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一种基于细胞的、带有干扰素刺激基因15启动子的干扰素-τ检测方法。

A cell-based interferon-tau assay with an interferon-stimulated gene 15 promoter.

作者信息

Toji Noriyuki, Koshi Katsuo, Furusawa Tadashi, Takahashi Toru, Ishiguro-Oonuma Toshina, Kizaki Keiichiro, Hashizume Kazuyoshi

机构信息

Cooperative Department of Veterinary Medicine, Faculty of Agriculture, Iwate University.

The United Graduate School of Vaterinary Sciences, Gifu University.

出版信息

Biomed Res. 2018;39(1):13-20. doi: 10.2220/biomedres.39.13.

Abstract

Interferon-tau (IFNT) is known as an early pregnancy recognition signal in ruminants. An accurate and convenient IFNT detection system is desirable for the diagnosis of endometrial and trophoblastic functions, including gestation status, in cows. The aim of this study was to develop a new cell-based assay, which involved the stable introduction of an interferon-stimulated gene promoter to a luciferase reporter system. The reactivity of four interferon-stimulated genes to IFNT in Madin-Darby bovine kidney (MDBK) cells was confirmed using reverse transcription-quantitative PCR. The upstream region of the interferon-stimulated gene 15 ubiquitin-like modifier (ISG15) gene as the promoter of the reporter gene, which is more responsive to IFNT and other IFNs, was determined using the luciferase assay. The reporter gene with the ISG15 upstream region was stably transfected into MDBK cells using the PiggyBac vector system; this cell line responded to type I IFNs in a dose-dependent manner. Because of its convenience, this cell line is suitable for the quantification of IFNT as well as other type I IFNs activities.

摘要

干扰素τ(IFNT)在反刍动物中被认为是一种早期妊娠识别信号。对于奶牛子宫内膜和滋养层功能(包括妊娠状态)的诊断而言,需要一种准确且便捷的IFNT检测系统。本研究的目的是开发一种新的基于细胞的检测方法,该方法涉及将干扰素刺激基因启动子稳定导入荧光素酶报告系统。使用逆转录定量PCR在马-达二氏牛肾(MDBK)细胞中确认了四种干扰素刺激基因对IFNT的反应性。使用荧光素酶测定法确定了干扰素刺激基因15泛素样修饰物(ISG15)基因的上游区域作为报告基因的启动子,该区域对IFNT和其他干扰素更敏感。使用PiggyBac载体系统将具有ISG15上游区域的报告基因稳定转染到MDBK细胞中;该细胞系对I型干扰素呈剂量依赖性反应。由于其便利性,该细胞系适用于IFNT以及其他I型干扰素活性的定量分析。

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