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对JAK/STAT3信号通路的靶向阻断可抑制肝星状细胞的增殖、迁移和胶原蛋白生成,并诱导其凋亡。

Targeted blockade of JAK/STAT3 signaling inhibits proliferation, migration and collagen production as well as inducing the apoptosis of hepatic stellate cells.

作者信息

Gu Yuan-Jing, Sun Wu-Yi, Zhang Sen, Li Xin-Ran, Wei Wei

机构信息

Institute of Clinical Pharmacology, Anhui Medical University, Key Laboratory of Anti-inflammatory and Immune Medicine, Ministry of Education, Anhui Collaborative Innovation Center of Anti-inflammatory and Immune Medicine, Hefei, Anhui 230032, P.R. China.

出版信息

Int J Mol Med. 2016 Sep;38(3):903-11. doi: 10.3892/ijmm.2016.2692. Epub 2016 Jul 26.

Abstract

Protein tyrosine kinases belonging to the Janus kinase (JAK) family are associated with many cytokine receptors, which, on ligand binding, regulate important cellular functions such as proliferation, apoptosis and differentiation. The protective effects of JAK inhibitors on fibrotic diseases such as myelofibrosis and bone marrow fibrosis have been demonstrated in previous studies. The JAK inhibitor SHR0302 is a synthetic molecule that potently inhibits all members of the JAK family, particularly JAK1. However, its effect on hepatic fibrosis has not been investigated to date, to the best of our knowledge. In the present study, the effects of SHR0302 on the activation, proliferation, migration and apoptosis of hepatic stellate cells (HSCs) as well as HSC collagen production were investigated. Our data demonstrated that treatment with SHR0302 (10-9-10-5 mol/l) exerted an inhibitory effect on the activation, proliferation and migration of HSCs. In addition, the expression of collagen I and collagen III were significantly decreased following treatment with SHR0302. Furthermore, SHR0302 induced the apoptosis of HSCs, which was demonstrated by Annexin V/PI staining. SHR0302 significantly increased the activation of caspase-3 and Bax in HSCs whereas it decreased the expression of Bcl-2. SHR0302 also inhibited the activation of Akt signaling pathway. The pharmacological inhibition of the JAK1/signal transducer and activator of transcription (STAT)3 pathway led to the disruption of functions essential for HSC growth. Taken together, these findings provide evidence that SHR0302 may have the potential to alleviate hepatic fibrosis by targeting HSC functions.

摘要

属于Janus激酶(JAK)家族的蛋白酪氨酸激酶与许多细胞因子受体相关,这些受体在与配体结合后,可调节细胞的重要功能,如增殖、凋亡和分化。先前的研究已证实JAK抑制剂对骨髓纤维化和骨髓增殖性疾病等纤维化疾病具有保护作用。JAK抑制剂SHR0302是一种合成分子,能有效抑制JAK家族的所有成员,尤其是JAK1。然而,据我们所知,其对肝纤维化的影响尚未见报道。在本研究中,我们研究了SHR0302对肝星状细胞(HSC)的激活、增殖、迁移和凋亡以及HSC胶原蛋白生成的影响。我们的数据表明,用SHR0302(10-9-10-5mol/L)处理可对HSC的激活、增殖和迁移产生抑制作用。此外,用SHR0302处理后,I型和III型胶原蛋白的表达显著降低。此外,SHR0302可诱导HSC凋亡,这通过Annexin V/PI染色得以证实。SHR0302可显著增加HSC中caspase-3和Bax的激活,同时降低Bcl-2的表达。SHR0302还可抑制Akt信号通路的激活。对JAK1/信号转导子和转录激活子(STAT)3通路的药理抑制导致了对HSC生长至关重要的功能的破坏。综上所述,这些发现提供了证据,表明SHR0302可能通过靶向HSC功能来缓解肝纤维化。

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