The rapid development and continued evolution of iPS technology has sparked discussions about the need for establishing standards to guide the field.
As researchers seek new methods to create iPS cells without genetic modification and the use of these cells to develop disease models continues to expand rapidly, questions arise as to whether these cells have the same properties and potential as embryonic stem cells. How can a researcher know for certain that he or she has generated iPS cells? Is there a minimum set of criteria for assessing whether a somatic cell is fully pluripotent or only partially reprogrammed?
Adding to this complexity, researchers also seek to understand the variation between iPS cell lines derived from a common somatic source.
Dr. Clegg’s lab is looking at the similarities and differences between iPS cell lines derived from human fetal RPE cells. “The question we were trying to address,” describes Dr. Clegg, “is if we take those cells down to iPS cells and just let them spontaneously differentiate, will they have some sort of epigenetic memory and tend to re-differentiate back into RPE or something else?
“The first line we looked at snapped back in large quantities to RPE cells,” reports Dr. Clegg. “But each subsequent line we looked at was different. That’s an important lesson for people to understand—each iPS line that’s generated is slightly different, just like each embryonic stem cell line is slightly different. They have different propensities for differentiation. They may have different epigenetics. They may have different expression patterns.”
“We’re still learning to define what is the best iPS cell,” notes Dr. Cowan. “The best function identically to an embryonic stem cell. It remains pluripotent, expands, and self-renews and it can differentiate into the types of tissues you’re interested in.”
An article by Maherali and Hochedlinger (Cell Stem Cell Protocol Review, December 4, 2008) suggests a minimal set of criteria that should be fulfilled in order to ascertain that a genuine iPS cell has been generated. The criteria include:
- all morphological attributes including unlimited self-renewal;
- expression of key pluripotency genes with downregulation of lineage-specific genes associated with the cell of origin;
- transgene independence;
- proof of functional differentiation through the highest stringency test acceptable.
With human iPS cells, pluripotency can be assessed based on teratoma formation, which is a specific type of tumor containing cells from all three germ layers.
Researchers are also probing the similarity of iPS cell and embryonic cells through microarray studies, high-throughput sequencing, assessment of DNA methylation status at pluripotent cell specific genes, and by examining a range of protein biomarkers.
As our understanding of the similarities and differences between iPS cells and embryonic stem cells grows, new tools to identify and compare these cell types are needed. For example, live-cell imaging can be used to distinguish between human iPS cells and partially reprogrammed cells.
While standards provide a good basis of comparison, Dr. Cowan suggests that standards can be restrictive. “The standards are naturally evolving. We certainly need to maintain a minimum standard and recognize the standard will change over time. Within a year or two, there will probably be a new set of guidelines available. But there may be times when you may not want to make something that is an embryonic cell.
“In fact, it may be more to your advantage to somehow uniquely trap a cell so that it is lineage-committed to something that can replicate in culture indefinitely but really only thinks of itself as ‘lung,’ for example, and so would only ever differentiate back to lung cell types.”
While a great deal remains to be learned about iPS cells, they represent a powerful new research tool. In addition to their potential impact on the field of regenerative medicine, use of iPS cells to dissect complicated diseases at the cellular level will provide valuable new insights supporting drug discovery. As we learn more about the nature of iPS cells, standards will certainly evolve and new tools will become available to facilitate efficient creation and routine culture.