彭孝军

个人信息Personal Information

教授

博士生导师

硕士生导师

主要任职:Director, State Key laboratory of Fine Chemicals

其他任职:精细化工国家重点实验室主任、国务院学科评议组成员

性别:男

毕业院校:大连理工大学

学位:博士

所在单位:化工学院

学科:应用化学. 精细化工. 化学生物学

办公地点:大连理工大学精细化工国家重点实验室
西部校区化工实验楼F-202#  
http://peng-group.dlut.edu.cn/

联系方式:大连理工大学精细化工国家重点实验室 西部校区化工实验楼F-202 辽宁省大连市高新区凌工路2号,大连116024 Tel: 0411-84986306; Fax: 0411-84986292;课题组网址:http://peng-group.dlut.edu.cn/

电子邮箱:pengxj@dlut.edu.cn

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论文成果

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Probing the response of lung tumor cells to inflammatory microvascular endothelial cells on fluidic microdevice

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论文类型:期刊论文

发表时间:2017-01-01

发表刊物:ELECTROPHORESIS

收录刊物:SCIE、PubMed

卷号:38

期号:2

页面范围:311-319

ISSN号:0173-0835

关键字:Cell adhesion; Cell rolling; Microfluidics; Microvascular inflammation

摘要:The development of cancer depends on a complex tissue microenvironment for sustained growth, invasion, and metastasis. The extravasation of tumor cells is a critical event in tumor metastasis. However, the process and mechanism that underlie tumor cell extravasation remain unclear, which restricts the examination of many tumor processes and presents a formidable hurdle to drug development. To explore the initial steps by which lung tumor cells interact with the brain microvascular wall in the course of extravasation, we present a simple, inexpensive, and time-saving microfluidic device to mimic the inflammatory brain microvascular microenvironment and to investigate both the biochemical and mechanical causes of lung tumor cell rolling and adhesion on inflammatory endothelium to analyze the synergistic effects on tumor extravasation under fluidic shear stress conditions. Under microvascular inflammation induced by tumor necrosis factor , the lung tumor cells (A549 cells) displayed significant adhesion activity. In addition, we found that this situation could be reversed by administration of Rho/Rho-associated protein serine/threonine kinase (ROCK) inhibitor (Y27632). We believe that this promising microdevice-based tumor adhesion and extravasation research platform can be used to study tumor behavior in an inflammatory vascular system and will make a valuable contribution for the investigation of the mechanism of tumor cell extravasation.