Overexpression of osteopontin induces angiogenesis of endothelial progenitor cells via the avβ3/PI3K/AKT/eNOS/NO signaling pathway in glioma cells

被引：104

作者：

Wang, Yingyi ^{[1
]}

Yan, Wei ^{[1
]}

Lu, Xiaoming ^{[1
]}

Qian, Chunfa ^{[2
]}

Zhang, Junxia ^{[1
]}

Li, Ping ^{[1
]}

Shi, Lei ^{[3
]}

Zhao, Peng ^{[1
]}

Fu, Zhen ^{[1
]}

Pu, Peiyu ^{[4
]}

Kang, Chunshen ^{[4
]}

Jiang, Tao ^{[5
]}

Liu, Ning ^{[1
]}

You, Yongping ^{[1
]}

机构：

[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Neurosurg, Nanjing 210029, Peoples R China

[2] Nanjing Med Univ, Affiliated Brain Hosp, Dept Neurosurg, Nanjing 210029, Peoples R China

[3] Jiangsu Univ, Peoples Hosp Kunshan 1, Dept Neurosurg, Suzhou 215300, Peoples R China

[4] Tianjin Med Univ, Gen Hosp, Dept Neurosurg, Tianjin 300052, Peoples R China

[5] Capital Med Univ, Glioma Therapy Ctr, Beijing Tiantan Hosp, Beijing 100050, Peoples R China

来源：

EUROPEAN JOURNAL OF CELL BIOLOGY | 2011年 / 90卷 / 08期

关键词：

Glioma; Osteopontin; Angiogenesis; NITRIC-OXIDE SYNTHASE; GASTRIC-CANCER; GROWTH-FACTORS; EXPRESSION; ENOS; INHIBITION; ISCHEMIA; MODEL;

D O I：

10.1016/j.ejcb.2011.03.005

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

Angiogenesis, a hallmark of tumor growth, is regulated by various angiogenic factors. Recent studies have shown that osteopontin (OPN) is a secreted, integrin-binding protein that contributes to glioma progression. However, its effect on the angiogenesis of gliomas is not fully understood. To elucidate the role of OPN in the process of glioma angiogenesis, endothelial progenitor cells (EPCs) were treated with conditioned media of human glioma SHG44 cells overexpressing OPN. Here, we identified that OPN secreted by glioma cells accelerated EPCs angiogenesis in vitro, including proliferation, migration, and tube formation. OPN also induced the activation of Ala and endothelial nitric oxide synthase (eNOS) and increased NO production without affecting the expression of VEGF, VEGFR-1, or VEGFR-2. Moreover, the av beta 3 antibody, the PI3-K inhibitor LY294002 and the eNOS inhibitor NMA suppressed the OPN-mediated increase in NO production and angiogenesis in EPCs. Taken together, these results demonstrate that OPN directly stimulates angiogenesis via the av beta 3/PI3-K/AKT/eNOS/NO signaling pathway and may play an important role in tumorigenesis by enhancing angiogenesis in gliomas. (C) 2011 Elsevier GmbH. All rights reserved.

引用

页码：642 / 648

页数：7

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