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Birth Defects Res A Clin Mol Teratol. 2014 Aug;100(8):623-32. doi: 10.1002/bdra.23272. Epub 2014 Aug 13.

Untargeted metabolite profiling of murine embryos to reveal metabolic perturbations associated with neural tube closure defects.

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  • 1Department of Pharmacology, Weill Cornell Medical College, New York, New York; Program in Pharmacology, Weill Cornell Medical College, New York, New York.

Abstract

BACKGROUND:

Neural tube closure defects (NTDs) are among the most common congenital malformation in human, typically presenting in liveborns as spina bifida. At least 240 gene mutations in mouse are known to increase the risk of NTD. There is a growing appreciation that environmental factors significantly contribute to NTD expression, and that NTDs likely arise from complex gene-environment interactions. Because maternal folic acid supplementation reduces human NTD risk in some populations by 60 to 70%, it is likely that NTD predisposition is often associated with a defect in folate-dependent one-carbon metabolism. A comprehensive, untargeted metabolic survey of NTD-associated changes in embryo metabolism would provide a valuable test of this assumption. We sought to establish a metabolic profiling platform that is capable of broadly assessing metabolic aberrations associated with NTD-promoting gene mutations in early-stage mouse embryos.

METHODS:

A liquid chromatography/mass spectrometry-based untargeted metabolite profiling platform was used to broadly identify significant differences in small molecule levels (50-1000 Da) in NTD-affected embryonic day (E) 9.5 mouse embryos (Lrp6(-) (/) (-) ) versus unaffected (Lrp6(+/+) ) control embryos.

RESULTS:

Results provide proof-of-principal feasibility for the broad survey of the metabolome of individual E9.5 mouse embryos and identification of metabolic changes associated with NTDs and gene mutations. Levels of 30 different metabolites were altered in association with Lrp6 gene deletion. Some metabolites link to folate-dependent one-carbon transfer reactions, as anticipated, while others await structure elucidation and pathway integration.

CONCLUSION:

Whole-embryo metabolomics offers the potential to identify metabolic changes in genetically determined NTD-prone embryos.

KEYWORDS:

closure defects; folate; neural tube

PMID:
25115437
PMCID:
PMC4146720
DOI:
10.1002/bdra.23272
[PubMed - indexed for MEDLINE]
Free PMC Article
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