Our teams worldwide are working to ensure uninterrupted availability of our products and services, and we continue to be fully operational during the COVID-19 outbreak. However, due to the uncertainty of this situation, we may not be able to answer the phone immediately. Here are some quick alternative ways to contact us.
Higher single-cell cloning efficiency The Cellartis iPSC Single-Cell Cloning DEF-CS Culture Media Kit better supports establishment of hiPS cell clones than competitors' culture systems.
Robust expansion of clones The Cellartis iPSC Single-Cell Cloning DEF-CS Culture Media Kit promotes robust proliferation of clonal hiPS cell colonies.
Pluripotency maintained after single-cell cloning Clones established and grown in the DEF-CS system maintain high expression levels of TRA-1-60 and SSEA-4, while clones established and grown using competitors' systems lose expression of these pluripotency markers.
Recent progress in gene editing technology has made it possible to introduce targeted genetic alterations in cells and organisms. These methods are being applied in human-induced electroporation stem (hiPS) cells, for functional studies of genetic variation in disease models and for the larger field of regenerative medicine; however, a major barrier remains at the level of selecting single cells with the desired mutations. Currently, it is difficult to treat isolated clonal cells in a manner that allows them to survive the gene editing procedure and thrive. This single-cell cloning bottleneck occurs because delicate hiPS cells typically grow in colony- and/or feeder-dependent conditions, and re-plating as single cells removes survival and growth signals, reducing viability. Promoting survival and proliferation at the single-cell level is critical for expansion of any clonal colonies containing the mutation of interest from the gene editing process.
Unfortunately, gene editing protocols often subject stem cells to harsh conditions that compromise their survival (e.g., electroporation), a problem that is compounded by the innate challenges of single-cell culture. A culture system that supports single-cell cloning and expansion of hiPS cells could overcome the current barrier of poor outcomes for single cells. This type of improved culture system should be feeder-free and defined, as the use of feeder cells results in a more complicated workflow, more labor, inaccurate quantification, and an increased risk of heterogeneous cultures.
Additionally, the ideal system should sustain a feeder-free hiPS cell monolayer culture while going through the gene editing technique of choice, and then further ensure survival and proliferation once single cells are plated and expanded for mutant allele identification. Monolayer culture systems and colony systems differ in the growth patterns of the hiPS cells they support; the former supports a sheet of cells and the latter multiple colonies.
The Cellartis iPSC Single-Cell Cloning DEF-CS Culture Media Kit, recognized for its suitability for genome engineering (Valton et al. 2014) and single-cell cloning (Feng et al. 2014), promotes reliable growth of hiPS cells in a feeder-free and defined environment. Cells are grown as a homogeneous monolayer and are enzymatically passaged as single cells that maintain pluripotency with a stable karyotype for more than 20 passages (Asplund et al. 2016). The same reagents are used for monolayer and single-cell culture, reducing variability. In the following experiments, we demonstrate that the Cellartis iPSC Single-Cell Cloning DEF-CS Culture Media Kit is ideal for single-cell culture. We also report a comparison between this system and two commercially available, feeder-free culture systems on their performance with single-cell cloning and expansion of cloned hiPS cells. Cloning efficiency measurements and pluripotency analysis indicate that the Cellartis iPSC Single-Cell Cloning DEF-CS Culture Media Kit is the most efficient system for single-cell cloning, supporting expansion of clones while maintaining pluripotency.
The Cellartis iPSC Single-Cell Cloning DEF-CS Culture Media Kit enables establishment of robust colonies after single-cell seeding
For gene editing experiments, edited cells can be passaged by serial dilution into single-cell culture conditions (or FACS sorted, one cell per well). Supporting survival and growth of "emerging clones" at this stage is critical for success; any colony loss could mean a loss of the desired mutant. Optimal performance of hiPS cell culture systems occurs when there is a high enough seeding density for the cells to support their growth through cell-cell contact signals and a sufficient concentration of secreted soluble factors. However, system performances may diverge as the seeding density decreases.
In order to determine the performances of the Cellartis system and the systems from Vendor 1 and Vendor 2 over a range of seeding densities, cells from Cellartis Human iPS Cell Line 18 (ChiPSC18, a delicate stem cell line) were diluted serially and seeded at concentrations ranging from ~0.5–450 cells/well into 96-well plates. After 9–11 days, wells with surviving cells were counted to determine the supportive capability of each system. While the Cellartis iPSC Single-Cell Cloning DEF-CS Culture Media Kit performed as well as or better than competitors' systems in the range of ~2–50 cells/well (the light yellow section of Figure 1, below), it showed a unique capability to support an initial seeding density of ≤1 cell/well (the dark yellow section). At a seeding density of one cell per well, the DEF-CS system was the only system that showed robust survival and proliferation of clones, indicating the suitability of the DEF-CS system for experiments that require single-cell survival.
Since the competitors' systems were unable to support viable colonies in the previous experiment using a delicate stem cell line, they were additionally tested with more robust cell lines: ChiPSC22 (known for its robustness) and ChiPSC12 (with more average features). In Figure 2, cells from ChiPSC12, ChiPSC18, or ChiPSC22 were grown in the DEF-CS system, Vendor 1's system, or Vendor 2's system (three cell lines x three culture systems = nine conditions total). After single-cell cloning in 96-well plates (as described in the Methods section), the growth of the emerging clones was observed by phase contrast microscopy, and the number of wells containing healthy-looking colonies was counted.
The Cellartis iPSC Single-Cell Cloning DEF-CS Culture Media Kit maintains pluripotency of cloned hiPS cells
For successful single-cell cloning, not only do the cells need to give rise to emerging clones (through healthy proliferation of the seeded single cells within the original wells), but the emerging clones also need to be pluripotent, robust, and expandable (able to maintain proliferative capacity after passaging into larger wells, or to be an "expandable colony"). The stability of hiPS cells as they are repeatedly dissociated, plated, and expanded is critical for successful gene editing; cells must maintain their original pluripotent identity, indicating their potential to be differentiated into cell types from all three germ layers. A solid indicator of stemness is the presence of pluripotency markers TRA-1-60 and SSEA-4.
Emerging clones from experiments 1 and 2 were passaged according to each culture system's manual and the established hiPS cell cultures were analyzed for protein expression of TRA-1-60 and SSEA-4. For cells grown in the DEF-CS system, 29 clones were analyzed (26% of the emerging clones). For cells grown in Vendor 1's system, 14 clones were analyzed (19% of the emerging clones), and for Vendor 2's system, 6 clones were analyzed (55% of the emerging clones). Flow cytometry analysis indicated that the clones established in the DEF-CS system maintained the highest proportion of TRA-1-60-positive, SSEA-4-positive, and double-positive cells, while the clones in the competitors' systems partially or completely lost the expression of these pluripotency markers. In Figure 3, the results from up to five representative colonies established and grown in the different culture systems are compared; each set of three bars shows data from one representative expandable colony derived from each viable emerging clone.
In order for single-cell cloning to be truly successful, a high efficiency in the number of seeded single cells that become emerging clones must be combined with a high capability of the emerging clones to be converted into expandable colonies—that is, established, undifferentiated hiPS cell lines. Emerging colonies must be able to be passaged separately, and after passage, >90% of the cells in each expandable colony must stain positive for TRA-1-60 and SSEA-4, representing high-quality hiPS cells. In the following analysis, data from ChiPSC12, ChiPSC22, and ChiPSC18 were averaged across the cell lines. For cells grown in the DEF-CS system (29 clones analyzed), 97% met the threshold of >90% TRA-1-60+/SSEA-4+ cells. For cells grown in Vendor 1's system (14 clones analyzed), only 7% met this threshold, and for cells grown in Vendor 2's system (6 clones analyzed), 33% met the threshold. Figure 4 shows the total percentage of seeded single cells that could be converted into undifferentiated lines. DEF-CS technology stands out as highly effective for the conversion of emerging clones into high-quality cell lines.
The Cellartis iPSC Single-Cell Cloning DEF-CS Culture Media Kit promotes robust clonal expansion
The ultimate goal for single-cell culture is to generate stable, healthy clonal cell populations that can be used for a variety of experiments. The DEF-CS system reaches this goal; it provides the ideal environment for single-cell survival and colony growth by fostering growing colonies, so they are fit for subsequent expansion, and by maintaining a pluripotent status throughout the process. In the time-lapse images below, a seeded single cell was grown using the DEF-CS system and followed over eight days to track its emergence into a healthy colony.
Results demonstrated that the Cellartis iPSC Single-Cell Cloning DEF-CS Culture Media Kit showed robust expansion ability in all three iPS cell lines, while the other systems failed in supporting the establishment and expansion of single cells (Figures 1, 2, and 3) and/or in maintaining pluripotency levels (Figures 3 and 4).
Gene editing of human induced pluripotent stem cells requires a culture system that can support single-cell culture, robust proliferation, expansion, and maintenance of pluripotency. The type of culture system should be considered: standard stem cell culture systems may perform differently with single-cell culture than those designed for monolayer culture. In this study, the performance of the Cellartis iPSC Single-Cell Cloning DEF-CS Culture Media Kit, a monolayer culture system, was compared with those of two commonly used colony culture systems from different vendors, using multiple cell lines. The data demonstrated that the DEF-CS system allowed efficient single-cell cloning and expansion of hiPS cells, and the established clones maintained their dual expression of TRA-1-60 and SSEA-4. Indeed, the other systems were not able to promote robust single-cell survival, proliferation, or expansion to the same degree as the DEF-CS system, and the clones in those systems completely or partially lost expression of the aforementioned pluripotency markers. The DEF-CS system proved superior for single-cell cloning, making it an ideal choice for advancing experiments that require sensitive handling of edited hiPS cells.
Cellartis Human iPS Cell Lines 12, 18, and 22 were cultured in the Cellartis iPSC Single-Cell Cloning DEF-CS Culture Media Kit and competitors' feeder-free culture systems (Vendors 1 and 2) for three weeks according to the manufacturers' protocols. Then, cells were enzymatically passaged (or equivalent) and seeded onto coated 96-well plates at ~0.5–450 cells/well for the experiment represented by Figure 1, and at 1 cell/well for the remaining figures. For the experiments represented by Figures 2, 3, and 4, expandable clones were created by passaging colonies (1:1) from the original 96-well plates into 48-well plates. The medium was changed every other day until analysis was performed between days 9 and 11.
Cloning efficiency and flow cytometry
After seeding, phase contrast microscopy was used to verify wells containing single cells. Wells containing multiple cells were eliminated from the calculation of single-cell cloning efficiency. Ten days after seeding, cell growth in 96-well plates was again observed by microscopy, the number of wells containing healthy-looking colonies was counted, and cloning efficiency was calculated. Single-cell cloning efficiency was expressed as a %; it was calculated by dividing the number of healthy-looking wells (emerging clones) by n (# of seeded wells) and multiplying by 100. For the experiments represented by Figures 3 and 4, healthy-looking colonies were passaged and further expanded. These clones were stained with TRA-1-60 and SSEA-4 antibodies conjugated to Alexa Fluor 488 and phycoerythrin, respectively. The cells were analyzed by flow cytometry, and the percentages of TRA-1-60-positive, SSEA-4-positive, and double-positive cells were quantified.
Asplund, A. et al. One Standardized Differentiation Procedure Robustly Generates Homogenous Hepatocyte Cultures Displaying Metabolic Diversity from a Large Panel of Human Pluripotent Stem Cells. Stem Cell Rev. Reports12, 90–104 (2016).
Feng, Q. et al. Scalable Generation of Universal Platelets from Human Induced Pluripotent Stem Cells. Stem Cell Reports3, 817–831 (2014).
Valton, J. et al. Efficient strategies for TALEN-mediated genome editing in mammalian cell lines. Methods69, 151–170 (2014).