Molitoris B A, Alfrey A C, Harris R A, Simon F R
Am J Physiol. 1985 Jul;249(1 Pt 2):F12-9. doi: 10.1152/ajprenal.1985.249.1.F12.
Renal proximal tubule cells adapt to dietary phosphate (Pi) restriction by increasing Pi transport independent of parathyroid hormone, vitamin D metabolites, or serum Ca2+. To determine the underlying cellular mechanism(s), brush border (BBM) and basolateral membranes (BLM) were isolated from growing male rats fed a synthetic diet containing variable levels of Pi (0.1-1.4%). Dietary Pi restriction was without effect on either BBM or BLM total lipid phosphorus, individual phospholipid species, or BLM Na+-K+-ATPase specific activity. However, dietary Pi restriction (0.1 vs. 1.0%) did cause a significant reduction in BBM but not BLM cholesterol (0.45 vs. 0.41 mumol/mg protein). Brush border membrane cholesterol was inversely correlated with the tubular reabsorption of Pi (r = 0.77, P less than 0.01) over a broad range (99.9-46.2%). Arrhenius analysis of two intrinsic BBM enzymes revealed a significant reduction in the breakpoint temperature for alkaline phosphatase but no change for Mg2+-ATPase. Fluorescence polarization studies showed increased BBM inner core fluidity due to an alteration in neutral lipids but not phospholipid, fatty acid, or protein membrane components. These data demonstrate that the BBM can regulate its cholesterol content independent of the BLM. Furthermore, they suggest that adaptation to dietary Pi restriction involves a reduction in BBM cholesterol, which may be mediated by an increase in membrane fluidity.
肾近端小管细胞通过增加磷转运来适应饮食中磷(Pi)的限制,这种增加与甲状旁腺激素、维生素D代谢物或血清Ca2+无关。为了确定潜在的细胞机制,从喂食含不同磷水平(0.1 - 1.4%)合成饮食的生长雄性大鼠中分离出刷状缘(BBM)和基底外侧膜(BLM)。饮食中磷的限制对BBM或BLM的总脂质磷、单个磷脂种类或BLM的Na+-K+-ATP酶比活性均无影响。然而,饮食中磷的限制(0.1%对1.0%)确实导致BBM胆固醇显著降低,但BLM胆固醇未降低(0.45对0.41 μmol/mg蛋白)。在很宽的范围内(99.9 - 46.2%),刷状缘膜胆固醇与磷的肾小管重吸收呈负相关(r = 0.77,P < 0.01)。对两种内在BBM酶的阿累尼乌斯分析显示,碱性磷酸酶的断点温度显著降低,但Mg2+-ATP酶无变化。荧光偏振研究表明BBM内核流动性增加,这是由于中性脂质而非磷脂、脂肪酸或蛋白质膜成分的改变所致。这些数据表明BBM可以独立于BLM调节其胆固醇含量。此外,它们提示对饮食中磷限制的适应涉及BBM胆固醇的降低,这可能由膜流动性增加介导。