4.7 Review

The central moTOR of metabolism

期刊

DEVELOPMENTAL CELL
卷 57, 期 6, 页码 691-706

出版社

CELL PRESS
DOI: 10.1016/j.devcel.2022.02.024

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资金

  1. NIH BIRCWH [K12HD101368]
  2. University of Wisconsin-Madison School Department of Biochemistry
  3. Diabetes Research Center at Washington University in St. Louis of the National Institutes of Health [P30DK020579]
  4. NIH/NIA [AG056771, AG062328, AG061635]
  5. NIH/NIDDK [DK125859]
  6. U.S. Department of Veterans Affairs [I01-BX004031]
  7. University of Wisconsin-Madison School of Medicine and Public Health and Department of Medicine
  8. William S. Middleton Memorial Veterans Hospital

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This review discusses the importance of protein kinase mechanistic target of rapamycin (mTOR) in metabolic regulation, its role in regulating the metabolism of the four macromolecular building blocks of the cell, and its impact on organismal physiology and aging. It also explores the potential clinical application of mTOR inhibitors in the treatment and prevention of age-related diseases.
The protein kinase mechanistic target of rapamycin (mTOR) functions as a central regulator of metabolism, integrating diverse nutritional and hormonal cues to control anabolic processes, organismal physiology, and even aging. This review discusses the current state of knowledge regarding the regulation of mTOR signaling and the metabolic regulation of the four macromolecular building blocks of the cell: carbohydrate, nucleic acid, lipid, and protein by mTOR. We review the role of mTOR in the control of organismal physiology and aging through its action in key tissues and discuss the potential for clinical translation of mTOR inhibition for the treatment and prevention of diseases of aging.

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