Mammalian target of rapamycin: A metabolic rheostat for regulating adipose tissue function and cardiovascular ealth Review


Authors: Wipperman, M. F.; Montrose, D. C.; Gotto, A. M. Jr; Hajjar, D. P.
Review Title: Mammalian target of rapamycin: A metabolic rheostat for regulating adipose tissue function and cardiovascular ealth
Abstract: The complex relationship between diet and metabolism is an important contributor to cellular metabolism and health. Over the past few decades, a central role for mammalian target of rapamycin (mTOR) in the regulation of multiple cellular processes, including the response to food intake, maintaining homeostasis, and the pathogenesis of disease, has been shown. Herein, we first review our current understanding of the biochemical functions of mTOR and its response to fluctuations in hormone levels, like insulin. Second, we highlight the role of mTOR in lipogenesis, adipogenesis, β-oxidation of lipids, and ketosis of carbohydrates, lipids, and proteins. Special attention is paid to recent advances in mTOR signaling in white versus brown adipose tissues. Finally, we review how mTOR regulates cardiovascular health and disease. Together, these insights define a clearer picture of the connection between mTOR signaling, metabolic health, and disease. © 2019 American Society for Investigative Pathology
Keywords: review; nonhuman; protein function; metabolism; protein protein interaction; lipid; cardiovascular disease; mammalian target of rapamycin; insulin; amino acid; glucose; adenosine triphosphate; biochemistry; mtor signaling; lipogenesis; carbohydrate; adipose tissue; metabolic regulation; glucose metabolism; brown adipose tissue; white adipose tissue; mammalian target of rapamycin complex 1; adipogenesis; energy yield; amino acid metabolism; rheb protein; ketoacidosis; lipid oxidation; human; priority journal; cardiovascular function
Journal Title: American Journal of Pathology
Volume: 189
Issue: 3
ISSN: 0002-9440
Publisher: Elsevier Science, Inc.  
Date Published: 2019-03-01
Start Page: 492
End Page: 501
Language: English
DOI: 10.1016/j.ajpath.2018.11.013
PUBMED: 30803496
PROVIDER: scopus
PMCID: PMC6412382
DOI/URL:
Notes: Source: Scopus
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