Thiol dependent NF-κB suppression and inhibition of T-cell mediated adaptive immune responses by a naturally occurring steroidal lactone Withaferin A

被引:44
作者
Gambhir, Lokesh [1 ]
Checker, Rahul [1 ]
Sharma, Deepak [1 ]
Thoh, M. [1 ]
Patil, Anand [2 ]
Degani, M. [3 ]
Gota, Vikram [2 ]
Sandur, Santosh K. [1 ]
机构
[1] Bhabha Atom Res Ctr, Radiat Biol & Hlth Sci Div, Biosci Grp, Bombay 400085, Maharashtra, India
[2] Adv Ctr Treatment Res & Educ Canc, Kharghar, Navi Mumbai, India
[3] Inst Chem Technol, Bombay, Maharashtra, India
关键词
Anti-inflammatory; Cytokines; ROS; Graft-versus-host disease; Pharmacokinetics; ALPHA KINASE ACTIVATION; BREAST-CANCER CELLS; DOWN-REGULATION; COVALENT MODIFICATION; TRANSCRIPTION FACTORS; WITHANIA-SOMNIFERA; MEDICINAL-PLANTS; GENE-PRODUCTS; TUMOR-CELLS; DNA-BINDING;
D O I
10.1016/j.taap.2015.09.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Withaferin A (WA), a steroidal lactone isolated from ayurvedic medicinal plant Withania somnifera, was shown to inhibit tumor growth by inducing oxidative stress and suppressing NF-kappa B pathway. However, its effect on T-cell mediated adaptive immune responses and the underlying mechanism has not been investigated. Since both T-cell responses and NF-kappa B pathway are known to be redox sensitive, the present study was undertaken to elucidate the effect of WA on adaptive immune responses in vitro and in vivo. WA inhibited mitogen induced T-cell and B-cell proliferation in vitro without inducing any cell death. It inhibited upregulation of T-cell (CD25, CD69, CD71 and CD54) and B-cell (CD80, CD86 and MHC-II) activation markers and secretion of Th1 and Th2 cytokines. WA induced oxidative stress by increasing the basal ROS levels and the immunosuppressive effects of WA were abrogated only by thiol anti-oxidants. The redox modulatory effects of WA in T-cells were attributed to its ability to directly interact with free thiols. WA inhibited NF-kappa B nuclear translocation in lymphocytes and prevented the direct binding of nuclear NF-kappa B to its consensus sequence. MALDI-TOF analysis using a synthetic NF-kappa B-p50 peptide containing Cys-62 residue suggested that WA can modify the cysteine residue of NF-kappa B. The pharmacokinetic studies for WA were also carried out and in vivo efficacy of WA was studied using mouse model of Graft-versus-host disease. In conclusion, WA is a potent inhibitor of T-cell responses and acts via a novel thiol dependent mechanism and inhibition of NF-kappa B pathway. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:297 / 312
页数:16
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