You are hereFebruary 21, 2018
Building better tiny kidneys to test drugs and help people avoid dialysis
A free online kidney atlas built by University of Southern California (USC) researchers empowers stem cell scientists everywhere to generate more human-like tiny kidneys for testing new drugs and creating renal replacement therapies.
"Stem-cell based technologies hold great promise for developing kidney replacement and regeneration therapies," said Nils Lindstrom, Ph.D., first author of three new studies and a research associate in Stem Cell Biology and Regenerative Medicine at USC’s Keck School of Medicine. "Getting there requires detailed knowledge of how kidneys normally form so the process can be replicated in cell cultures in the lab. Our data will help us and other scientists improve current techniques to make better tiny functional kidneys."
Over the past four years, USC Stem Cell researchers and USC Viterbi School of Engineering computer scientists have documented the molecular, cellular and genetic similarities and differences between human and mouse kidney formation so they can find treatments for kidney disease, which affects about 30 million Americans.
The three-study series, published on Feb. 15 in the Journal of the American Society of Nephrology, provides the first cellular and molecular characterization of how the human kidney develops in a mother's womb, said Andrew McMahon, Ph.D., study senior author and a professor at the Keck School of Medicine.
Kidney research has been a focus of the McMahon Lab for the past quarter century.
"Our research bridges a critical gap between animal models and human applications," Dr. McMahon said. "The data we collected and analyzed creates a knowledge base that will accelerate stem cell-based technologies to produce mini-kidneys that accurately represent human kidneys for biomedical screening and replacement therapies."
The new, open-source data, available at http://www.gudmap.org, provides the first systematic, high-resolution atlas or databank for human kidney genesis.
USC Stem Cell researchers analyzed the developmental differences in scale, timing and basic structure between human and mouse kidneys. They gained insight into the regulatory processes that maintain, expand and turn kidney stem cells into mature, functional kidney structures by examining human kidneys at different stages of development and juxtaposing their observations with mouse kidneys.
Researchers compared 26 human kidney "anchor genes" with their mouse equivalents. Kidney anchor genes are required for organ development. Only three genes (11 percent) have comparable expression between mouse and human kidneys: SLC22A6, ENTPD5 and UMOD.
"If the goal is to treat human kidney disease, clearly, it's better to focus on genes that are also active in human kidneys," Dr. McMahon said.
The median wait time for a kidney transplant is 3.6 years, meaning people have to put their lives on standby for years as they go to three dialysis appointments per week.
Kidney disease is a big, intractable problem, so it requires a multidisciplinary approach. That's why Dr. McMahon teamed up with Carl Kesselman, Ph.D., study co-author and professor of industrial and systems engineering at USC Viterbi.
Dr. Kesselman and his team at the Information Sciences Institute at USC Viterbi built software that automated many of the tasks researchers needed to perform, such as recording data observed by a high-resolution microscope. The tool not only fast-tracked one of the three studies but also created an online, searchable library to help other stem cell scientists in their kidney disease research.
"If you think of data as the modern version of a book, we gave the researcher tools to write the book, made the library where the book is stored and created a catalog system so others can find the book and check it out," said Dr. Kesselman.
To achieve this, Dr. Kesselman's team created DERIVA (Discovery Environment for Relational Information and Versioned Assets), a software program that collected data from microscopes and organized them and other study data into virtual photo albums that easily can be shared with other researchers.
"It's the difference between taking a photo with film or taking it with your smartphone and using the metadata that is automatically generated to organize your photos," Dr. Kesselman said. "At some point, you have so many photos that they become unmanageable. You can't find the one you want. DERIVA automatically catalogs your data so you can analyze massive amounts of data with Zen-like calm and share them with all of your friends throughout the world."
At an early stage, a nephron forming in the human kidney generates an S-shaped structure. Green cells will generate the kidneys’ filtering device, and blue and red cells are responsible for distinct nephron activities. Image courtesy of Stacy Moroz and Tracy Tran, Andrew McMahon Lab, USC Stem Cell.