Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/85649
Title: mTORC2/Akt activation in adipocytes is required for adipose tissue inflammation in tuberculosis
Authors: Martinez, Nuria
Cheng, Catherine Y.
Ketheesan, Natkunam
Cullen, Aidan
Tang, Yuefeng
Lum, Josephine
West, Kim
Poidinger, Michael
Guertin, David A.
Singhal, Amit
Kornfeld, Hardy
Keywords: Tuberculosis
Adipose Tissue
Science::Medicine
Issue Date: 2019
Source: Martinez, N., Cheng, C. Y., Ketheesan, N., Cullen, A., Tang, Y., Lum, J., . . . Kornfeld, H. (2019). mTORC2/Akt activation in adipocytes is required for adipose tissue inflammation in tuberculosis. EBioMedicine, 45, 314-327. doi:10.1016/j.ebiom.2019.06.052
Series/Report no.: EBioMedicine
Abstract: Background: Mycobacterium tuberculosis has co-evolved with the human host, adapting to exploit the immune system for persistence and transmission. While immunity to tuberculosis (TB) has been intensively studied in the lung and lymphoid system, little is known about the participation of adipose tissues and non-immune cells in the host-pathogen interaction during this systemic disease. Methods: C57BL/6J mice were aerosol infected with M. tuberculosis Erdman and presence of the bacteria and the fitness of the white and brown adipose tissues, liver and skeletal muscle were studied compared to uninfected mice. Findings: M. tuberculosis infection in mice stimulated immune cell infiltration in visceral, and brown adipose tissue. Despite the absence of detectable bacterial dissemination to fat tissues, adipocytes produced localized pro-inflammatory signals that disrupted adipocyte lipid metabolism, resulting in adipocyte hypertrophy. Paradoxically, this resulted in increased insulin sensitivity and systemic glucose tolerance. Adipose tissue inflammation and enhanced glucose tolerance also developed in obese mice after aerosol M. tuberculosis infection. We found that infection induced adipose tissue Akt signaling, while inhibition of the Akt activator mTORC2 in adipocytes reversed TB-associated adipose tissue inflammation and cell hypertrophy. Interpretation:Our study reveals a systemic response to aerosol M. tuberculosis infection that regulates adipose tissue lipid homeostasis through mTORC2/Akt signaling in adipocytes. Adipose tissue inflammation in TB is not simply a passive infiltration with leukocytes but requires the mechanistic participation of adipocyte signals.
URI: https://hdl.handle.net/10356/85649
http://hdl.handle.net/10220/49820
DOI: 10.1016/j.ebiom.2019.06.052
Rights: © 2019 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:LKCMedicine Journal Articles

Files in This Item:
File Description SizeFormat 
mTORC2Akt activation in adipocytes is required for adipose tissue.pdf4.43 MBAdobe PDFThumbnail
View/Open

Google ScholarTM

Check

Altmetric


Plumx

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.