Mitochondrial energetics and contents evaluated by flow cytometry in human maternal and umbilical cord blood

脐带 流式细胞术 能量学 男科 脐带血 能量代谢 胎儿 血流 化学 医学 产科 生物 怀孕 免疫学 内科学 遗传学 生态学
作者
Julie Kristine Guldberg Stryhn,Jacob Larsen,Palle Pedersen,Anne-Dorthe Feldthusen,Jan Kvetny,Peter Gæde
出处
期刊:Scandinavian Journal of Clinical & Laboratory Investigation [Informa]
卷期号:80 (5): 351-359 被引量:3
标识
DOI:10.1080/00365513.2020.1768584
摘要

Background: Mitochondrial dysfunction may relate to metabolic disorders. The relation between maternal and fetal mitochondrial function needs attention due to heritage.Objectives: To evaluate the use of the staining methods TetraMethylRhodamine Methyl Ester (TMRM) and Mitotracker Green (MTG) for flow cytometric measurements of umbilical cord blood mitochondrial function. Methods: 53 euthyroid at-term pregnant women and their offspring were included by blood collections. The offspring had blood drawn from the clamped umbilical cord. Flow cytometry with MTG, TMRM and Propidium Iodide were performed the following day. A cell count (antibody coating and flow cytometry) was performed for 9 maternal and cord samples. As a quality control, blood of 32 healthy donors was evaluated by flow cytometric analyzes same day as sampling and the following day to test stability of the measurements.Results: Cord mitochondrial measurements were lower than maternal. Maternal and cord mitochondrial function were positively correlated, especially reflected by MTG fluorescence-intensity (FI). Samples stored presented with very changed fluorescence patterns. However, the fluorescence intensity ratios MTG/TMRM of stained white blood cells were related within same day measurements, depicting an extensive and common bioenergetic cellular change.Conclusion: Cord blood flow cytometry by MTG- and TMRM- staining is possible with fluorescence intensity positively correlated to maternal fluorescence intensity. Storage of blood triggers mitochondrial dynamics. The methods are applicable with certain reservations, and they benefit from their non-invasive character compared to mitochondrial evaluation by muscle-biopsies.
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