Premium
Modulation of TSC–mTOR Signaling on Immune Cells in Immunity and Autoimmunity
Author(s) -
Yang Hui,
Wang Xianghui,
Zhang Yan,
Liu Huanrong,
Liao Jiongbo,
Shao Kun,
Chu Yiwei,
Liu Guangwei
Publication year - 2014
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.24426
Subject(s) - pi3k/akt/mtor pathway , tsc1 , immune system , microbiology and biotechnology , rptor , biology , mechanistic target of rapamycin , autoimmunity , acquired immune system , mtorc2 , regulator , signal transduction , t cell , mtorc1 , immunology , genetics , gene
The mammalian target of rapamycin (mTOR) is an evolutionarily conserved serine/threonine kinase which has a central role in the regulation of cell growth and metabolism. In the study of the mTOR signaling pathway, tuberous sclerosis complex (TSC) 1/2 complex is identified as a critical regulator of mTOR activity. TSC1/2 plays important roles for immune cell homeostasis and differentiation by negative control of mTOR signaling pathway. TSC1/2–mTOR pathway is proving to be a central point in regulating immune function of diverse immune cells. In this review, we discuss the function of TSC1/2–mTOR to direct the innate and adaptive immune cell development and function. Furthermore, we focus on the role of TSC1/2–mTOR signaling pathway in immune cell mediated diseases, especially autoimmunity. J. Cell. Physiol. 229: 17–26, 2014. © 2013 Wiley Periodicals, Inc.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom