- Open Access
Efficient production of chimeric mice from embryonic stem cells injected into 4- to 8-cell and blastocyst embryos
© Hu et al.; licensee BioMed Central Ltd. 2013
- Received: 17 December 2012
- Accepted: 15 March 2013
- Published: 21 March 2013
Production of chimeric mice is a useful tool for the elucidation of gene function. After successful isolation of embryonic stem (ES) cell lines, there are many methods for producing chimeras, including co-culture with the embryos, microinjection of the ES cells into pre-implantation embryos, and use of tetraploid embryos to generate the full ES-derived transgenic mice. Here, we aimed to generate the transgenic ES cell line, compare the production efficiency of chimeric mice and its proportion to yield the male chimeric mice by microinjected ES cells into 4- to 8-cell and blastocysts embryos with the application of Piezo-Micromanipulator (PMM), and trace the fate of the injected ES cells.
We successfully generated a transgenic ES cell line and proved that this cell line still maintained pluripotency. Although we achieved a satisfactory chimeric mice rate, there was no significant difference in the production of chimeric mice using the two different methods, but the proportion of the male chimeric mice in the 4- to 8-cell group was higher than in the blastocyst group. We also found that there was no tendency for ES cells to aggregate into the inner cell mass using in vitro culture of the chimeric embryos, indicating that they aggregated randomly.
These results showed that the PMM method is a convenient way to generate chimeric mice and microinjection of ES cells into 4- to 8-cell embryos can increase the chance of yielding male chimeras compared to the blastocyst injection. These results provide useful data in transgenic research mediated by ES cells.
- Chimeric mice
- Embryonic stem cell
Embryonic stem (ES) cells derived from the inner cell mass (ICM) of blastocysts can maintain their self-renewal during in vitro culture and have the amazing ability of developing into all three germ layers, including germ cells . The ES cells can be genetically manipulated in vitro by introducing targeted mutations and other genetic alterations into the mice genome, providing a powerful tool for understanding gene function in vivo[1–7] and contributing significantly to biomedical research [8, 9]. Due to the powerful function of ES cells, chimeras have become important tools for the study of cell lineage differentiation and embryogenesis. In 1961, the first chimeric mice were generated by aggregation of two 8-cell stage embryos . Since then, different methods of producing chimeric mice and more efficient equipment have been created. Until now, the production of chimeras by microinjected genetically modified ES cells into blastocysts or zygotes [11, 12] or 8-cell stage embryos  was successful. In addition, chimeric mice can also be produced by aggregation of ES cells with cleavage embryos [14–16]. The Piezo-Micromanipulator (PMM) method, which originally was successfully used for intracytoplasmic sperm injection (ICSI) and somatic cell cloning [17, 18], was also used in chimeric mice production . Laser-assistance of injecting ES cells into 8-cell stage embryos could more efficiently produce F0 ES mice with full germ-line transmission compared to the tetraploid complementation method . Recently, Huang report that injection of ES cells into 4- or 8-cell embryos with the application of PMM could directly produce the F0 ES cell offspring .
In the present study, we generated an EGFP-ES cell line and tested the efficiency of producing chimeric mice by injecting the ES cells into 4- to 8-cell and blastocyst embryos with the application of PMM. The proportion of male chimeric mice and in vitro development of the chimeric embryos was also analyzed.
Embryos and recipient mice
All animal procedures were performed according to guidelines developed by the China Council on Animal Care and protocols were approved by the Animal Care and Use Committee of Guangdong Province, China. The approval ID or permit numbers are SCXK (Guangdong) 2004–0011 and SYXK (Guangdong) 2007–0081.
CD-1 females were superovulated by intraperitoneal injection of 5 IU pregnant mare serum gonadotrophin followed by 5 IU human chorionic gonadotrophin (HCG) 46 to 48 h later. After the HCG injection, these female mice were mated with male mice of the same strain. Females were screened for vaginal plugs the following morning (0.5 d post coitum, [dpc]), and fertilized embryos were collected and cultured in potassium simplex optimization medium (KSOM), overlaid with embryo-tested mineral oil in humidified atmospheres of 5% CO2 at 37°C. CD-1 females were mated with vasectomized CD-1 males and used as recipients for embryo transfer at 0.5 or 2.5 dpc. Unless otherwise specified, all reagents were obtained from Sigma-Aldrich.
Transgenic ES cell line and culture
We used the R1 ES cell line, routinely cultured on inactivated cellular feeder layers in ES cell medium, composed of Dulbecco’s modified Eagle’s medium (Gibco), supplemented with 20% fetal bovine serum (Gibco), 1% nonessential amino acid (Gibco), 0.1 mmol/L β-mercaptoethanol (Gibco), 1 mmol/L glutamine (Gibco), 1% nucleosides (Gibco), 50 units/mL penicillin, 50 μg/mL streptomycin (Gibco) and 1,000 units/mL recombinant mice leukemia inhibitory factor (Millipore). ES cells were electroporated with the linearized pEGFP-N1 (Clontech) by using a BTX Electroporation Generator (BTX, Inc., San Diego, CA) at 250 V and 90 μs. Neomycin (Gibco) selection was performed 2 d after transfection to obtain stable transgenic ES cell lines.
Characterization of transgenic ES cell line
Immunohistochemistry and AP staining
ES cells grown on feeder cells were fixed in 4% paraformaldehyde for 20 min, permeabilized with 0.2% Triton X-100 for 30 min, and blocked in 3% bovine serum albumin in phosphate-buffered saline (PBS) for 2 h. Cells were incubated with primary antibody overnight at 4°C, washed, and incubated with Alexa Fluor (Invitrogen) secondary antibody for 3 h. Oct4 and Sox-2 antibodies were obtained from Millipore. Alkaline phosphatase staining was done according to the manufacturer’s recommendations (Millipore).
ES cells were washed with PBS, trypsinized to obtain a single-cell suspension, and collected by centrifugation. 2×106 cells were subcutaneously injected into immune-deficient BALB/cA-nu mice. 4 wk after injection, teratomas were dissected, rinsed once with PBS, and fixed in 10% formalin. Teratomas were embedded in paraffin, sectioned, stained with hematoxylin/eosin, and then visualized with a Olympus(IX71) microscope and photographed.
Expression analysis of pluripotency marker genes by RT-PCR
Primers used for detection of pluripotency marker genes
CTG AGG GCC AGG CAG GAG CAC GAG
CTG TAG GGA GGG CTT CGG GCA CTT
AGG GTC TGC TAC TGA GAT GCT
CAA CAC CTG GTT TTT CTG CCA CCG
GGT TAC CTC TTC CTC CCA CTC CAG
TCA CAT GTG CGA CAG GGG CAG
ACG AGT GGC AGT TTC TTC TTG GGA
TAT GAC TCA CTT CCA GGG GGC ACT
CCG CCA CCA GTT CGC CAT G
CCG CTC GTT GCC AAT AGT GAT GAC
In vitro formation of embryoid body
ES cells were washed with PBS, trypsinized, resuspended with embryoid body (EB) medium (without LIF), and 20- to 30-μL drops containing 400 to 1,000 ES cells were plated on the lid of petri dishes in regular arrays. A 100-mm dish can accommodate approximately 30 to 40 drops. The lid was inverted and placed over the bottom of a petri dish filled with PBS to prevent the drops from drying out. The petri dishes with hanging drops were incubated for 2 d. Embryoid body-like aggregates were harvested and subsequently transferred into bacterial-grade dishes and cultivated for 3 to 5 d. For further differentiation, 5 to 7-d-old EBs were plated on gelatin-coated tissue culture plates.
The ES cells were injected into the mice embryos by PMM as described [17–19]. Fertilized embryos were cultured in KSOM in vitro until 2.0 dpc, 2.5 dpc, and 3.5 dpc for the production of 4- to 8-cell and blastocyst embryos. ES cells were trypsinized to obtain a single-cell suspension, and the cell suspension was kept on ice in 1 mL ES cell medium with HEPES in a 15-mL tube until use. Ten to fifteen ES cells were injected into the 4- and 8-cell and blastocyst embryos, injected blastocysts were cultured in KSOM at 37°C in an atmosphere of 5% CO2 for 1 to 2 h until the blastocyst cavity was recovered.
Healthy microinjected 4- to 8-cell embryos were surgically transferred to the oviduct of 0.5 dpc pseudopregnant female recipients. The microinjected blastocysts were transferred to the uterine horns of 2.5 dpc pseudopregnant females using the standard procedure.
In vitro development of 4-cell stage embryos injected with ES cells were observed with an Olympus inverted fluorescence microscope until the blastocysts hatched.
In the efficiency of chimera production experiment, the data was processed with SPSS 17.0 (SPSS Inc., Chicago, IL) statistical software. Significance was declared at P≤0.05.
Production of transgenic ES cell line
Characterization of transgenic ES cell line
Generation of chimeric embryos and mice
Efficiency in the production of chimeras from ES cells injected into 4- to 8-cell and blastocyst stage embryos
No. injected embryos transferred
No. recipient mice
No. total born (%)
No. total chimeras (%)
No. total male (%)
4- to 8- cell
Studies on the control of gene expression in eukaryotes based on the ability to induce the transient and stable expression in mammalian cells have contributed greatly to our current knowledge of the molecular mechanisms governing regulation of gene expression. An individual gene proved to be repaired using homologous recombination in ES cells  and the first genetically engineered mutant mouse was generated in 1990 [3, 24] after the successful isolation of ES cell line. To date, various transfection methods have been developed to transfer particles into cells including calcium phosphate DNA precipitates , viral vectors , liposomes  and direct injection of genes into the nucleus. However, use of these methods is limited because: (1) they work efficiently in only limited cell types and most are adherent cells; and (2) cells transfected with these methods are subject to a high frequency of damage. Subsequently, a physical method that induces an enormous enhancement of DNA transport across cellular membranes was reported [28, 29]. Briefly, using the short electric impulses above a certain field, the membrane structure was permeable and it was convenient for the material to cross without damaging it. In addition, these methods were also used in embryo fusion. We also compared electroporation and liposome-mediated transfection, and found that not only the transfection efficiency but also the quality of the positive clones was superior after electroporation versus liposomes.
Various techniques have been developed to maintain the developmental potential of ES cells in vitro and restrict the developmental potential of host embryos to increase the efficiency of germline chimeric mice production [31, 32]. Tetraploid complement was the most efficient method to generate viable and fertile ES mice completely from ES cells  and it's the “gold standard” to test pluripotency of the cell lines. Unfortunately, tetraploid embryos are less viable than normal embryos; mice produced by this method have nonspecific lethality and congenital abnormalities and complications in phenotypic analysis . Previous observations showed that injection of ES cells at an earlier stage might increase degrees of ES cell contribution , and high viable germline chimeras were obtained by 8-cell embryo injection . With the application of laser and PMM, F0 ES mice with full germline transmission were generated successfully .
In the present study, we aimed to compare the efficiency of chimeric mice production with the PMM method by injecting high passage (over 35) ES cells into the 4- to 8-cell and blastocysts embryos. Our results showed that the efficiency of chimeras did not differ between the two types of embryo injection, but all were higher than previously reported . In 8-cell injection, the efficiency of chimera production and the proportion of male mice was much lower than previously reported . We were unable to yield the F0 mice based on 100% coat color, which was not consistent with previous reports [13, 20, 21]. We traced the fate of ES cells in chimeric embryos and found that ES cells did not preferentially allocate to the ICM. This was in accordance with the data on chimera production. Reports showed that the combination of the genotypes of ES cells and host blastocysts is important for production of germline transmission chimeras, and the C57BL/6 are the suitable host for 129-derived ES cells [3, 34]. In this study, ES cells were derived from 129 mice and had been cultured in vitro for a long time (over 35 passages). Although they retained their pluripotency, they might not be suitable for generating chimeras. Wang report that R1 cells lost their totipotency in producing viable ES mice after passage 14 and the CD-1 host embryos may have been unsatisfactory with the combination of ES cells .
In the present study, we successfully generated a transgenic ES cell line and we gained satisfactory efficiency of chimera production by injecting into 4- to 8-cell and blastocyst embryos with the PMM method, but we found no significant difference between the two types of injection. The injected ES cells had no tendency to integrate into the ICM of the embryos based on tracing the ES cell fate. Interestingly, we yielded a higher proportion of male chimeras by injecting ES cells into 4- to 8-cell stage embryos than blastocyst injection. In addition, the PMM method is an efficient way to generate chimeric mice. These results show that these methods provide another approach to developing transgenic mice derived from ES cells.
We thank Dr. Shaorong Gao for kindly providing the R1 ES cell line for these experiments.
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