Chemical Research in Chinese Universities ›› 2012, Vol. 28 ›› Issue (2): 276-281 .

• Articles • Previous Articles     Next Articles

Cytotoxicity and DNA Damage Effect of TGA-capped CdTe Quantum Dots

LI Yan-bo1, ZHANG Hai-xia1,2, GUO Cai-xia1, HU Gui-qin3, DU Hai-ying3, JIN Ming-hua3, HUANG Pei-li1, SUN Zhi-wei1,3, YANG Wen-sheng4   

  1. 1. School of Public Health and Family Medicine, Capital Medical University, Beijing 100069, P. R. China;
    2. Public Health Institute, Beijing Chaoyang District Centre for Disease Control and Prevention, Beijing 100021, P. R. China;
    3. School of Public Health, Jilin University, Changchun 130021, P. R. China;
    4. Key Laboratory of Surface and Interface Chemistry of Jilin Province, College of Chemistry, Jilin University, Changchun 130012, P. R. China
  • Received:2011-07-11 Revised:2011-11-02 Online:2012-03-25 Published:2012-03-08
  • Supported by:

    Supported by the Funding Project for Academic Human Resources Development in Higher Learning Institution Under the Jurisdiction of Beijing Municipality, China(No.PHR201006110) and the Innovative Team Project of Beijing Education Committee, China(No.PHR201107116).

Abstract: The cytotoxicity and DNA damage caused by thioglycolic acid(TGA)-capped cadmium telluride(CdTe) quantum dots(QDs) to hepatocyte line HL-7702 were investigated. Cell viability was measured by 3-(4,5-dimethyl- thiazol-2-yl)-2,5-diphenyltetrazolium bromide(MTT) assay; DNA damage was detected by single cell gel electro-phoresis(SCGE); the change of cell cycle progression was examined by propidium iodide(PI)-flow cytometry(FCM); apoptosis was measured by acridine orange/ethidium bromide(AO/EB) assay and Annexin V-FITC/PI-FCM(FITC: fluorescein isothiocyanate). The results show that the cytotoxicity induced by CdTe QDs was increased in a dose-dependent and time-dependent manner; after exposure to QDs for 24 h, as the exposure dose increased, the rate of DNA damage was significantly increased(P<0.05), and the degree of DNA damage was elevated. As the dose of CdTe QDs increased, the percentage of G0/G1 phase cells was significantly decreased(P<0.001), while the percent- tages of S and G2/M phases cells were significantly increased(P<0.001). In AO/EB assay, apoptotic cells could be observed under a fluorescence microscope, and apoptotic rate was increased as exposure dose increased. In Annexin V-FITC/PI-FCM assay, the apoptotic rates of CdTe QDs treated groups were significantly increased compared with that of control group(P<0.05). Our studies indicate that CdTe QDs could influence cell viability, and induce DNA damage, the S and G2/M phases arrest and apoptosis of HL-7702.

Key words: Apoptosis, CdTe quantum dot(QD), Cell cycle, Cell viability, DNA damage