Myocellular creatine and creatine transporter serine phosphorylation after starvation

被引:16
|
作者
Zhao, CR [1 ]
Shang, LH [1 ]
Wang, WY [1 ]
Jacobs, DO [1 ]
机构
[1] Creighton Univ, Sch Med, Dept Surg, Med Ctr,Surg Res Lab, Omaha, NE 68131 USA
关键词
creatine transporter; protein phosphorylation; guanidinoacetate methyltransferase; guanidinoacetic acid; creatine kinase; skeletal muscle membrane vesicle; creatine uptake; starvation; luminometry;
D O I
10.1006/jsre.2002.6431
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. Myocellular creatine, which is critically important for normal energy metabolism, increases in rat gastrocnemius muscle after starvation via unknown mechanisms. Creatine (Cr) uptake across plasma membranes is governed by a single, specific transporter (CrTr) that shares 50% amino acid sequence identity with GABA/choline/betaine transporters whose functions are modulated by phosphorylation. Methods. Gastrocnemius muscle was collected from adult male Sprague-Dawley (225-250 g) rats that were randomized to receive normal rat chow and distilled water ad libitum (CTL) or distilled water alone for 4 days (STV). Total Cr, phosphocreatine (PCr), free Cr, and ATP were measured luminometrically. CrTr protein expression and protein serine and tyrosine phosphorylation and mRNA expression were determined using immunoprecipitation and quantitative Western blotting and reverse transcription polymerase chain reaction (RT-PCR) analyses, respectively. Guanidinoacetate methyltransferase (GAMT) activity, guanidinoacetic acid (GAA) content, creatine kinase (CK) activity, and creatinine (Crn) content were assayed luminometrically or spectrophotometrically. Creatine transporter uptake activity was also measured in skeletal muscle membrane vesicles. Data were analyzed by t test. Results. Total Cr and free Cr increased 26 and 280% in STV (32.3 +/- 1.0 and 12.9 +/- 1.4 vs 25.7 +/- 1.1 and 3.4 +/- 0.9 mumol/g wet wt, mean +/- SEM, respectively, P < 0.01) hereas PCr content decreased 18% (18.6 +/- 0.8 vs 22.8 +/- 0.9 mumol/g wet wt, STV vs CTL P < 0.05). CrTr protein and mRNA expression, ATP, GAA, CK, GAMT, and protein tyrosine phosphorylation of CrTr were not significantly different between the two groups. However, protein serine phosphorylation of CrTr was significantly reduced by 30% (P < 0.05) anti creatine uptake activity was significantly increased (P < 0.05) in starved animals. Conclusion. Increases in myocellular creatine content after starvation are associated with reduced serine phosphorylation of the creatine transporter. (C) 2002 Elsevier Science (USA).
引用
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页码:10 / 16
页数:7
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