期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 283, 期 20, 页码 13842-13849出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M801510200
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资金
- NHLBI NIH HHS [R01 HL081092-01A2, R01 HL075165, R01 HL075165-03, R01 HL081092, P01 HL085098-01A10003, P01 HL085098] Funding Source: Medline
Mammalian target of rapamycin (mTOR) is a key regulator for cell growth through modulating components of the translation machinery. Previously, numerous pharmacological studies using rapamycin suggested that mTOR has an important role in regulating cardiac hypertrophic growth. To further investigate this assumption, we have generated two lines of cardiac specific mTOR transgenic mice, kinase-dead (kd) mTOR and constitutively active (ca) mTOR, using alpha-myosin heavy chain promoter. alpha-Myosin heavy chain (alpha MHC)-mTOR(kd) mice had a near complete inhibition of p70 S6k and 4E-BP1 phosphorylation, whereas alpha MHC-mTOR(ca) had a significant increase in p70 S6k and 4E-BP1 phosphorylation. Although the cardiac function of alpha MHC-mTOR(kd) mice was significantly altered, the cardiac morphology of these transgenic mice was normal. The cardiac hypertrophic growth in response to physiological and pathological stimuli was not different in alpha MHC-mTOR(kd) and alpha MHC-mTOR(ca) transgenic mice when compared with that of nontransgenic litter-mates. These findings suggest that the mTOR-mediated signaling pathway is not essential to cardiac hypertrophic growth but is involved in regulating cardiac function. Additional analysis of cardiac responses to fasting-refeeding or acute insulin administration indicated that alpha MHC-mTOR(kd) mice had a largely impaired physiological response to nutrient energy supply and insulin stimulation.
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