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Neural Differentiation of Mouse Embryonic Stem Cells in Serum-free Monolayer Culture
Published on: May 14, 2015
Strain difference in establishment of mouse embryonic stem (ES) cell lines
E Kawase1, H Suemori, N Takahashi
1Division of Developmental Biology, Meiji Institute of Health Science, Odawara, Japan.
The International Journal of Developmental Biology
|June 1, 1994
Summary
Researchers successfully established mouse embryonic stem (ES) cell lines from diverse mouse strains, including C57BL/6 and BALB/c. These new ES cell lines show strain-specific characteristics but can produce chimeric mice and contribute to germ-line transmission.
Area of Science:
- Developmental Biology
- Genetics
- Stem Cell Biology
Background:
- Mouse embryonic stem (ES) cells are crucial for genetic manipulation.
- Current ES cell lines are predominantly derived from the 129/Sv strain.
- There is a need for ES cell lines from diverse inbred and mutant mouse strains.
Purpose of the Study:
- To establish efficient methods for deriving ES cell lines from various mouse strains.
- To characterize the properties of newly established ES cell lines.
- To assess the potential of these ES cell lines for genetic applications.
Main Methods:
- Utilized fibroblast cell line SL10 as feeder cells.
- Supplemented culture medium with 5,000 unit/ml LIF.
- Adapted ES cell culture and establishment procedures for different mouse strains.
Main Results:
- Successfully established ES cell lines from C57BL/6, BALB/c, BXSB/MpJ-Yaa, and MRL/Mp-lpr/lpr strains.
- Demonstrated strain-specific differences in ES cell establishment and culture.
- Confirmed normal karyotype and chimera production in most derived cell lines.
- Showcased germ-line contribution from several C57BL/6 ES cell lines.
Conclusions:
- ES cell lines can be generated from a variety of mouse strains.
- Strain-specific modifications are necessary for efficient ES cell derivation.
- The established ES cell lines possess functional characteristics for genetic studies and applications.

