Department of Human Pathology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.
J Clin Pathol. 2014 Jun;67(6):470-6. doi: 10.1136/jclinpath-2013-201917. Epub 2014 Jan 9.
Serum antimitochondrial antibodies are characteristic in most patients with primary biliary cirrhosis (PBC); however, the significance of antimitochondrial antibodies in the pathogenesis of PBC remains unclear. We examined the extent and types of mitochondrial protein-expressing inflammatory cells and its association with deregulated autophagy of mitochondria in biliary epithelial lesions in PBC.
We examined the expression of pyruvate dehydrogenase complex-E2 component and a mitochondrial protein cytochrome c oxidase, subunit I in inflammatory cells in livers taken from patients with PBC (n=35) and control livers (n=64) including primary sclerosing cholangitis. Mitochondrial protein-expressing inflammatory cells were characterised by double immunofluorescence with surface markers.
Infiltration of mitochondrial protein-expressing inflammatory cells was mainly observed in portal tracts and in the biliary epithelial layer and around the damaged small bile ducts in PBC. The extent of infiltration in portal tracts was significantly higher in PBC and early stage of chronic viral hepatitis than normal livers. The extent of infiltration around bile ducts and in biliary epithelial layer was significantly higher in early stage of PBC than control livers. Mitochondrial protein-expressing inflammatory cells included (1) CD68 and/or myeloperoxidase -positive monocytes/macrophages and (2) CD79a, CD38, CD138, IgM-positive and/or IgG-positive plasma cells. Colocalised expression of pyruvate dehydrogenase complex-E2 component and autophagy marker light chain 3β was observed in the inflammatory cells.
Mitochondrial protein-expressing inflammatory cells infiltrating around the damaged bile ducts and in biliary epithelial layers may be closely associated with the pathogenesis of bile duct lesion in PBC.
血清抗线粒体抗体在大多数原发性胆汁性肝硬化(PBC)患者中具有特征性;然而,抗线粒体抗体在 PBC 发病机制中的意义仍不清楚。我们检查了 PBC 胆管上皮病变中线粒体蛋白表达炎症细胞的程度和类型及其与线粒体自噬失调的关系。
我们检查了来自 PBC 患者(n=35)和对照肝脏(n=64)的肝脏中丙酮酸脱氢酶复合物-E2 成分和线粒体蛋白细胞色素 c 氧化酶亚基 I 在炎症细胞中的表达,包括原发性硬化性胆管炎。用表面标志物对线粒体蛋白表达的炎症细胞进行双重免疫荧光染色。
在 PBC 中,主要观察到线粒体蛋白表达的炎症细胞浸润在门脉区和胆管上皮层以及受损的小胆管周围。门脉区浸润的程度在 PBC 和慢性病毒性肝炎的早期阶段明显高于正常肝脏。胆管周围和胆管上皮层的浸润程度在 PBC 的早期阶段明显高于对照肝脏。线粒体蛋白表达的炎症细胞包括(1)CD68 和/或髓过氧化物酶阳性单核细胞/巨噬细胞和(2)CD79a、CD38、CD138、IgM 阳性和/或 IgG 阳性浆细胞。在炎症细胞中观察到丙酮酸脱氢酶复合物-E2 成分和自噬标记物 LC3β的共表达。
浸润在受损胆管周围和胆管上皮层中的表达线粒体蛋白的炎症细胞可能与 PBC 胆管损伤的发病机制密切相关。