Dipartimento Biomedico di Medicina Interna e Specialistica, Sezione di Reumatologia, Università di Palermo, Palermo, Italy.
Anatomia Patologica, Ospedali Riuniti Villa Sofia-Cervello, Palermo, Italy.
Ann Rheum Dis. 2014 Aug;73(8):1566-74. doi: 10.1136/annrheumdis-2012-202925. Epub 2013 Jun 5.
Interleukin (IL)-23 has been implicated in the pathogenesis of ankylosing spondylitis (AS). The aim of the study was to clarify the mechanisms underlying the increased IL-23 expression in the gut of AS patients.
Consecutive gut biopsies from 30 HLA-B27(+) AS patients, 15 Crohn's disease (CD) patients and 10 normal subjects were obtained. Evidence for HLA-B27 misfolding was studied. Unfolded protein response (UPR) and autophagy were assessed by RT-PCR and immunohistochemistry. The contribution of UPR and autophagy in the regulation of IL-23 expression was evaluated in in vitro experiments on isolated lamina propria mononuclear cells (LPMCs).
Intracellular colocalisation of SYVN1 and FHCs but not a significant overexpression of UPR genes was observed in the gut of AS patients. Conversely, upregulation of the genes involved in the autophagy pathway was observed in the gut of AS and CD patients. Immunohistochemistry showed an increased expression of LC3II, ATG5 and ATG12 but not of SQSTM1 in the ileum of AS and CD patients. LC3II was expressed among infiltrating mononuclear cells and epithelial cells resembling Paneth cells (PC) and colocalised with ATG5 in AS and CD. Autophagy but not UPR was required to modulate the expression of IL-23 in isolated LPMCs of AS patients with chronic gut inflammation, CD patients and controls.
Our data suggest that HLA-B27 misfolding occurs in the gut of AS patients and is accompanied by activation of autophagy rather than a UPR. Autophagy appears to be associated with intestinal modulation of IL-23 in AS.
白细胞介素(IL)-23 被认为与强直性脊柱炎(AS)的发病机制有关。本研究旨在阐明 AS 患者肠道中 IL-23 表达增加的机制。
连续收集 30 例 HLA-B27(+)AS 患者、15 例克罗恩病(CD)患者和 10 例正常对照者的肠道活检组织。研究 HLA-B27 错误折叠的证据。通过 RT-PCR 和免疫组化评估未折叠蛋白反应(UPR)和自噬。在体外分离的固有层单核细胞(LPMCs)实验中评估 UPR 和自噬在调节 IL-23 表达中的作用。
在 AS 患者的肠道中观察到 SYVN1 和 FHCs 的细胞内共定位,但 UPR 基因的过度表达不明显。相反,在 AS 和 CD 患者的肠道中观察到参与自噬途径的基因上调。免疫组化显示 LC3II、ATG5 和 ATG12 的表达增加,但 SQSTM1 的表达在 AS 和 CD 患者的回肠中没有增加。LC3II 在浸润的单核细胞和上皮细胞中表达,类似于 Paneth 细胞(PC),并与 AS 和 CD 中的 ATG5 共定位。在慢性肠道炎症的 AS 患者、CD 患者和对照组的分离 LPMCs 中,自噬而非 UPR 是调节 IL-23 表达所必需的。
我们的数据表明,HLA-B27 错误折叠发生在 AS 患者的肠道中,并伴有自噬的激活,而不是 UPR。自噬似乎与 AS 患者肠道中 IL-23 的调节有关。