کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5861076 1562711 2016 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
ROS-dependent HMGA2 upregulation mediates Cd-induced proliferation in MRC-5 cells
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
پیش نمایش صفحه اول مقاله
ROS-dependent HMGA2 upregulation mediates Cd-induced proliferation in MRC-5 cells
چکیده انگلیسی


- HMGA2 plays an important role in Cd-induced cell cycle disorder and proliferation in MRC-5 cells.
- ROS formation might be a prerequisite for Cd-induced HMGA2 upregulation.
- HMGA2 might be an important biomarker in Cd-induced cell proliferation and other toxicities

Cadmium (Cd) is a heavy metal widely found in a number of environmental matrices, and the exposure to Cd is increasing nowadays. In this study, the role of high mobility group A2 (HMGA2) in Cd-induced proliferation was investigated in MRC-5 cells. Exposure to Cd (2 μM) for 48 h significantly enhanced the growth of MRC-5 cells, increased reactive oxygen species (ROS) production, and induced both mRNA and protein expression of HMGA2. Evidence for Cd-induced reduction of the number of G0/G1 phase cells and an increase in the number of cells in S phase and G2/M phase was sought by flow cytometric analysis. Western blot analysis showed that cyclin D1, cyclin B1, and cyclin E were upregulated in Cd-treated cells. Further study revealed that N-acetyl cysteine (NAC) markedly prevented Cd-induced proliferation of MRC-5 cells, ROS generation, and the increasing protein level of HMGA2. Silencing of HMGA2 gene by siRNA blocked Cd-induced cyclin D1, cyclin B1, and cyclin E expression and reduction of the number of G0/G1 phase cells. Combining, our data showed that Cd-induced ROS formation provoked HMGA2 upregulation, caused cell cycle changes, and led to cell proliferation. This suggests that HMGA2 might be an important biomarker in Cd-induced cell proliferation.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicology in Vitro - Volume 34, August 2016, Pages 146-152
نویسندگان
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