Platelet activation during tumor development, the potential role of BDNF-TrkB autocrine loop

被引:29
作者
Yang, Zhen Fan [1 ]
Ho, David W. [1 ]
Lau, Chi Keung [1 ]
Tam, Ka Ho [1 ]
Lam, Chi Tat [1 ]
Poon, Ronnie T. P. [1 ]
Fan, Sheung Tat [1 ]
机构
[1] Univ Hong Kong, Ctr Study Liver Dis, Dept Surg, Hong Kong, Hong Kong, Peoples R China
关键词
platelet; brain-derived neurotrophic factor; tyrosine kinase receptor B; hepatocellular carcinoma;
D O I
10.1016/j.bbrc.2006.06.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Platelets are an important place for the storage of angiogenic factors, such as vascular endothelial growth factor (VEGF) and brain-derived neurotrophic factor (BDNF). The present study aims to investigate the interaction between BDNF-TrkB pathway and platelet activation during tumor development. In an orthotopic hepatocellular carcinoma (HCC) model, increased levels of serum and plasma BDNF were detected with tumor progression. Higher numbers of CD62P(+) and TrkB(+) platelets were found in the tumor-bearing rats. In the in vitro setting, tumor-conditioned-medium (TCM) and BDNF recombinant protein stimulated CD62P upregulation and subsequent BDNF release in the freshly isolated platelets, whereas this effect could be inhibited by TrkB blockade. TCM and BDNF culture augmented the expression of heat shock protein 90 (Hsp90) in the platelets, which could be reversed by TrkB blockade. In conclusion, this study suggested the presence of BDNF-TrkB autocrine loop in platelets and its importance in regulating platelet activation during tumor development. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:981 / 985
页数:5
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