Investigating the Causes for Decreased Levels of Glutathione in Individuals with Type II Diabetes

被引:77
作者
Lagman, Minette [1 ,2 ]
Ly, Judy [2 ]
Saing, Tommy [1 ]
Singh, Manpreet Kaur [1 ,2 ]
Tudela, Enrique Vera [1 ,2 ]
Morris, Devin [2 ]
Chi, Po-Ting [1 ,2 ]
Ochoa, Cesar [3 ]
Sathananthan, Airani [3 ]
Venketaraman, Vishwanath [1 ,2 ]
机构
[1] Western Univ Hlth Sci, Grad Coll Biomed Sci, Pomona, CA 91766 USA
[2] Western Univ Hlth Sci, Coll Osteopath Med Pacific, Dept Basic Med Sci, Pomona, CA USA
[3] Western Diabet Inst, Pomona, CA USA
关键词
MYCOBACTERIUM-TUBERCULOSIS; OXIDATIVE STRESS; RESISTANCE; INFECTION; RESPONSES; INNATE; CELLS; SUPPRESSION; CYTOKINES; IMMUNITY;
D O I
10.1371/journal.pone.0118436
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Tuberculosis (TB) remains an eminent global burden with one third of the world's population latently infected with Mycobacterium tuberculosis (M. tb). Individuals with compromised immune systems are especially vulnerable to M. tb infection. In fact, individuals with Type 2 Diabetes Mellitus (T2DM) are two to three times more susceptible to TB than those without T2DM. In this study, we report that individuals with T2DM have lower levels of glutathione (GSH) due to compromised levels of GSH synthesis and metabolism enzymes. Transforming growth factor beta (TGF-beta), a cytokine that is known to decrease the expression of the catalytic subunit of glutamine-cysteine ligase (GCLC) was found in increased levels in the plasma samples from individuals with T2DM, explaining the possible underlying mechanism that is responsible for decreased levels of GSH in individuals with T2DM. Moreover, increased levels of pro-inflammatory cytokines such as interleukin-6 (IL-6) and interleukin-17 (IL-17) were observed in plasma samples isolated from individuals with T2DM. Increased levels of IL-6 and IL-17 was accompanied by enhanced production of free radicals further indicating an alternative mechanism for the decreased levels of GSH in individuals with T2DM. Augmenting the levels of GSH in macrophages isolated from individuals with T2DM resulted in improved control of M. tb infection. Furthermore, cytokines that are responsible for controlling M. tb infection at the cellular and granuloma level such as tumor necrosis factor alpha (TNF-alpha), interleukin-1 beta (IL-1 beta), interleukin-2 (IL-2), interferon-gamma (IFN-gamma), and interleukin-12 (IL-12), were found to be compromised in plasma samples isolated from individuals with T2DM. On the other hand, interleukin-10 (IL-10), an immunosuppressive cytokine was increased in plasma samples isolated from individuals with T2DM. Overall, these findings suggest that lower levels of GSH in individuals with T2DM lead to their increased susceptibility to M. tb infection.
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页数:19
相关论文
共 38 条
[1]   Glutathione-Redox Balance Regulates c-rel-Driven IL-12 Production in Macrophages: Possible Implications in Antituberculosis Immunotherapy [J].
Alam, Kaiser ;
Ghousunnissa, Sheikh ;
Nair, Shiny ;
Valluri, Vijaya Lakshmi ;
Mukhopadhyay, Sangita .
JOURNAL OF IMMUNOLOGY, 2010, 184 (06) :2918-2929
[2]  
Alkozai Edris M, 2014, F1000Res, V3, P85, DOI 10.12688/f1000research.3316.1
[3]  
American Diabetes Association, 2013, DAT STAT DIAB
[4]  
[Anonymous], 2014, TUB
[5]  
[Anonymous], 2014, National Diabetes Statistics Report
[6]  
[Anonymous], 2011, USE GLYCATED HAEMOGL
[7]   Smad3-ATF3 signaling mediates TGF-β suppression of genes encoding Phase II detoxifying proteins [J].
Bakin, AV ;
Stourman, NV ;
Sekhar, KR ;
Rinehart, C ;
Yan, XX ;
Meredith, MJ ;
Arteaga, CL ;
Freeman, ML .
FREE RADICAL BIOLOGY AND MEDICINE, 2005, 38 (03) :375-387
[8]   Contribution of polyol pathway to diabetes-induced oxidative stress [J].
Chung, SSM ;
Ho, ECM ;
Lam, KSL ;
Chung, SK .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 :S233-S236
[9]   Multi-Scale Modeling Predicts a Balance of Tumor Necrosis Factor-α and Interleukin-10 Controls the Granuloma Environment during Mycobacterium tuberculosis Infection [J].
Cilfone, Nicholas A. ;
Perry, Cory R. ;
Kirschner, Denise E. ;
Linderman, Jennifer J. .
PLOS ONE, 2013, 8 (07)
[10]  
COUSENS LP, 1995, J IMMUNOL, V155, P5690