A novel extracellular Hsp90 mediated co-receptor function for LRP1 regulates EphA2 dependent glioblastoma cell invasion.

A novel extracellular Hsp90 mediated co-receptor function for LRP1 regulates EphA2 dependent glioblastoma cell invasion.
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DOI:
10.1371/journal.pone.0017649
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发表时间:
2011-03-08
期刊:
影响因子:
3.7
通讯作者:
Isaacs JS
Isaacs JS
中科院分区:
综合性期刊3区
文献类型:
--
作者:
Gopal U;Bohonowych JE;Lema-Tome C;Liu A;Garrett-Mayer E;Wang B;Isaacs JS

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细胞外Hsp 90蛋白(eHsp 90)通过一种知之甚少的机制增强癌细胞的运动性和侵袭性,该机制涉及配体介导的与其同源受体LRP 1的功能。多形性胶质母细胞瘤(GBM)是最具侵袭性和致命性的脑癌之一。受体酪氨酸激酶EphA 2在大多数GBM样本中过表达,并且通过其在S897处的EphA 2的AKT依赖性激活(P-EphA 2S 897)而成为GBM侵袭性的关键介质。我们探索了eHsp 90是否可以通过调节EphA 2介导的信号传导而赋予GBM侵袭性。我们发现eHsp 90信号传导对于维持AKT活化、P-EphA 2S 897、板状伪足形成以及伴随的GBM细胞运动和侵袭是必不可少的。此外,eHsp 90以AKT依赖性方式促进LRP 1向EphA 2的募集。这一发现得到了生物化学方法学以及LRP 1和P-EphA 2S 897在原发性和复发性GBM肿瘤标本中的双重表达的支持。此外,低氧介导的GBM运动和侵袭的促进作用依赖于eHsp 90-LRP 1信号传导。缺氧显著升高eHsp 90和LRP 1的表面表达,伴随着src、AKT和EphA 2的eHsp 90依赖性活化。我们在此证明了涉及EphA 2功能的eHsp 90-LRP 1依赖性调节的新的串扰机制。我们强调了eHsp 90在通过LRP 1转导信号传导和促进EphA 2的LRP 1共受体功能中的双重作用。综上所述,我们的结果表明eHsp 90-LRP 1信号轴的激活是AKT信号传导和EphA 2激活的启动和维持中的一个必要步骤,从而暗示该途径是促进GBM侵袭性的一个组成部分。
Extracellular Hsp90 protein (eHsp90) potentiates cancer cell motility and invasion through a poorly understood mechanism involving ligand mediated function with its cognate receptor LRP1. Glioblastoma multiforme (GBM) represents one of the most aggressive and lethal brain cancers. The receptor tyrosine kinase EphA2 is overexpressed in the majority of GBM specimens and is a critical mediator of GBM invasiveness through its AKT dependent activation of EphA2 at S897 (P-EphA2S897). We explored whether eHsp90 may confer invasive properties to GBM via regulation of EphA2 mediated signaling. We find that eHsp90 signaling is essential for sustaining AKT activation, P-EphA2S897, lamellipodia formation, and concomitant GBM cell motility and invasion. Furthermore, eHsp90 promotes the recruitment of LRP1 to EphA2 in an AKT dependent manner. A finding supported by biochemical methodology and the dual expression of LRP1 and P-EphA2S897 in primary and recurrent GBM tumor specimens. Moreover, hypoxia mediated facilitation of GBM motility and invasion is dependent upon eHsp90-LRP1 signaling. Hypoxia dramatically elevated surface expression of both eHsp90 and LRP1, concomitant with eHsp90 dependent activation of src, AKT, and EphA2. We herein demonstrate a novel crosstalk mechanism involving eHsp90-LRP1 dependent regulation of EphA2 function. We highlight a dual role for eHsp90 in transducing signaling via LRP1, and in facilitating LRP1 co-receptor function for EphA2. Taken together, our results demonstrate activation of the eHsp90-LRP1 signaling axis as an obligate step in the initiation and maintenance of AKT signaling and EphA2 activation, thereby implicating this pathway as an integral component contributing to the aggressive nature of GBM.
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