Umbilical Cord Cells Treatment with Metadichol® IRS Proteins and GLUT4 Expression and Implications for Diabetes

P. Raghavan
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引用次数: 4

Abstract

Insulin and IGF signaling require a family of scaffold proteins, also called as Insulin Receptor Substrate (IRS) proteins to integrate extracellular signals into intracellular responses, leading to cellular effects. Two main IRS proteins in humans are IRS1 and IRS2 and are widely expressed in most human and mammalian tissues. In this study, IRS1, IRS2, GLUT4 gene expression is quantified in Umbilical Cord (UC) cell line by semi quantitative- PCR. The internal control β-actin was used to normalize the IRS1, IRS2, GLUT4 gene expression levels. This is the first example of UC cells being induced by a ligand in expressing genes that regulate glucose and insulin levels. Metadichol® treatment at different concentrations on UC cells showed upregulation of IRS1, IRS2 and GLUT4. 100 pg/mL concentrations showed the highest upregulation of IRS1, IRS2 and GLUT4 expression. 1 ng and 100 ng/mL treatment showed marginal. Metadichol® is in addition a TNF alpha inhibitor and also inhibits Plasminogen Activation Inhibitor (PAI1) also known as SERPINE1. These genes play an important role in diabetes. The experimental results fully correlated with curated literature data using Bioinformatics software. Network analysis show the uniqueness of shared genes, IRS1, IRS2, GLUT4, TNF, PAI1, acting through multiple pathways that target multiple diseases.
用Metadichol®IRS蛋白和GLUT4表达治疗脐带细胞及其对糖尿病的影响
胰岛素和IGF信号需要一个支架蛋白家族,也称为胰岛素受体底物(IRS)蛋白,将细胞外信号整合到细胞内反应中,从而导致细胞效应。IRS1和IRS2是人类体内两种主要的IRS蛋白,它们在大多数人类和哺乳动物组织中广泛表达。本研究采用半定量PCR方法对脐带(UC)细胞株中IRS1、IRS2、GLUT4基因表达进行了定量分析。内控β-肌动蛋白用于调节IRS1、IRS2、GLUT4基因表达水平。这是UC细胞被表达调节葡萄糖和胰岛素水平的基因的配体诱导的第一个例子。不同浓度的Metadichol®处理UC细胞显示IRS1、IRS2和GLUT4上调。100 pg/mL浓度下,IRS1、IRS2和GLUT4的表达上调幅度最大。1 ng和100 ng/mL处理效果不明显。Metadichol®除了是TNF α抑制剂外,还抑制纤溶酶原激活抑制剂(PAI1),也称为SERPINE1。这些基因在糖尿病中起着重要作用。实验结果与生物信息学软件整理的文献数据完全相关。网络分析显示共享基因IRS1、IRS2、GLUT4、TNF、PAI1的独特性,它们通过多种途径作用于多种疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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