大豆凝集素触发的IL-6分泌通过P2RX7依赖性激活JAK2/STAT3/Mcl-1途径诱导自噬杀死细胞内分枝杆菌。

IF 3.7 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Abtar Mishra , Ashish Kumar , Lincoln Naik , Salina Patel , Mousumi Das , Assirbad Behura , Dev Kiran Nayak , Amit Mishra , Sujit K. Bhutia , Ramandeep Singh , Rohan Dhiman
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引用次数: 0

摘要

细胞因子治疗和细胞因子介导的自噬已被用作抑制结核分枝杆菌在宿主细胞中生长的主要宿主导向治疗(HDT)方法。在本研究中,我们通过细胞因子介导的自噬诱导分化的THP-1(dTHP-1)细胞,分析了大豆凝集素(SBL)的抗结核活性。SBL处理后,在未感染和分枝杆菌感染的dTHP-1细胞中通过P2RX7介导的PI3K/Akt/CREB依赖性信号传导途径观察到IL-6表达显著增加。使用IL-6中和抗体或相关信号抑制IL-6水平显著增强SBL处理的dTHP-1细胞中的分枝杆菌载量。此外,IL-6通过其受体诱导的Mcl-1表达的自分泌信号通过JAK2/STAT3途径激活自噬,并且该途径的抑制影响自噬。最后,通过NSC 33994(一种JAK2抑制剂)或S63845(一种Mcl-1抑制剂)阻断IL-6调节的自噬,导致SBL处理的细胞内分枝杆菌生长显著增加。总之,这些结果表明SBL与P2RX7相互作用以调节PI3K/Akt/CREB网络,从而在dTHP-1细胞中释放IL-6。释放的IL-6反过来在与IL-6Rα相互作用时激活JAK2/STAT3/Mcl-1通路,以调节自噬,最终控制巨噬细胞中分枝杆菌的生长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Soybean lectin-triggered IL-6 secretion induces autophagy to kill intracellular mycobacteria through P2RX7 dependent activation of the JAK2/STAT3/Mcl-1 pathway

Soybean lectin-triggered IL-6 secretion induces autophagy to kill intracellular mycobacteria through P2RX7 dependent activation of the JAK2/STAT3/Mcl-1 pathway

Cytokine therapy and cytokine-mediated autophagy have been used as prominent host-directed therapy (HDT) approaches to restrain M. tb growth in the host cell. In the present study, we have dissected the anti-tubercular activity of Soybean lectin (SBL) through cytokine-mediated autophagy induction in differentiated THP-1 (dTHP-1) cells. A significant increase in IL-6 expression was observed in both uninfected and mycobacteria infected dTHP-1 cells through the P2RX7 mediated pathway via PI3K/Akt/CREB-dependent signalling after SBL treatment. Inhibition of IL-6 level using IL-6 neutralizing antibody or associated signalling significantly enhanced the mycobacterial load in SBL-treated dTHP-1 cells. Further, autocrine signalling of IL-6 through its receptor-induced Mcl-1 expression activated autophagy via JAK2/STAT3 pathway, and inhibition of this pathway affected autophagy. Finally, blocking the IL-6-regulated autophagy through NSC 33994 (a JAK2 inhibitor) or S63845 (an Mcl-1 inhibitor) led to a notable increase in intracellular mycobacterial growth in SBL-treated cells. Taken together, these results indicate that SBL interacts with P2RX7 to regulate PI3K/Akt/CREB network to release IL-6 in dTHP-1 cells. The released IL-6, in turn, activates the JAK2/STAT3/Mcl-1 pathway upon interaction with IL-6Rα to modulate autophagy that ultimately controls mycobacterial growth in macrophages.

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来源期刊
Cytokine
Cytokine 医学-免疫学
CiteScore
7.60
自引率
2.60%
发文量
262
审稿时长
48 days
期刊介绍: The journal Cytokine has an open access mirror journal Cytokine: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. * Devoted exclusively to the study of the molecular biology, genetics, biochemistry, immunology, genome-wide association studies, pathobiology, diagnostic and clinical applications of all known interleukins, hematopoietic factors, growth factors, cytotoxins, interferons, new cytokines, and chemokines, Cytokine provides comprehensive coverage of cytokines and their mechanisms of actions, 12 times a year by publishing original high quality refereed scientific papers from prominent investigators in both the academic and industrial sectors. We will publish 3 major types of manuscripts: 1) Original manuscripts describing research results. 2) Basic and clinical reviews describing cytokine actions and regulation. 3) Short commentaries/perspectives on recently published aspects of cytokines, pathogenesis and clinical results.
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