Zhi-Su Liu1, Sheng-Li Tang, Zhong-Li Ai. 1. Department of General Surgery, Zhongnan Hospital of Wuhan University, Wuhan 430071, Hubei Province, China. hyfr@mail.wh.cei.gov.cn
Abstract
AIM: To study the effect of hydroxyapatite (HAP) nanoparticles on human hepatoma cell line BEL-7402 in vitro. METHODS: The human hepatoma cell line BEL-7402 was cultured and treated with HAP nanoparticles at various concentrations. Growth suppression was detected with MTT colorimetric assay, cell apoptotic alterations were evaluated by cytochemical staining (Hoechst 33258), transmission electron microscopy (TEM), and flow cytometry (FCM). RESULTS: HAP nanoparticles inhibited the growth of hepatoma cells in a dose-dependent manner, with IC(50) values of 29.30 mg/L. Treated with 50-200 mg/L HAP nanoparticles for 48 h, BEL-7402 cells apoptosis with nuclear chromatin condensation and fragmentation as well as cell shrinkage and the formation of apoptotic bodies were observed under cytochemical staining and transmission electron microscopy. FCM analysis showed hypodiploid peaks on histogram, the apoptotic rates at the concentrations of 50, 75, 100, 150 and 200 mg/L of HAP nanoparticles were 20.35+/-2.23 %, 25.35+/-1.92 %, 29.34+/-4.61 %, 44.92+/-3.78 % and 53.64+/-3.49 %, respectively, which were all significantly higher than that of control group 2.23+/-0.14 %. There was a significant correlation between HAP nanoparticle concentration and apoptotic rate (r=0.994, P<0.01). CONCLUSION: HAP nanoparticles not only inhibit proliferation but also induce apoptosis of human hepatoma cell line BEL-7402 in vitro.
AIM: To study the effect of hydroxyapatite (HAP) nanoparticles on humanhepatoma cell line BEL-7402 in vitro. METHODS: The humanhepatoma cell line BEL-7402 was cultured and treated with HAP nanoparticles at various concentrations. Growth suppression was detected with MTT colorimetric assay, cell apoptotic alterations were evaluated by cytochemical staining (Hoechst 33258), transmission electron microscopy (TEM), and flow cytometry (FCM). RESULTS: HAP nanoparticles inhibited the growth of hepatoma cells in a dose-dependent manner, with IC(50) values of 29.30 mg/L. Treated with 50-200 mg/L HAP nanoparticles for 48 h, BEL-7402 cells apoptosis with nuclear chromatin condensation and fragmentation as well as cell shrinkage and the formation of apoptotic bodies were observed under cytochemical staining and transmission electron microscopy. FCM analysis showed hypodiploid peaks on histogram, the apoptotic rates at the concentrations of 50, 75, 100, 150 and 200 mg/L of HAP nanoparticles were 20.35+/-2.23 %, 25.35+/-1.92 %, 29.34+/-4.61 %, 44.92+/-3.78 % and 53.64+/-3.49 %, respectively, which were all significantly higher than that of control group 2.23+/-0.14 %. There was a significant correlation between HAP nanoparticle concentration and apoptotic rate (r=0.994, P<0.01). CONCLUSION: HAP nanoparticles not only inhibit proliferation but also induce apoptosis of humanhepatoma cell line BEL-7402 in vitro.
Authors: Jennifer M Richards; Jennie A M R Kunitake; Heather B Hunt; Alexa N Wnorowski; Debra W Lin; Adele L Boskey; Eve Donnelly; Lara A Estroff; Jonathan T Butcher Journal: Acta Biomater Date: 2018-03-02 Impact factor: 8.947
Authors: Jedd M Hillegass; Arti Shukla; Sherrill A Lathrop; Maximilian B MacPherson; Naomi K Fukagawa; Brooke T Mossman Journal: Wiley Interdiscip Rev Nanomed Nanobiotechnol Date: 2010 May-Jun