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1.
Stem Cell Res ; 34: 101364, 2019 01.
Article in English | MEDLINE | ID: mdl-30611019

ABSTRACT

Although investigation with human embryonic stem cells (HESC) is not decreasing, the derivation of new lines has been diminished. The preeminence of only a few HESC lines in research is accompanied by lack of universal applicability of results as well as by genetic under-representation. We previously reported the derivation of one line with male karyotype from Mexican population. Here, we derived one HESC line (Amicqui-2) with female karyotype from poor-quality embryos. These line comply the pluripotent requirements (normal karyotype, detection of pluripotency-associated markers, mycoplasma test and teratoma formation) and could be a valuable model for studying diseases specific to under-represented population.


Subject(s)
Cell Culture Techniques/methods , Embryo, Mammalian/cytology , Human Embryonic Stem Cells/cytology , Animals , Cell Line , Female , Humans , Mexico , Mice
2.
Stem Cell Res ; 15(2): 322-4, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26246271

ABSTRACT

Data from the literature suggest that human embryonic stem cell (hESC) lines used in research do not genetically represent all human populations. The derivation of hESC through conventional methods involve the destruction of viable human embryos, as well the use of mouse embryonic fibroblasts as a feeder layer, which has several drawbacks. We obtained the hESC line (Amicqui-1) from poor-quality (PQ) embryos derived and maintained on human amniotic epithelial cells (hAEC). This line displays a battery of markers of pluripotency and we demonstrated the capacity of these cells to produce derivates of the three germ layers.


Subject(s)
Amnion/cytology , Embryo Culture Techniques/methods , Epithelial Cells/cytology , Human Embryonic Stem Cells/cytology , Cell Differentiation , Cells, Cultured , Embryo, Mammalian/cytology , Epithelial Cells/metabolism , Feeder Cells/cytology , Human Embryonic Stem Cells/metabolism , Humans , Karyotyping , Transcription Factors/genetics , Transcription Factors/metabolism
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