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β-arrestin 1 调节原发性胆汁性肝硬化患者自身免疫 T 细胞的功能。

β-Arrestin 1 modulates functions of autoimmune T cells from primary biliary cirrhosis patients.

机构信息

Department of Laboratory Diagnostic, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai, 200003, China.

出版信息

J Clin Immunol. 2011 Jun;31(3):346-55. doi: 10.1007/s10875-010-9492-4. Epub 2011 Jan 18.

Abstract

OBJECTIVES

Primary biliary cirrhosis (PBC) is an autoimmune disease, characterized by antimitochondrial antibodies and autoreactive T cells causing destruction of the primary bile ducts. The molecular mechanisms regulating the autoreactive T cells remain elusive. β-Arrestins (βarr) are multifunctional signaling molecules that are crucial to T cell survival. We hypothesized that βarr plays a critical regulatory function in the autoreactive T cells of PBC patients.

METHODS

Patients with hepatic biliary cirrhosis (n=60) were evaluated. Cytokine expression, T cell proliferation, and transcription factors were evaluated to assess regulatory functions in autoreactive T cells from the patient.

RESULTS

Our studies showed that expression of βarr1 was elevated significantly in T lymphocytes from patients with PBC. Moreover, the level of βarr1 mRNA positively correlated with Mayo risk score in PBC patients. Based on modulation of βarr in autoreactive T cell lines, overexpression of βarr1 increased T cell proliferation, augmented interferon production, downregulated activities of nuclear factor κB and AP-1, promoted acetylation of histone H4 in the promoter regions of CD40L, LIGHT, IL-17 and interferon-γ, while downregulating acetylation of histone H4 in the promoter regions of TRAIL, Apo2, and HDAC7A, thereby regulating expression of these genes.

CONCLUSIONS

Our findings suggest that βarr1 contributes to the pathogenesis of PBC, having significant implications for novel therapy strategy, further providing information for investigating the mechanisms of autoimmune disease.

摘要

目的

原发性胆汁性肝硬化(PBC)是一种自身免疫性疾病,其特征是抗线粒体抗体和自身反应性 T 细胞导致原发性胆管破坏。调节自身反应性 T 细胞的分子机制仍不清楚。β- arrestins(βarr)是多功能信号分子,对 T 细胞存活至关重要。我们假设βarr 在 PBC 患者的自身反应性 T 细胞中发挥关键的调节功能。

方法

评估了 60 例肝胆汁性肝硬化患者。评估细胞因子表达、T 细胞增殖和转录因子,以评估患者自身反应性 T 细胞的调节功能。

结果

我们的研究表明,PBC 患者 T 淋巴细胞中βarr1 的表达显著升高。此外,βarr1mRNA 水平与 PBC 患者的 Mayo 风险评分呈正相关。基于对自身反应性 T 细胞系中βarr 的调节,βarr1 的过表达增加了 T 细胞增殖,增加了干扰素的产生,下调了核因子κB 和 AP-1 的活性,促进了 CD40L、LIGHT、IL-17 和干扰素-γ启动子区域组蛋白 H4 的乙酰化,同时下调了 TRAIL、Apo2 和 HDAC7A 启动子区域组蛋白 H4 的乙酰化,从而调节这些基因的表达。

结论

我们的研究结果表明,βarr1 参与了 PBC 的发病机制,这对新的治疗策略具有重要意义,进一步为研究自身免疫性疾病的机制提供了信息。

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