Germline transmission of an embryonic stem cell line derived from BALB/c cataract mice

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Abstract

Mice embryonic stem (ES) cells have enabled the generation of mouse strains with defined mutation(s) in their genome for putative disease loci analysis. In the study of cataract, the complex genetic background of this disease and lack of long-term self-renewal ES cells have hampered the functional researches of cataract-related genes. In this study, we aimed to establish ES cells from inherited cataract mice (BALB/CCat/Cat). Embryos of cataract mice were cultured in chemical-defined N2B27 medium with the presence of two small molecules PD0325901 and CHIR99021 (2i) and an ES cell line (named EH-BES) was successfully established. EH-BES showed long-term self-renewal in 2i medium and maintained capacity of germline transmission. Most importantly, the produced chimera and offspring developed congenital cataract as well. Flow cytometry assay revealed that EH-BES are homogeneous in expression of Oct4 and Rex1in 2i medium, which may account for their selfrenewal ability. With long-term self-renewal ability and germline-competent, EH-BES cell line can facilitate genetic and functional researches of cataract-related genes and better address mechanisms of cataract. ©Peng et al.

Figures

  • Figure 1. Establishment of EH-BES cell line in 2i medium. (A) Embryos from BALB/CCat/Cat mice were separately seeded in 2i medium on gelatin-coated plastics and ES cells-like colony emerged in 3 days. (B) EH-BES cell line was established and maintained with or without feeders. (C) EHBES cells were AP-staining positive (left); EH-BES cells showed Nanog-expression by immunostaining analysis (right). (D) EH-BES cells showed Oct4expression. (E) EH-BES cells showed Sox2-expression. DAPI stain indicates nuclei in blue. Scale bars stand for 100 mm. doi:10.1371/journal.pone.0090707.g001
  • Figure 3. EH-BES had normal karyotype and produced chimeras. (A) EH-BES had normal karyotype (40 chromosomes). (B) The female chimera showed chimeric coat color and cataract development (indicated by arrow). (C) The female chimera (indicated by arrow) produced four offspring after mated with normal BALB/C mouse, of which two offspring showed white coat color. (D) The white offspring showed cataract development (indicated by arrow). doi:10.1371/journal.pone.0090707.g003
  • Figure 4. After 2 passages, EH-BES cells exhibited different morphology in different culture medium. (A) EH-BES cells differentiated in N2B27 medium. (B) EH-BES cells cultured in serum medium were heterogeneous in morphology. (C) EH-BES formed tightly-packed undifferentiated colonies in 2i medium. (D) Cells in N2B27 medium were Oct4-negative by flow cytometry assay (left); cells in serum medium were heterogeneous in expression of Oct4 (middle); cells in 2i medium were homogenous in Oct4-expression (right). (E) Cells in 2i medium showed significantly higher percentage of Oct4-positive cells compared with those in serum medium (* indicates p,0.001). (F) EH-BES cells totally lost Rex1-expression in N2B27 medium (left); EH-BES cells were heterogeneous in Rex1-expression in serum medium (middle); EH-BES cells were rather homogeneous in Rex1expression in 2i medium (right). (G) EH-BES cells in 2i medium showed significantly higher percentage of Rex1-positive cells compared with those in serum medium (* indicates p,0.001). Scale bars stand for 100mm. doi:10.1371/journal.pone.0090707.g004

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APA

Peng, X., Liu, T., Shi, C., Zhang, L., Wang, Y., Zhao, W., … Qian, Q. (2014). Germline transmission of an embryonic stem cell line derived from BALB/c cataract mice. PLoS ONE, 9(3). https://doi.org/10.1371/journal.pone.0090707

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