JAX GM faculty member Bill Skarnes. Photo by Cloe Poisson
Bill Skarnes and team established and characterized a stable iPSC line, KOLF2.1J, to act as a high-quality baseline platform for modeling human disease. This line is part of the catalog of human iPSCs at JAX.
About 15 years ago, researchers discovered a way to take an adult non-reproductive (somatic) cell and return it to a pluripotent or undifferentiated state. For example, a cell that was once part of the skin can be reverted to pluripotency. With the qualities that once made it part of the skin removed, the cell has the capacity to differentiate and divide into a variety of different cell and tissue types. This kind of cell, named induced pluripotent stem cells (iPSCs), give researchers a powerful tool to accurately model human disease.
Cell line complications
iPSC lines have become essential for determining the underlying genetic drivers of human disease. Genomes of iPSCs can be easily edited using the bacteria-based CRISPR/Cas9 technology to introduce or correct disease-associated variants. By focusing on one gene variation at a time, results of experiments have a clear genetic cause and effect to be easily compared to previous data. What poses a challenge for accurate disease modeling is the inherent variation between iPSC lines, as well as the wide variety of cell lines used in research between institutions, creating unwanted obstacles in data interpretation.
A stable iPSC cell line
Jackson Laboratory (JAX) Professor of Cellular Engineering Bill Skarnes, Ph.D., and colleagues have developed a cell line to address the challenges facing cellular modeling of disease. A paper published in Cell Stem Cell, “A reference human induced pluripotent stem cell line for large-scale collaborative studies” details how Skarnes and his team deeply characterized genetic properties of eight iPSC lines, with one rising above the rest. The cell line KOLF2.1J proved to be an all-around well-performing iPSC line with high genomic stability in post-edited clones. Meeting all the criteria for cellular engineering research, KOLF2.1J can act as a stable foundation for modeling hundreds of genetic alterations relevant to Alzheimer’s disease, rare disease, cancer, and more.
Team science
Through the partnership between the iPSC Neurodegenerative Disease Initiative and the Chan Zuckerberg Initiative, KOLF2.1J is available as both a reference parental line and with selected single nucleotide variants (SNVs) as part of the catalog of human iPSCs at JAX. The efforts of Skarnes and his team to meet the need for a common, well-characterized iPSC line will soon benefit research around the globe. By selecting KOLF2.1J as a cell line of choice, researchers will be able to generate consistent, integratable data and help accelerate human disease research. In collaboration with UConn Health, Skarnes and fellow JAX researchers are now planning to derive additional similarly well-characterized iPSC lines from healthy individuals of diverse genetic backgrounds.