French S W, Mendoza A S, Afifiyan N, Tillman B, Vitocruz E, French B A
Department of Pathology, Harbor-UCLA Medical Center, Los Angeles BioMedical Institute, 1000 W. Carson St., Torrance, CA 90509, United States.
Department of Pathology, Harbor-UCLA Medical Center, Los Angeles BioMedical Institute, 1000 W. Carson St., Torrance, CA 90509, United States.
Exp Mol Pathol. 2017 Oct;103(2):137-140. doi: 10.1016/j.yexmp.2017.08.005. Epub 2017 Aug 14.
IL-8 (C-X-L motif chemokine ligase 8) and CXCR2 (C-X-C-motif chemokine receptor 2) are up regulated in alcoholic hepatitis (AH) liver biopsies. One of the consequences is the attraction and chemotactic neutrophilic infiltrate seen at the AH stage of alcoholic liver disease.
Human formalin-fixed, paraffin-embedded (FFPE) liver biopsies from patients who have AH were studied by (2.1) RNA sequencing, (2.2) PCR and (2.3) semi quantitation of specific proteins in biopsy sections using immunohistochemical measurements of antibody fluorescent intensity with morphometric technology.
Immunohistochemistry of IL-8 showed that the expression was increased in the cytoplasm of the hepatocytes in AH liver biopsies compared to the controls. IL-8 and ubiquitin were co-localized in the MDBs. Numerous neutrophils were found throughout and satellitosis of neutrophils around MDBs was present. This suggested that IL-8 may be involved in MDB pathogenesis. RNA seq analysis revealed activation by IL-8 which included neutrophil chemotaxis by LIM domain kinase 2 (LIMK2) (17.5 fold increase) and G protein subunit alpha 15 (GNA15) (27.8 fold increase).
The formation of MDBs by liver cells showed colocalization of ubiquitin and IL-8 in the MDBs. This suggested that IL-8 in these hepatocytes attracted the neutrophils to form satellitosis. This correlated with up regulation of the proteins downstream from the IL-8 pathways including LIMK2, GNG2 (guanine nucleotide binding proteins) and PIK3CB (phosphatidyl isitol-4, 5-biophosphate-3-kinase, catalytic subunit beta).
白细胞介素-8(C-X-L基序趋化因子配体8)和CXC趋化因子受体2(CXCR2)在酒精性肝炎(AH)肝活检中表达上调。其中一个后果是在酒精性肝病的AH阶段出现吸引和趋化性中性粒细胞浸润。
对患有AH的患者的人福尔马林固定、石蜡包埋(FFPE)肝活检组织进行了如下研究:(2.1)RNA测序,(2.2)聚合酶链反应,以及(2.3)使用形态计量技术通过抗体荧光强度的免疫组织化学测量对活检切片中的特定蛋白质进行半定量分析。
白细胞介素-8的免疫组织化学显示,与对照组相比,AH肝活检组织中肝细胞胞质内的表达增加。白细胞介素-8和泛素在 Mallory-Denk 小体(MDBs)中共定位。在整个组织中发现了大量中性粒细胞,并且在MDBs周围存在中性粒细胞的卫星现象。这表明白细胞介素-8可能参与了MDB的发病机制。RNA序列分析显示白细胞介素-8激活了包括由LIM结构域激酶2(LIMK2)(增加17.5倍)和G蛋白亚基α15(GNA15)(增加27.8倍)介导的中性粒细胞趋化作用。
肝细胞形成的MDBs显示泛素和白细胞介素-8在MDBs中共定位。这表明这些肝细胞中的白细胞介素-8吸引中性粒细胞形成卫星现象。这与白细胞介素-8途径下游的蛋白质上调相关,包括LIMK2、GNG2(鸟嘌呤核苷酸结合蛋白)和PIK3CB(磷脂酰肌醇-4,5-二磷酸-3-激酶,催化亚基β)。