记激素量增加,标记胰岛素的置换模式是可叠加的(50%置换所需浓度约为3 nM),这表明它们的受体对胰岛素的亲和力相似。这些观察结果提供了直接证据,表明胰岛素与肾脏的相互作用涉及该激素在肾小管周围细胞膜上的结合和降解。