Background Mono-（2-ethylhexyl） phthalate （MEHP）, the metabolite of di-（2-ethylhexyl） phthalate （DEHP）, was suspected to be toxic to human embryos. This study contributes to investigating its toxic effects by a...Background Mono-（2-ethylhexyl） phthalate （MEHP）, the metabolite of di-（2-ethylhexyl） phthalate （DEHP）, was suspected to be toxic to human embryos. This study contributes to investigating its toxic effects by an embryonic stem cell test （EST） based on two human embryonic stem cell （hESCs） lines. Methods CH1 established in our own lab and H1, a federally registered cell line were two human embryonic stem cell lines used in this test. Four endpoint measurements were performed consisting of cell viability, proliferation ability, apoptosis as well as changes of gene expression patterns after spontaneous differentiation were determined. For measuring effects on the first three endpoints, the cells were treated with various concentrations of MEHP dissolved in dimethyl sulfoxide （DMSO） and only with DMSO which served as control and harvested after 5 days. For measuring effects during spontaneous differentiation, the RNA of embryoid bodies （EBs） formed after 8 days＇ MEHP exposure was collected and changes in differentiation specific gene expression patterns were analyzed by quantitative real time RT-PCR. Results As a result the viability and proliferation ability of both cell lines decreased significantly at 1000 μmol/L MEHP, while there was no effect on apoptosis or cell morphology. In addition MEHP also changed the gene expression pattern in the EBs of both cell lines. Conclusion MEHP in a high dose was cytotoxic and affected the development of hESCs, which indicates its embryo toxicitv in human embrvos.展开更多
基金This study was supported by Beijing Natural Science Foundation （No. 7112141）.
文摘Background Mono-（2-ethylhexyl） phthalate （MEHP）, the metabolite of di-（2-ethylhexyl） phthalate （DEHP）, was suspected to be toxic to human embryos. This study contributes to investigating its toxic effects by an embryonic stem cell test （EST） based on two human embryonic stem cell （hESCs） lines. Methods CH1 established in our own lab and H1, a federally registered cell line were two human embryonic stem cell lines used in this test. Four endpoint measurements were performed consisting of cell viability, proliferation ability, apoptosis as well as changes of gene expression patterns after spontaneous differentiation were determined. For measuring effects on the first three endpoints, the cells were treated with various concentrations of MEHP dissolved in dimethyl sulfoxide （DMSO） and only with DMSO which served as control and harvested after 5 days. For measuring effects during spontaneous differentiation, the RNA of embryoid bodies （EBs） formed after 8 days＇ MEHP exposure was collected and changes in differentiation specific gene expression patterns were analyzed by quantitative real time RT-PCR. Results As a result the viability and proliferation ability of both cell lines decreased significantly at 1000 μmol/L MEHP, while there was no effect on apoptosis or cell morphology. In addition MEHP also changed the gene expression pattern in the EBs of both cell lines. Conclusion MEHP in a high dose was cytotoxic and affected the development of hESCs, which indicates its embryo toxicitv in human embrvos.
