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前胶原C蛋白酶增强子1(PCPE-1)作为小鼠肌肉和肝纤维化的血浆标志物

Procollagen C-Proteinase Enhancer 1 (PCPE-1) as a Plasma Marker of Muscle and Liver Fibrosis in Mice.

作者信息

Hassoun Eyal, Safrin Mary, Ziv Hana, Pri-Chen Sarah, Kessler Efrat

机构信息

Maurice and Gabriela Goldschleger Eye Research Institute, Tel-Aviv University Sackler Faculty of Medicine, Sheba Medical Center, Tel-Hashomer, 52621, Israel.

出版信息

PLoS One. 2016 Jul 26;11(7):e0159606. doi: 10.1371/journal.pone.0159606. eCollection 2016.

DOI:10.1371/journal.pone.0159606
PMID:27458976
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4961444/
Abstract

Current non-invasive diagnostic methods of fibrosis are limited in their ability to identify early and intermediate stages of fibrosis and assess the efficacy of therapy. New biomarkers of fibrosis are therefore constantly sought for, leading us to evaluate procollagen C-proteinase enhancer 1 (PCPE-1), a fibrosis-related extracellular matrix glycoprotein, as a plasma marker of fibrosis. A sandwich ELISA that permitted accurate measurements of PCPE-1 concentrations in mouse plasma was established. Tissue fibrosis was assessed using histochemical, immunofluorescence, and immunoblotting analyses for type I collagen and PCPE-1. The normal plasma concentration of PCPE-1 in 6 weeks to 4 months old mice was ~200 ng/ml (189.5 ± 11.3 to 206.8 ± 13.8 ng/ml). PCPE-1 plasma concentrations in four and 8.5 months old mdx mice displaying fibrotic diaphragms increased 27 and 40% respectively relatively to age-matched control mice, an increase comparable to that of the N-propeptide of procollagen type III (PIIINP), a known blood marker of fibrosis. PCPE-1 plasma levels in mice with CCl4-induced liver fibrosis increased 34 to 50% relatively to respective controls and reflected the severity of the disease, namely increased gradually during the progression of fibrosis and went down to basal levels during recovery, in parallel to changes in the liver content of collagen I and PCPE-1. The results favor PCPE-1 as a potential new clinically valuable fibrosis biomarker.

摘要

目前用于诊断纤维化的非侵入性方法在识别纤维化的早期和中期阶段以及评估治疗效果方面能力有限。因此,人们一直在不断寻找新的纤维化生物标志物,这促使我们评估原胶原C蛋白酶增强子1(PCPE-1),一种与纤维化相关的细胞外基质糖蛋白,作为纤维化的血浆标志物。建立了一种夹心ELISA法,可准确测量小鼠血浆中PCPE-1的浓度。使用针对I型胶原和PCPE-1的组织化学、免疫荧光和免疫印迹分析来评估组织纤维化。6周龄至4月龄小鼠的PCPE-1正常血浆浓度约为200 ng/ml(189.5±11.3至206.8±13.8 ng/ml)。与年龄匹配的对照小鼠相比,患有纤维化膈肌的4月龄和8.5月龄mdx小鼠的PCPE-1血浆浓度分别增加了27%和40%,这一增加幅度与已知的纤维化血液标志物III型前胶原N端前肽(PIIINP)相当。四氯化碳诱导的肝纤维化小鼠的PCPE-1血浆水平相对于各自的对照组增加了34%至50%,并反映了疾病的严重程度,即在纤维化进展过程中逐渐升高,在恢复过程中降至基础水平,这与肝脏中I型胶原和PCPE-1含量的变化平行。这些结果表明PCPE-1是一种潜在的具有临床价值的新型纤维化生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a089/4961444/b84c29061058/pone.0159606.g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a089/4961444/b84c29061058/pone.0159606.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a089/4961444/c7bd0f03df87/pone.0159606.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a089/4961444/cad9e7ce4c67/pone.0159606.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a089/4961444/67ffe3d36b86/pone.0159606.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a089/4961444/03371f8226b2/pone.0159606.g004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a089/4961444/b84c29061058/pone.0159606.g006.jpg

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PCPE-1, a brown adipose tissue-derived cytokine, promotes obesity-induced liver fibrosis.PCPE-1,一种来源于棕色脂肪组织的细胞因子,可促进肥胖诱导的肝纤维化。
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