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[苯丙氨酸对小鼠成肌细胞系C2C12葡萄糖摄取的影响及其与mTOR-p70S6K信号通路的关系]

[Effects of Phenylalanine on Glucose Uptake in Mouse Myoblast Cell Line C2C12 and Its Relationship with mTOR-p70S6K Pathway].

作者信息

Du Rong, Du Juan, Tian Hao-Ming, Chen Tao, Gao Yun, Long Yang, Liu Dan

机构信息

Department of Endocrinology and Metabolism,West China Hospital,Sichuan University,Chengdu 610041,China.

The Affiliated Hospital of Southwest Mdicial University,Luzhou 646000,China.

出版信息

Sichuan Da Xue Xue Bao Yi Xue Ban. 2018 May;49(3):369-373.

PMID:30014636
Abstract

OBJECTIVE

To investigate the influence of phenylalanine(Phe) on glucose uptake in mouse myoblast cell line C2C12 and to explore its relationship with mTOR-p70S6K pathway.

METHODS

C2C12 cells were cultured to promote formation of multinucleated myotubes The cells were deprived and incubated with Phe at different concentrations (1.25,2.5,5,10,20 mmol/L).Krebs-Ringer buffer (KRB) was used as control.The 2-NBDG was used to measure glucose uptake of C2C12.The expression of mTOR,p70S6K,IRS-1,and Akt protein were evaluated by Western blot.

RESULTS

Compared with KBP treatment,glucose uptake of the cells incubated with 5 mmol/L leucine (Leu) was decreased by 30% (=0.001), while a 40% increase was detected in the cells incubated with 5 mmol/L Phe (<0.01).The promotion of glucose uptake was Phe concentration-dependent.Phe stimulation had no effect on the phosphorylation of mTOR at Ser2448. Phosphorylation of p70S6K at Thr389 was inhibited in the cells incubated with Phe at concentration higher than 1.25 mmol/L, but the difference was not significant (=0.815). Leu stimulated but Phe over 1.25 mmol/L inhibited phosphorylation of IRS-1 at Ser636/639, although the difference was not significant (=0.381).Neither Leu nor Phe affected the expression of phospho-Akt (Ser473) significantly.

CONCLUSION

Phenylalanine inhibits phosphorylation of IRS-1 at Ser636/639 possibly through inhibiting the activation of p70S6K.The effect of Phe on mTOR-p70S6K pathway is Akt-independent.

摘要

目的

研究苯丙氨酸(Phe)对小鼠成肌细胞系C2C12葡萄糖摄取的影响,并探讨其与mTOR-p70S6K信号通路的关系。

方法

培养C2C12细胞以促进多核肌管形成。将细胞饥饿处理后,用不同浓度(1.25、2.5、5、10、20 mmol/L)的Phe孵育。用Krebs-Ringer缓冲液(KRB)作为对照。用2-NBDG检测C2C12细胞的葡萄糖摄取。通过蛋白质免疫印迹法评估mTOR、p70S6K、IRS-1和Akt蛋白的表达。

结果

与KRB处理相比,5 mmol/L亮氨酸(Leu)孵育的细胞葡萄糖摄取降低了30%(P=0.001),而5 mmol/L Phe孵育的细胞葡萄糖摄取增加了40%(P<0.01)。Phe对葡萄糖摄取的促进作用呈浓度依赖性。Phe刺激对Ser2448位点的mTOR磷酸化无影响。浓度高于1.25 mmol/L的Phe孵育的细胞中,Thr389位点的p70S6K磷酸化受到抑制,但差异不显著(P=0.815)。Leu刺激而1.25 mmol/L以上的Phe抑制Ser636/639位点的IRS-1磷酸化,尽管差异不显著(P=0.381)。Leu和Phe均未显著影响磷酸化Akt(Ser473)的表达。

结论

苯丙氨酸可能通过抑制p70S6K的激活来抑制Ser636/639位点的IRS-1磷酸化。Phe对mTOR-p70S6K信号通路的作用不依赖于Akt。

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