| Literature DB >> 29145065 |
Renee E Albers1, Christopher A Waker1, Chanel Keoni1, Melissa R Kaufman1, Michael A Bottomley2, Sarah Min3, David R Natale3, Thomas L Brown4.
Abstract
The placenta is a complex and essential organ composed largely of fetal-derived cells, including several different trophoblast subtypes that work in unison to support nutrient transport to the fetus during pregnancy. Abnormal placental development can lead to pregnancy-associated disorders that often involve metabolic dysfunction. The scope of dysregulated metabolism during placental development may not be fully representative of the in vivo state in defined culture systems, such as cell lines or isolated primary cells. Thus, assessing metabolic function in intact placental tissue would provide a better assessment of placental metabolism. In this study, we describe a methodology for assaying glycolytic function in structurally-intact mouse placental tissue, ex vivo, without culturing or tissue dissociation, that more closely resembles the in vivo state. Additionally, we present data highlighting sex-dependent differences of two mouse strains (C57BL/6 and ICR) in the pre-hypertrophic (E14.5) and hypertrophic (E18.5) placenta. These data establish a foundation for investigation of metabolism throughout gestation and provides a comprehensive assessment of glycolytic function during placental development.Entities:
Keywords: Extracellular flux; Ex vivo; Glycolysis; Metabolism; Placenta; Sexual dimorphism; Tissue
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Year: 2017 PMID: 29145065 PMCID: PMC5725248 DOI: 10.1016/j.theriogenology.2017.10.049
Source DB: PubMed Journal: Theriogenology ISSN: 0093-691X Impact factor: 2.740