Published March 1, 2017
The skin cells of four adults with schizophrenia have provided an unprecedented “window” into how the disease began while they were still in the womb, according to a recent paper in Schizophrenia Research.
The paper was published online in January by researchers at the Jacobs School of Medicine and Biomedical Sciences at UB in collaboration with the Icahn School of Medicine at Mount Sinai. It provides what the authors call the first proof of concept for their hypothesis that a common genomic pathway lies at the root of schizophrenia.
The researchers say the work is a first step toward the design of treatments that could be administered to pregnant mothers at high risk for bearing a child with schizophrenia, potentially preventing the disease before it begins.
“In the last 10 years, genetic investigations into schizophrenia have been plagued by an ever-increasing number of mutations found in patients with the disease,” said Michal K. Stachowiak, the paper's senior author and professor in the Department of Pathology and Anatomical Sciences.
“We show for the first time that there is, indeed, a common, dysregulated gene pathway at work here,” he said.
The authors gained insight into the early brain pathology of schizophrenia by using skin cells from four adults with schizophrenia and four adults without the disease that were reprogrammed back into induced pluripotent stem cells and then into neuronal progenitor cells.
“By studying induced pluripotent stem cells developed from different patients, we recreated the process that takes place during early brain development in utero, thus obtaining an unprecedented view of how this disease develops,” said Stachowiak. “This work gives us an unprecedented insight into those processes.”
The research provides what he calls proof of concept for the hypothesis he and his colleagues published in 2013. They proposed that a single genomic pathway, called the Integrative Nuclear FGFR 1 Signaling (INFS), is a central intersection point for multiple pathways involving more than 100 genes believed to be involved in schizophrenia.
“This research shows that there is a common dysregulated gene program that may be impacting more than 1,000 genes and that the great majority of those genes are targeted by the dysregulated nuclear FGFR1,” Stachowiak said.
When even one of the many schizophrenia-linked genes undergoes mutation, by affecting the INFS it throws off the development of the brain as a whole, similar to the way that an entire orchestra can be affected by a musician playing just one wrong note, he said.
The next step in the research is to use these induced pluripotent stem cells to further study how the genome becomes dysregulated, allowing the disease to develop.
“We will utilize this strategy to grow cerebral organoids – essentially mini-brains – to determine how this genomic dysregulation affects early brain development and to test potential preventive or corrective treatments,” he said.
UB co-authors with Stachowiak are P. Sarder and E. K. Stachowiak, both assistant professors in the Department of Pathology and Anatomical Sciences, as well as S. Narla, Y-W Lee and C.A. Benson, all graduate students in the department. K.J. Brennand of the Icahn School of Medicine at Mt. Sinai also is a co-author.
The work is funded by NYSTEM, the Patrick P. Lee Foundation, the National Science Foundation and the National Institutes of Health.