Effect of insulin-like growth factor-1 on hyperoxia-induced apoptosis in A549 cells

JIN Zhen-Ai, ZHAO Yi-Kun, JIN Zheng-Yong, QI Hai-Feng, Mokhles Wali Gul, GONG Ming-Hua

Chinese Journal of Contemporary Pediatrics ›› 2013, Vol. 15 ›› Issue (6) : 490-493.

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Chinese Journal of Contemporary Pediatrics ›› 2013, Vol. 15 ›› Issue (6) : 490-493. DOI: 10.7499/j.issn.1008-8830.2013.06.021
EXPERIMENTAL RESEARCH

Effect of insulin-like growth factor-1 on hyperoxia-induced apoptosis in A549 cells

  • JIN Zhen-Ai, ZHAO Yi-Kun, JIN Zheng-Yong, QI Hai-Feng, Mokhles Wali Gul, GONG Ming-Hua
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Abstract

OBJECTIVE: To investigate the effect of insulin-like growth factor-1 (IGF-1), which can promote cell differentiation and inhibit cell apoptosis, on hyperoxia-induced apoptosis in A549 cells and its anti-apoptotic mechanism. METHODS: A549 cells were sub-cultured, exposed to hyperoxic conditions and were then treated with different concentrations of IGF-1 (1, 10, and 100 ng/mL) for 48 hours. Cell viability was measured by MTT assay. Cell apoptosis was evaluated by Annexin V-FITC/PI double-staining flow cytometry. Expression levels of Bax and Bcl-2 were measured by flow cytometry. RESULTS: The middle-dose and high-dose IGF-1 intervention groups had higher cell viabilities than the hyperoxic exposure group [(64±3)% and (88±4)% vs (51±3)%; P<0.05]. Compared with the air control group, the hyperoxic exposure group had a significantly higher apoptotic rate [(38.3±5.4)% vs (2.4±0.9)%; P<0.05], a significantly lower expression level of Bcl-2 [(72±5)% vs (91±4)%; P<0.05], and a significantly higher expression level of Bax [(54±6)% vs (3±2)%; P<0.05]. Compared with the hyperoxic exposure group, the low-dose, middle-dose, and high-dose IGF-1 intervention groups had significantly lower apoptotic rates [(16.1±4.7)%, (9.2±2.8)%, and (6.9±2.5)% vs (38.3±5.4)%; P<0.05], significantly higher expression level of Bcl-2 [(79±4)%, (94±4)%, and (100±5)% vs (72±5)%; P<0.05], and significantly lower expression level of Bax [(26±4)%, (5±2)%, and (4±2)% vs (54±6)%; P<0.05]. CONCLUSIONS: Hyperoxia significantly inhibits proliferation and promotes apoptosis in A549 cells. IGF-1 may promote cell proliferation and inhibit hyperoxia-induced apoptosis in A549 cells by regulating the expression of Bcl-2 and Bax.

Key words

IGF-1 / Hyperoxia / Apoptosis / A549 cell

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JIN Zhen-Ai, ZHAO Yi-Kun, JIN Zheng-Yong, QI Hai-Feng, Mokhles Wali Gul, GONG Ming-Hua. Effect of insulin-like growth factor-1 on hyperoxia-induced apoptosis in A549 cells[J]. Chinese Journal of Contemporary Pediatrics. 2013, 15(6): 490-493 https://doi.org/10.7499/j.issn.1008-8830.2013.06.021

References

[1]金贞爱,金正勇,池永学,鲁继荣.重组人胰岛素样生长因子1对高氧暴露下新生大鼠肺组织Clara细胞分泌蛋白表达的影响[J].中华儿科杂志,2007, 45(5): 369-373.

[2]Lieber M, Smith B, Szakal A, Nelson-Rees W, Todaro G. A continuous tumor-cell line from a human lung carcinoma with properties of type Ⅱalveolar epithelial  cells[J]. Int J Cancer, 1976, 17(1): 62-70.

[3]Park S, Lee YK, Jung M, Kim KH, Chung N, Ahn EK, et al. Cellular toxicity of various inhalable  metal Nano-Particles on human alveolar epithelial cells[J]. Inhal Toxicol, 2007, 19(1): 59-65.

[4]Tian D, Zhu M, Li J, Ma Y, Wu R.Cigarette smoke extract induces activation of beta-catenin/TCF signaling through inhibiting GSK3beta in human alveolar epithelial  cell line[J]. Toxicol Lett, 2009, 187(1): 58-62.

[5]朱逸,贡力,钮洪艳. 探讨MG132对人肺腺癌A549细胞凋亡的影响及其机制[J]. 中国医药导报,2011,8(34): 32-34.

[6]刘真喜,付庭焕,赵彤.IGF--1与细胞凋亡的研究进展[J]. 医学综述,2001,7(10):579-580.

[7]王华,李文斌,常立文. Mateigel胶对高氧损伤早产鼠肺泡Ⅱ型细胞黏着斑激酶表达变化及其对Ⅱ型肺泡上皮细胞增殖和凋亡的影响[J]. 中华儿科杂志,2012,50(2): 141-145.

[8]Ogunlesi F, Cho C, McGrath-Morrow SA.The effect of glutamine on A549 cells exposed to moderate hyperoxia[J]. Biochim Biophys Acta, 2004, 1688(2): 112-20.

[9]金正勇.重组Clara细胞分泌蛋白对高氧性肺损伤的影响及其机制研究[D].延边大学,2007.

[10]邹丹.Omi/HtrA2信号通路介导高氧诱导肺泡上皮细胞凋亡的作用及机制[D].泸州医学院,2011.

[11]邹新艳,董文斌,邹丹,李清平,雷小平,翟雪松,等. mitoKATP通道开放剂对高氧诱导人A549细胞凋亡的保护作用[J].中国当代儿科杂志, 2011, 13(6): 514-517.

[12]Hebishima T, Matsumoto Y, Watanabe G, Soma G, Kohchi C, Taya K, et al. Oral administration of immunopotentiator from pantoea agglomerans 1 (IP-PA1) improves the survival of B16 melanoma-inoculated Model mice[J]. Exp Anim, 2011, 60(2):101-109.

[13]徐燕,汤锦波.核因子K B诱导激酶和IK B激酶在碱性成纤维细胞生长因子作用下  基因表达及肌腱细胞增殖[J]. 中华创伤杂志, 2003, 19(6): 348-351.

[14]张兆锋,商庆新,曹谊林.体外培养肌腱细胞功能老化的观测[J].中国临床康复,2002,6(22): 3376-3377.

[15]Sun F, Liu JY, He F, Liu Z, Wang R, Wang DM, et al. In-vitro antitumor activity evaluation of hyperforin derivatives[J]. J Asian Nat Prod Res, 2011, 13(8): 688-699.

[16]Yang L, Zhou X, Yang J, Yin X, Han L, Zhao D. Aspirin inhibits cytotoxicity of peptide PrP106-126 to neuronal cells asscoiated with microglia activation in vitro[J]. J Neuroimmunol, 2008, 199(1-2): 10-17.

[17]Gradilone A, Gazzaniga P, Ribuffo D, Scarpa S, Cigna E, Vasaturo F, et al. Survivin, bcl-2, bax, and bcl-X gene expression in sentinel lymph nodes from melanoma patients[J].J Clin Oncol, 2003, 21(2): 306-312.

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