Ceramide-activated protein kinases A an C zeta inhibit kidney proximal tubule cell Na+-ATPase

被引:16
作者
Cabral, Lindsey M. P.
Wengert, Mira
Almeida, Fernando G.
Caruso-Neves, Celso
Vieyra, Adalberto
Einicker-Lamas, Marcelo [1 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Biofis Carlos Chagas Filho, BR-21941902 Rio De Janeiro, Brazil
关键词
Bioactive sphingolipids; Renal plasma membrane; Atypical PKC isoform; Na+ transport; Renal ATPases; BASOLATERAL MEMBRANES; ANGIOTENSIN-II; ADENOSINE-TRIPHOSPHATASE; MOLECULAR-CLONING; SODIUM-PUMP; PATHWAY; RECEPTOR; CORTEX; SPHINGOMYELINASE; SPHINGOLIPIDS;
D O I
10.1016/j.abb.2010.04.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The basolateral membranes of kidney proximal tubule cells have (Na+-K+)-ATPase and Na+-ATPase activities, involved in Na+ reabsorption. We showed that ceramide (Cer) modulates protein kinase A (PKA) and protein kinase C (PKC), which are involved in regulating ion transporters. Here we show that ceramide, promotes 60% inhibition of Na+-ATPase activity (I-50 approximate to 100 nM). This effect was completely reversed by inhibiting PKA but did not involve the classic PKC signaling pathway. In these membranes we found the Cer-activated atypical PKC zeta (PKC zeta) isoform. When PKC zeta is inhibited, Cer ceases to inhibit the Na+-ATPase, allowing the cAMP/PKA signaling pathway to recover its stimulatory effect on the pump. There were no effects on the (Ne+K+)-ATPase. These results reveal Cer as a potent physiological modulator of the Na+-ATPase, participating in a regulatory network in kidney cells and counteracting the stimulatory effect of PKA via PKC zeta. (c) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:57 / 61
页数:5
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