Janecki A J, Janecki M, Akhter S, Donowitz M
Department of Medicine, Division of Gastroenterology, Hepatology, and Nutrition, University of Texas Medical School, Houston, Texas 77030, USA.
J Biol Chem. 2000 Mar 17;275(11):8133-42. doi: 10.1074/jbc.275.11.8133.
Na(+)/H(+) exchanger NHE3 is a plasma membrane (PM) protein, which contributes to Na(+) absorption in the intestine. Growth factors stimulate NHE3 via phosphatidylinositol 3-kinase (PI3-K), but mechanism of this process is not clear. To examine the hypothesis that growth factors stimulate NHE3 by modulating NHE3 recycling, and that PI3-K participates in this mechanism, we used PS120 fibroblasts expressing a fusion protein of NHE3 and green fluorescent protein. At steady state, approximately 25% of cellular NHE3 content was expressed at PM. Inhibition of PI3-K decreased PM expression of NHE3, which correlated with retention of the exchanger in recycling endosomal compartment. In contrast, basic fibroblast growth factor (bFGF) increased PM expression of NHE3, which was associated with a 2-fold increase in rate constant for exit of the exchanger from the recycling compartment. Qualitatively similar effects of bFGF were observed in cells pretreated with PI3-K inhibitors, but their magnitude was only approximately 50% of that in intact cells. These data suggest that: (i) bFGF stimulates NHE3 by increasing PM expression of the exchanger; (ii) PI3-K mediates PM expression of NHE3 in both basal and bFGF-stimulated conditions, and (iii) not all of the effects of bFGF on NHE3 expression are mediated by PI3-K, suggesting additional regulatory mechanisms.
钠/氢交换体NHE3是一种质膜(PM)蛋白,它有助于肠道中的钠吸收。生长因子通过磷脂酰肌醇3激酶(PI3-K)刺激NHE3,但这一过程的机制尚不清楚。为了检验生长因子通过调节NHE3循环来刺激NHE3以及PI3-K参与这一机制的假说,我们使用了表达NHE3与绿色荧光蛋白融合蛋白的PS120成纤维细胞。在稳态下,约25%的细胞NHE3含量在质膜上表达。抑制PI3-K会降低NHE3在质膜上的表达,这与该交换体保留在循环内体区室有关。相反,碱性成纤维细胞生长因子(bFGF)增加了NHE3在质膜上的表达,这与该交换体从循环区室排出的速率常数增加2倍相关。在用PI3-K抑制剂预处理的细胞中观察到bFGF有定性相似的作用,但其程度仅约为完整细胞中的50%。这些数据表明:(i)bFGF通过增加该交换体在质膜上的表达来刺激NHE3;(ii)PI3-K在基础和bFGF刺激条件下均介导NHE3在质膜上的表达;(iii)bFGF对NHE3表达的所有作用并非都由PI3-K介导,提示存在其他调节机制。