The need to identify chemicals for their potential to cause reproductive and developmental (R/D) toxicity (R/D) is a significant public health challenge for toxicologists. In vivo testing for reproductive and developmental toxicity assessment uses a large number of animals, yet these studies are criticized for their inefficiency. The National Research Council (NRC)?s report ?Toxicity Testing in the 21st Century? envisioned that in vivo animal testing will eventually be replaced by a combination of in silico and in vitro approaches. Therefore, the need to identify in vitro systems for reproductive and developmental toxicity testing has grown. ReproTOX has established an animal-free testicular cell co-culture system (Mini-Testis) from testicular cell lines. Both morphology and cellular biomarkers confirmed that this animal-free 3D-co-culture model support in vitro spermatogenesis. Our 32-compound preliminary study revealed a stronger correlation of IC50 from the Mini-Testis model with in vivo reproductive toxicity as compared to any single testicular cell culture model. These initial results suggest that our Mini-Testis model might be a valuable screening tool for reproductive toxicants and prioritizing chemicals for further testing.
The specific aims of this proposal, therefore, are to (1) establish a toxicity-based high throughput Mini-Testis model for R/D toxicity evaluation and (2) develop an integrated pathway-based high content (HCA) and high throughput (HT) screening assay in the Mini-Testis model for R/D toxicity evaluation. The project outcome will be a cost-efficient, pathway-based in vitro Mini- Testis model for potential R/D toxicity screening of chemicals.

Public Health Relevance

We will establish and develop a toxicity-based high throughput screening (HTS) and pathway-based high content (HCA) assay for R/D toxicity evaluation. This pathway-based in vitro Mini-Testis model will contribute significantly to public health by providing a cost-efficient way to screen the chemicals for the potential R/D toxicity.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Small Business Innovation Research Grants (SBIR) - Phase I (R43)
Project #
1R43ES027374-01
Application #
9198371
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Shaughnessy, Daniel
Project Start
2016-08-01
Project End
2017-01-31
Budget Start
2016-08-01
Budget End
2017-01-31
Support Year
1
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Reprotox Biotech, LLC
Department
Type
DUNS #
079938404
City
Athens
State
GA
Country
United States
Zip Code
30602
Siracusa, Jacob Steven; Yin, Lei; Measel, Emily et al. (2018) Effects of bisphenol A and its analogs on reproductive health: A mini review. Reprod Toxicol 79:96-123
Yin, Lei; Wei, Hongye; Liang, Shenxuan et al. (2017) From the Cover: An Animal-Free In Vitro Three-Dimensional Testicular Cell Coculture Model for Evaluating Male Reproductive Toxicants. Toxicol Sci 159:307-326
Liang, Shenxuan; Yin, Lei; Shengyang Yu, Kevin et al. (2017) High-Content Analysis Provides Mechanistic Insights into the Testicular Toxicity of Bisphenol A and Selected Analogues in Mouse Spermatogonial Cells. Toxicol Sci 155:43-60