A comparison of DNA damage induced by aflatoxin B1 in hepatocyte-like cells, their progenitor mesenchymal stem cells and CD34+ cells isolated from umbilical cord blood
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作者:
Ghaderi, Masoumeh
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Tarbiat Modares Univ, Fac Med Sci, Dept Biochem, Tehran, IranTarbiat Modares Univ, Fac Med Sci, Dept Biochem, Tehran, Iran
Ghaderi, Masoumeh
[1
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Allameh, Abdolamir
[1
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Soleimani, Masoud
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Tarbiat Modares Univ, Fac Med Sci, Dept Hematol, Tehran, IranTarbiat Modares Univ, Fac Med Sci, Dept Biochem, Tehran, Iran
Soleimani, Masoud
[2
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Rastegar, Hossein
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Minist Hlth & Med Educ, Food & Drug Control Lab, Tehran, IranTarbiat Modares Univ, Fac Med Sci, Dept Biochem, Tehran, Iran
Rastegar, Hossein
[3
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Ahmadi-Ashtiani, Hamid Reza
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Tarbiat Modares Univ, Fac Med Sci, Dept Biochem, Tehran, IranTarbiat Modares Univ, Fac Med Sci, Dept Biochem, Tehran, Iran
Ahmadi-Ashtiani, Hamid Reza
[1
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机构:
[1] Tarbiat Modares Univ, Fac Med Sci, Dept Biochem, Tehran, Iran
[2] Tarbiat Modares Univ, Fac Med Sci, Dept Hematol, Tehran, Iran
[3] Minist Hlth & Med Educ, Food & Drug Control Lab, Tehran, Iran
This study compared the sensitivity of differentiated hepatocyte-like cells, their progenitor mesenchymal stem cells (MSCs) and CD34(+) stem cells to DNA damage and toxicity induced by aflatoxin B1 (AFB1). The hepatocyte-like cells and their progenitor cells (isolated from umbilical cord blood (UCB)) were each treated with AFB1 on day 15 of differentiation. Cell toxicity and genotoxicity effects were assessed using MTT and alkaline comet assays. AFB1 treatment resulted in a dose- and time-dependent inhibition of cell growth. The IC50 values of AFB1 for hepatocytes differentiated from CD34(+) and MSCs were within the same range (44.7-46.8 mu M). The IC50 calculated for non-differentiated MSCs and CD34(+) cells was slightly lower (42.0-43.4 mu M) than that calculated for their differentiated counterparts. However, the extent of DNA damage was different in differentiated and non-differentiated cells. The percentages of DNA (% DNA) in comet tails measured in hepatocytes differentiated from MSCs exposed to AFB1 (0, 2.5, 10 and 20 mu M) for 24h were similar to 15, 55,65 and 70%, respectively. In comparison, hepatocytes from CD34(+) cells were more resistant to AFB1-induced DNA damage. Hepatocyte-MSCs were most sensitive to DNA damage, followed by UCB-CD34(+) cells, then UCB-MSCs and finally hepatocyte-CD34(+) cells. These results clearly showed that stem cells from different sources have different sensitivities to DNA damaging agents. These differences can be assigned to the expression levels of cytochrome P450 (CYP) particularly CYP3A4 in non-differentiated and differentiated cells. These data are useful in better understanding the susceptibility/resistance of stem cells in the process of differentiation to environmental toxicants. (C) 2010 Elsevier B.V. All rights reserved.
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Newcastle Univ, Fac Med Sci, Sch Clin & Lab Sci, Newcastle Upon Tyne, Tyne & Wear, EnglandNewcastle Univ, Fac Med Sci, Sch Clin & Lab Sci, Newcastle Upon Tyne, Tyne & Wear, England
Lu, Xiaomei
Forraz, Nico
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Newcastle Univ, Fac Med Sci, Sch Clin & Lab Sci, Newcastle Upon Tyne, Tyne & Wear, EnglandNewcastle Univ, Fac Med Sci, Sch Clin & Lab Sci, Newcastle Upon Tyne, Tyne & Wear, England
Forraz, Nico
McGuckin, Colin P.
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Newcastle Univ, Fac Med Sci, Sch Clin & Lab Sci, Newcastle Upon Tyne, Tyne & Wear, EnglandNewcastle Univ, Fac Med Sci, Sch Clin & Lab Sci, Newcastle Upon Tyne, Tyne & Wear, England
McGuckin, Colin P.
Dickinson, Anne M.
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Newcastle Univ, Fac Med Sci, Sch Clin & Lab Sci, Newcastle Upon Tyne, Tyne & Wear, EnglandNewcastle Univ, Fac Med Sci, Sch Clin & Lab Sci, Newcastle Upon Tyne, Tyne & Wear, England
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Fourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R ChinaFourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R China
Zhou, Xia
Cui, Lina
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Fourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R ChinaFourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R China
Cui, Lina
Zhou, Xinmin
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Fourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R ChinaFourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R China
Zhou, Xinmin
Yang, Qiong
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Fourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R ChinaFourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R China
Yang, Qiong
Wang, Lu
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Fourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R ChinaFourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R China
Wang, Lu
Guo, Guanya
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Fourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R ChinaFourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R China
Guo, Guanya
Hou, Yu
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Fourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R ChinaFourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R China
Hou, Yu
Cai, Weile
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Fourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R ChinaFourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R China
Cai, Weile
Han, Zheyi
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Fourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R ChinaFourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R China
Han, Zheyi
Shi, Yongquan
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Fourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R ChinaFourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R China
Shi, Yongquan
Han, Ying
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Fourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R ChinaFourth Mil Med Univ, State Key Lab Canc Biol, Xijing Hosp Digest Dis, Xian, Shaanxi, Peoples R China