Gamma-secretase-independent role for cadherin-11 in neurotrophin receptor p75 (p75NTR) mediated glioblastoma cell migration

被引:13
|
作者
Berghoff, Janina [1 ]
Jaisimha, Anirudh Vinay [1 ]
Duggan, Stephen [1 ]
MacSharry, John [2 ,3 ]
McCarthy, Justin V. [1 ]
机构
[1] Natl Univ Ireland Univ Coll Cork, ABCRF, Sch Biochem & Cell Biol, Signal Transduct Lab, Cork, Ireland
[2] Natl Univ Ireland Univ Coll Cork, Sch Med, APC Microbiome Inst, Cork, Ireland
[3] Natl Univ Ireland Univ Coll Cork, Sch Microbiol, Cork, Ireland
基金
爱尔兰科学基金会;
关键词
P75 neurotrophin receptor; Gamma-secretase; Regulated intramembrane proteolysis; Glioblastoma multiforme; Glioma; Migration; Cadherin-11; REGULATED INTRAMEMBRANE PROTEOLYSIS; INTRACELLULAR DOMAIN; NUCLEAR TRANSLOCATION; DEPENDENT CLEAVAGE; SUPPRESSES GROWTH; UP-REGULATION; SURVIVAL; ACTIVATION; EXPRESSION; INVASION;
D O I
10.1016/j.mcn.2015.10.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The p75 neurotrophin receptor (p75(NTR)) undergoes gamma-secretase-mediated regulated intramembrane proteolysis and is involved in glioblastoma cell migration and invasion. Consistent with previous reports, in this study we show that p75NTR increases U87-MG glioblastoma cell migration, which is reversed by inhibition of gamma-secretase activity. However, we show that expression or stabilization of the gamma-secretase-generated p75(NTR) intracellular domain (ICD) is not sufficient to induce U87-MG glioblastoma cell migration, and that exogenous expression of p75(NTR) ICD inhibits p75(NTR)-mediated glioblastoma cell (U87-MG and U373-MG) migration. To identify pathways and to determine how p75(NTR) mediates glioblastoma migration we utilized a microarray approach to assess differential gene expression profiles between parental U87-MG and cells stably expressing wild-type p75(NTR), a gamma-secretase cleavage-resistant chimeric p75(NTR) mutant (p75FasTM) and the gamma-secretase-generated p75(NTR)-ICD, which mimics constitutively cleaved p75(NTR) receptor. In our microarray data analysis we identified a subset of genes that were constitutively up-regulated in wild-type p75(NTR) cells, which were also repressed in p75(NTR) ICD expressing cells. Furthermore, our data revealed among the many differentially expressed genes, cadherin-11 (Cdh-11), matrix metalloproteinase 12 and relaxin/insulin-like family peptide receptor 2 as constitutively up-regulated in wild-type p75(NTR) cells, independent of gamma-secretase activity. Consistent with a role in glioblastoma migration, we found that U87-p75(NTR) cells express higher levels of Cdh-11 protein and that siRNA-mediated knockdown of Cdh-11 resulted in a significant decrease in p75NTR-mediated glioblastoma cell migration. Therefore, we hypothesize that p75(NTR) can impact U87-MG glioblastoma cell migration in a gamma-secretase-independent manner through modulation of specific genes. including Cdh-11, and that both gamma-secretase-independent and -dependent mechanisms are involved in p75(NTR)-mediated U87-MG glioblastoma cell migration. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:41 / 53
页数:13
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