A new system developed by scientists at the Morgridge Institute for Research and the University of Wisconsin-Madison may provide a faster, cheaper and more biologically relevant way to screen drugs and chemicals that could harm the developing brain.
Reporting in the Sept. 21, 2015 issue of the Proceedings of the National Academy of Sciences (PNAS), the team describes a new approach for predicting developmental neurotoxicity that uses stem cells to model features of the developing human brain that could be targeted by toxic chemicals or drugs.
The research also is important to addressing growing concerns about the rising incidence worldwide of neurodevelopmental disorders such as autism and the potential role of environmental chemicals.
First, the team produced a model human neural tissue by culturing stem cell-derived neural progenitor cells, vascular cells, and microglia on engineered hydrogels. These precursor cells self-assembled into three-dimensional neural tissue constructs with features that resemble the developing human brain. Such tissues are often referred to as “organoids.”
“Several things about this project surprised us,” says Michael Schwartz, an assistant scientist in biomedical engineering at UW-Madison and co-lead author of the study with Zhonggang Hou of the Morgridge Institute (now a researcher at Harvard University). “In the beginning, we weren’t expecting the kind of complex neural tissues that were ultimately developed.”
RNA-sequencing data was collected from neural tissue constructs that were individually exposed to 60 different “training” chemicals — both safe compounds and known toxins — and machine learning was used to build a predictive model from these results. The algorithm proved remarkably accurate: After training with known chemicals using duplicate samples and two time points (240 neural constructs in total), the model correctly classified nine out of 10 additional chemicals in a blinded trial.
Schwartz says that this new screening method offers a valuable bridge between testing a single layer of cells in a dish and testing on animals. “These model neural tissues capture a lot more of the complexity than you would find in a monolayer of cells,” he says. “They also mimic human physiology, and should be more relevant for predicting toxicity than animal models. The fact that we could apply a machine learning model to achieve 90 percent accuracy this early in the process is fantastic.”
This project reflects a diverse collaboration between the Morgridge Institute’s regenerative biology team, led by stem cell pioneer James Thomson, and leading UW-Madison experts in tissue engineering and machine learning.
Biomedical Engineering Professor William Murphy led the development of synthetic “hydrogels,” or matrices that enable stem cells to grow naturally and self-assemble into a complex network of tissues. And Biostatistics and Medical Informatics Professor David Page developed the predictive model using two types of holdout-testing methods.
Thomson says the Wisconsin project has potential to improve drug testing, but with more than 100,000 mostly untested chemical compounds used in commerce, the impact could be even greater for screening chemicals.
“The current toxicity screening tests use multi-generational rat studies and cost about $1 million to test one chemical,” he says. “So we need a really high-throughput way to test these compounds, figure out which ones may be the bad actors, then focus on those with more traditional methods.”
Schwartz says the RNA sequencing data generated by this study will be beneficial to future studies by helping to identify potential toxic profiles or fingerprints. “These datasets provide valuable information about changes in gene expression that researchers can mine to better understand mechanisms that might be disrupted during human brain development,” he says.
One unique element of the project is the level of consistency achieved across hundreds of samples — especially given the cellular diversity of the neural tissue model, which included neurons, glial cells, interconnected vascular networks, and microglia, which is the immune cell of central nervous system. The neural tissue constructs developed in this project are the first to incorporate vascular and microglial components into a 3D model of brain development derived from human pluripotent stem cells.
The synthetic material used to help the tissues grow was a key part of the early success of this work. “These hydrogels are minimally complex in that they only present peptides that allow the cells to attach and degrade the matrix. The cells will do the rest of the work on their own — biology does a better job forming tissues than we do,” Schwartz says.
In the original proposal, Thomson notes that “if appropriately specified, precursor cells are brought together in the right environment, a degree of self-assembly, differentiation, and maturation will occur.” The synthetic materials used to culture the cells were key to achieving the consistency needed to successfully screen so many samples.
Other co-authors of the study include: Nicholas Propson, Jue Zhang Peng Jiang, Bao Kim Nguyen, Ron Stewart and Yu Wang, Morgridge Institute; Collin Engstrom, Biostatistics and Medical Informatics and Computer Science; Victor Santos Costa, University of Porto, Portugal; and William Daly, Biomedical Engineering.
Funding: The National Institutes of Health (NIH) funded this project along with 10 other universities in the Tissue Chip for Drug Screening program. The Environmental Protection Agency (EPA) provided the list of well-characterized toxic and non-toxic chemicals used in the study.
Source: Michael Schwartz – Morgridge Institute for Research
Image Credit: The image is credited to Michael Schwartz, Department of Biomedical Engineering, UW-Madison
Original Research: Full open access research for “Human pluripotent stem cell-derived neural constructs for predicting neural toxicity” by Michael P. Schwartz, Zhonggang Hou, Nicholas E. Propson, Jue Zhang, Collin J. Engstrom, Vitor Santos Costa, Peng Jiang, Bao Kim Nguyen, Jennifer M. Bolin, William Daly, Yu Wang, Ron Stewart, C. David Page, William L. Murphy, and James A. Thomson in PNAS. Published online September 21 2015 doi:10.1073/pnas.1516645112
Abstract
Human pluripotent stem cell-derived neural constructs for predicting neural toxicity
Human pluripotent stem cell-based in vitro models that reflect human physiology have the potential to reduce the number of drug failures in clinical trials and offer a cost-effective approach for assessing chemical safety. Here, human embryonic stem (ES) cell-derived neural progenitor cells, endothelial cells, mesenchymal stem cells, and microglia/macrophage precursors were combined on chemically defined polyethylene glycol hydrogels and cultured in serum-free medium to model cellular interactions within the developing brain. The precursors self-assembled into 3D neural constructs with diverse neuronal and glial populations, interconnected vascular networks, and ramified microglia. Replicate constructs were reproducible by RNA sequencing (RNA-Seq) and expressed neurogenesis, vasculature development, and microglia genes. Linear support vector machines were used to construct a predictive model from RNA-Seq data for 240 neural constructs treated with 34 toxic and 26 nontoxic chemicals. The predictive model was evaluated using two standard hold-out testing methods: a nearly unbiased leave-one-out cross-validation for the 60 training compounds and an unbiased blinded trial using a single hold-out set of 10 additional chemicals. The linear support vector produced an estimate for future data of 0.91 in the cross-validation experiment and correctly classified 9 of 10 chemicals in the blinded trial.
“Human pluripotent stem cell-derived neural constructs for predicting neural toxicity” by Michael P. Schwartz, Zhonggang Hou, Nicholas E. Propson, Jue Zhang, Collin J. Engstrom, Vitor Santos Costa, Peng Jiang, Bao Kim Nguyen, Jennifer M. Bolin, William Daly, Yu Wang, Ron Stewart, C. David Page, William L. Murphy, and James A. Thomson in PNAS. Published online September 21 2015 doi:10.1073/pnas.1516645112
