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Human Pluripotent Stem Cell Based Developmental Toxicity Assays for Chemical Safety Screening and Systems Biology Data Generation
Published on: June 17, 2015
Human Pluripotent Stem Cell-Based Assays to Predict Developmental Toxicity
Madhura Banerjee1, Aritrika Das1, Prarthana Chatterjee1
1School of BioSciences and Technology, Vellore Institute of Technology, Vellore, India.
Abstract:
Human beings are continuously exposed to various toxic substances throughout their lives, which affect their reproductive health and eventually the offspring they give birth to. Mainly, these toxins damage the heart and neurological development of the newborn, but most recently, they have begun to affect the musculoskeletal system as well. These toxins are usually present in food, pharmaceuticals, cosmetics, or even the polluted air that people breathe; as a result, the prevalence of birth defects is steadily rising. For this reason, it becomes a necessity to deploy a new set of assays to test for such toxins in industries to decrease the occurrence of developmental toxicity. These assays are exceedingly expensive when carried out conventionally using animal models or cells from such sources and have a lower predictive value due to the vast variation between animals and humans. To overcome such major problems, human pluripotent stem cells are now frequently used for these assays. These cells are easily available, are quickly generated from somatic cells (induce pluripotent stem cells), can be of human origin without harming people, and eliminate animal harm, which makes them the top choice of scientists for carrying out any in vitro developmental toxicity assays.This chapter, therefore, provides an overview of several steps that can be used to predict a compound's developmental toxicity by utilizing human pluripotent stem cells. Here, the easiest and most effective procedure has been outlined that can screen many compounds simultaneously.
Insights
Environmental toxins harm reproductive health and offspring development. Human pluripotent stem cells offer a cost-effective, ethical alternative for developmental toxicity assays, improving prediction accuracy.
Area of Science:
- Toxicology
- Developmental Biology
- Stem Cell Research
Background:
- Human exposure to environmental toxins impacts reproductive health and offspring development, affecting neurological, cardiac, and musculoskeletal systems.
- Rising prevalence of birth defects necessitates improved methods for detecting developmental toxicity.
- Conventional toxicity assays using animal models are expensive, ethically problematic, and have limited predictive value due to interspecies variation.
Purpose of the Study:
- To provide an overview of methods for predicting compound developmental toxicity using human pluripotent stem cells.
- To outline an efficient and effective procedure for high-throughput screening of developmental toxicants.
- To highlight the advantages of human pluripotent stem cells in toxicity testing.
Main Methods:
- Utilizing human pluripotent stem cells, including induced pluripotent stem cells, for in vitro developmental toxicity assays.
- Developing and presenting a streamlined protocol for simultaneous screening of multiple compounds.
- Focusing on assays that leverage the human origin and accessibility of pluripotent stem cells.
Main Results:
- Human pluripotent stem cells provide a viable alternative to animal models for developmental toxicity testing.
- The outlined procedure enables simultaneous screening of numerous compounds, increasing efficiency.
- This approach offers a more predictive and ethically sound method for assessing developmental toxicity.
Conclusions:
- Human pluripotent stem cells are a superior choice for in vitro developmental toxicity assays due to their accessibility, human origin, and ethical advantages.
- The presented methodology offers a cost-effective and highly predictive approach to screening for developmental toxicants.
- Implementing these assays can significantly reduce the occurrence of birth defects linked to toxic substance exposure.
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