Abstract
Given the vast number of chemicals that are released into the environment each year, it is imperative that we develop new predictive models to identify toxicants before unavoidable exposure harms the health of humans and other organisms. In vitro models are especially attractive in predictive toxicology as they can greatly reduce assay costs and animal usage while identifying those chemicals that may require further in vivo evaluation. With the derivation of both mouse and human embryonic stem cells, new opportunities have developed that could revolutionize the field of predictive toxicology. Stem cells themselves can be used to model the earliest stages of development, or they can be differentiated to study later aspects of development. Because embryos and fetuses are usually more sensitive to environmental toxicants than adults, stem cells provide an unique tool for studying the prenatal phase in our life cycle. The embryonic stem cell test (EST), which has been validated for use with mouse embryonic stem cells (mESC), is an accurate predictor of embryotoxic compounds, particularly those that are highly embryotoxic. Human embryonic stem cells (hESCs), although not yet incorporated into a validated test, are a particularly attractive platform for toxicological testing as they can give us direct information on humans and avoid concerns about species variation in response. This review discusses toxicological studies and strategies that have been used with embryonic stem cells during the past five years and possible directions that could lead to improvements in the development of predictive assays in the future.
Keywords: development of predictive assays, fetuses, toxicants, harm reduction cigarettes, cigarette smoke, embryonic stem cell test, drug testing, toxicological testing, predictive toxicology, embryonic stem cells, In vitro assays
Current Topics in Medicinal Chemistry
Title: Mouse and Human Embryonic Stem Cells: Can They Improve Human Health by Preventing Disease?
Volume: 11 Issue: 13
Author(s): Sabrina Lin and Prue Talbot
Affiliation:
Keywords: development of predictive assays, fetuses, toxicants, harm reduction cigarettes, cigarette smoke, embryonic stem cell test, drug testing, toxicological testing, predictive toxicology, embryonic stem cells, In vitro assays
Abstract: Given the vast number of chemicals that are released into the environment each year, it is imperative that we develop new predictive models to identify toxicants before unavoidable exposure harms the health of humans and other organisms. In vitro models are especially attractive in predictive toxicology as they can greatly reduce assay costs and animal usage while identifying those chemicals that may require further in vivo evaluation. With the derivation of both mouse and human embryonic stem cells, new opportunities have developed that could revolutionize the field of predictive toxicology. Stem cells themselves can be used to model the earliest stages of development, or they can be differentiated to study later aspects of development. Because embryos and fetuses are usually more sensitive to environmental toxicants than adults, stem cells provide an unique tool for studying the prenatal phase in our life cycle. The embryonic stem cell test (EST), which has been validated for use with mouse embryonic stem cells (mESC), is an accurate predictor of embryotoxic compounds, particularly those that are highly embryotoxic. Human embryonic stem cells (hESCs), although not yet incorporated into a validated test, are a particularly attractive platform for toxicological testing as they can give us direct information on humans and avoid concerns about species variation in response. This review discusses toxicological studies and strategies that have been used with embryonic stem cells during the past five years and possible directions that could lead to improvements in the development of predictive assays in the future.
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Cite this article as:
Lin Sabrina and Talbot Prue, Mouse and Human Embryonic Stem Cells: Can They Improve Human Health by Preventing Disease?, Current Topics in Medicinal Chemistry 2011; 11 (13) . https://dx.doi.org/10.2174/156802611796117621
DOI https://dx.doi.org/10.2174/156802611796117621 |
Print ISSN 1568-0266 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-4294 |
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