Suppr超能文献

10 M-T7: measuring chemokine-modulating activity.

作者信息

Bartee Mee Y, Dai Erbin, Liu Liying, Munuswamy-Ramanujam Ganesh, Macaulay Colin, McIvor Dana, McFadden Grant, Lucas Alexandra R

机构信息

Division of Cardiovascular Medicine, Department of Medicine, University of Florida, Gainesville, Florida, USA.

出版信息

Methods Enzymol. 2009;460:209-28. doi: 10.1016/S0076-6879(09)05210-0.

Abstract

Chemokines are important for activation of a host of cellular immune and inflammatory responses including cell signaling, activation, and communication. M-T7, a myxoma virus protein, inhibits the activity of chemokines by direct binding to chemokines and/or with glycosaminoglycans (GAGs). To study the effects of this chemokine-modulating protein (CMP), we use a variety of in vitro and in vivo techniques to evaluate M-T7 inhibition of inflammatory cells. To quickly analyze the effects of M-T7, changes in cell adhesion and membrane fluidity are measured as well as cell migration in mouse ascites. For more physiological analyses, an aortic transplant model in rodents is used to assess change in inflammatory cell infiltrates and vascular plaque growth (rejection). Utilization of the combination of these in vitro and in vivo techniques allows for a more complete study of the chemokine-modulating activity of M-T7, and can be used to study other immune and inflammation-modulating proteins.

摘要

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验