FN14 mRNA Expression Correlates with an Increased Number of Veins during Angiogenesis in the Process of Liver Fibrosis.

IF 1.5 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Elena I Lebedeva, Andrei S Babenka, Pelin Hastemir, Anatoliy T Shchastniy, Dmitry A Zinovkin, Md Zahidul Islam Pranjol
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引用次数: 0

Abstract

In this study, we hypothesize that angiogenesis of special hepatic vessels such as sinusoid capillaries or veins is closely associated with increasing production of connective tissue in fibrogenesis. Thirty-six male Wistar rats were induced with hepatitis and cirrhosis of the liver using thioacetamide. The number of sinusoidal capillaries, veins, arteries and the area of connective tissue were counted and determined. Immunohistochemical study was performed on paraffin sections using monoclonal mouse anti-CD31. mRNA expression was determined using qPCR. We found a statistically significant reduction in the number of sinusoidal capillaries (p<0.0001) and an increase in the number of interlobular veins (p<0.0001) in the fibrosis and cirrhosis groups compared to the control group. There are no differences in the number of interlobular arteries (p=0.282) in the three groups. In our analysis, we found that the expression (mRNA) of Fn14 correlated with the number of veins in liver fibrosis (r=0.44, p=0.008). Our data shows that modulation of veins angiogenesis during fibrosis in chronic liver diseases may play an important role in increasing pathological changes of the liver.

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肝纤维化过程中血管生成过程中FN14mRNA表达与静脉数量增加相关。
在这项研究中,我们假设特殊肝血管(如血窦毛细血管或静脉)的血管生成与纤维化过程中结缔组织生成的增加密切相关。用硫代乙酰胺诱导36只雄性Wistar大鼠发生肝炎和肝硬化。对正弦毛细血管、静脉、动脉的数量和结缔组织的面积进行计数和测定。使用单克隆小鼠抗CD31对石蜡切片进行免疫组织化学研究。使用qPCR测定mRNA表达。我们发现正弦毛细血管的数量在统计学上显著减少(p
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来源期刊
CiteScore
3.60
自引率
0.00%
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0
期刊介绍: The International Journal of Molecular and Cellular Medicine (IJMCM) is a peer-reviewed, quarterly publication of Cellular and Molecular Biology Research Center (CMBRC), Babol University of Medical Sciences, Babol, Iran. The journal covers all cellular & molecular biology and medicine disciplines such as the genetic basis of disease, biomarker discovery in diagnosis and treatment, genomics and proteomics, bioinformatics, computer applications in human biology, stem cells and tissue engineering, medical biotechnology, nanomedicine, cellular processes related to growth, death and survival, clinical biochemistry, molecular & cellular immunology, molecular and cellular aspects of infectious disease and cancer research. IJMCM is a free access journal. All open access articles published in IJMCM are distributed under the terms of the Creative Commons Attribution CC BY. The journal doesn''t have any submission and article processing charges (APCs).
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