Perturbations in Osteogenic Cell Fate Following Exposure to Constituents Present in Tobacco: A Combinatorial Study
Joseph V Madrid1, Madeline K M Vera-Colón1, Nicole I Zur Nieden1
1Department of Molecular, Cell & Systems Biology and Stem Cell Center, College of Natural and Agricultural Sciences, University of California Riverside, Riverside, CA 92521, USA.
Abstract:
Tobacco smoke contains between 7000 and 10,000 constituents, and only an evanescently low number of which have been identified, let alone been evaluated for their toxicity. Recently, the Food and Drug Administration has published a list of 93 chemical tobacco constituents that are harmful or potentially harmful to a number of cellular processes. However, their effect on developing skeletal cells is unknown. In this study, we used ToxPI, a computational tool, to prioritize constituents on this list for screening in osteogenically differentiating human embryonic stem cells and fibroblasts. In selected endpoint assays, we evaluated the potential of these chemicals to inhibit osteogenic differentiation success as well as their cytotoxicity. Six of these chemicals, which were ascribed an embryotoxic potential in our screen, as well as nicotine, which was not found to be osteotoxic in vitro, were then evaluated in combinatorial exposures, either in pairs of two or three. No one single chemical could be pinpointed as the culprit of reduced calcification in response to tobacco exposure. Combining chemicals at their half-maximal inhibitory concentration of differentiation often elicited expected decreases in calcification over the individual exposures; however, cytotoxicity was improved in many of the dual combinations. A reverse response was also noted, in which calcification output improved in combinatorial exposures. Results from ternary combinations reflected those from double combinations. Thus, the results from this study suggest that it may be difficult to isolate single chemicals as the primary drivers of skeletal embryotoxicity and that the full combination of chemicals in tobacco smoke may produce the hypomineralization phenotype that we have so far observed in vitro in human embryonic stem cells as well as in vivo in zebrafish.
Insights
Identifying specific toxic chemicals in tobacco smoke that harm skeletal development is challenging. Combinations of chemicals, not single agents, likely cause reduced bone formation, impacting embryonic stem cells and zebrafish development.
Area of Science:
- Toxicology
- Developmental Biology
- Stem Cell Research
Background:
- Tobacco smoke contains thousands of chemicals, with limited toxicity data.
- The Food and Drug Administration identified 93 harmful chemical constituents in tobacco.
- The impact of these chemicals on skeletal cell development remains largely unknown.
Purpose of the Study:
- To computationally prioritize and screen tobacco constituents for effects on osteogenic differentiation.
- To evaluate the cytotoxicity and osteogenic inhibitory potential of selected tobacco chemicals.
- To investigate the effects of combinatorial exposures of tobacco constituents on skeletal development.
Main Methods:
- Utilized ToxPI computational tool for prioritizing chemical constituents.
- Screened prioritized chemicals using osteogenically differentiating human embryonic stem cells and fibroblasts.
- Assessed inhibition of osteogenic differentiation and cytotoxicity.
- Evaluated effects of binary and ternary combinations of selected chemicals.
Main Results:
- Six chemicals showed embryotoxic potential; nicotine was not osteotoxic in vitro.
- No single chemical was identified as the sole cause of reduced calcification.
- Combinatorial exposures often decreased calcification but sometimes improved cytotoxicity.
- Observed a reverse response where calcification output improved in some combinations.
Conclusions:
- Isolating single chemicals responsible for skeletal embryotoxicity is difficult.
- The complex mixture of chemicals in tobacco smoke likely causes hypomineralization.
- Findings observed in human embryonic stem cells may translate to in vivo models like zebrafish.
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