Cigarette smoke extract reduces VEGF in primary human airway epithelial cells

被引:34
|
作者
Thaikoottathil, J. V. [1 ]
Martin, R. J. [1 ]
Zdunek, J. [1 ]
Weinberger, A. [1 ]
Rino, J. G. [1 ]
Chu, H. W. [1 ]
机构
[1] Natl Jewish Hlth, Dept Med, Denver, CO USA
关键词
Airway epithelial cells; cigarette smoke extract; extracellular signal-regulated kinase 1/2; protein kinase C; vascular endothelial growth factor; ENDOTHELIAL GROWTH-FACTOR; PROTEIN-KINASE-C; PROINFLAMMATORY CYTOKINE RELEASE; RESPIRATORY-TRACT INFECTIONS; KAPPA-B ACTIVATION; OXIDATIVE STRESS; BACTERIAL-COLONIZATION; FACTOR RECEPTOR-2; MESSENGER-RNA; UP-REGULATION;
D O I
10.1183/09031936.00080708
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Reduced vascular endothelial growth factor (VEGF) has been reported In bronchoalveolar lavage fluid and lungs of severe emphysema patients. Airway epithelial cells (AEC) are exposed to various environmental Insults like cigarette smoke and bacterial Infections, but their direct effect on VEGF production in well-differentiated primary human AEC remains unclear. The current authors determined the effect of cigarette smoke extract (CSE) alone and In combination with Mycoplasma pneumoniae (Mp) on VEGF production In well-differentiated primary normal human bronchial epithelial (NHBE) and small airway epithelial cells (SAEC) in air-liquid Interface cultures. Secretion and expression of VEGF were determined by ELISA and real-time RT-PCR, respectively. Cell growth, apoptosis, extracellular signal-regulated kinase (ERK)1/2 and protein kinase (PK)C signalling pathways were evaluated to further dissect VEGF regulation under CSE treatment. CSE significantly reduced VEGF secretion In NHBE and SAEC. In SAEC, Mp alone significantly increased the VEGF, while the presence of CSE attenuated Mp-induced VEGF production. While ERK inhibitor reduced VEGF secretion only in NHBE, a PKC inhibitor significantly decreased VEGF secretion In both NHBE and SAEC. In conclusion, direct cigarette smoke extract exposure significantly reduced vascular endothelial growth factor production in well-differentiated primary human airway epithelial cells, In part through modifying extracellular signal-regulated kinase 1/2 and protein kinase C signalling pathways.
引用
收藏
页码:835 / 843
页数:9
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