Probing morphological, genetic and metabolomic changes of in vitro embryo development in a microfluidic device.

Autor: Mancini V; School of Electronic and Electrical Engineering, University of Leeds, Leeds, UK., McKeegan PJ; Reproduction and Early Development Research Group, Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, School of Medicine, University of Leeds, UK.; Centre for Anatomical and Human Sciences, Hull York Medical School, University of Hull, Hull, UK., Schrimpe-Rutledge AC; Center for Innovative Technology (CIT), Department of Chemistry, Vanderbilt University, Nashville, Tennessee, USA., Codreanu SG; Center for Innovative Technology (CIT), Department of Chemistry, Vanderbilt University, Nashville, Tennessee, USA., Sherrod SD; Center for Innovative Technology (CIT), Department of Chemistry, Vanderbilt University, Nashville, Tennessee, USA., McLean JA; Center for Innovative Technology (CIT), Department of Chemistry, Vanderbilt University, Nashville, Tennessee, USA., Picton HM; Reproduction and Early Development Research Group, Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, School of Medicine, University of Leeds, UK., Pensabene V; School of Electronic and Electrical Engineering, University of Leeds, Leeds, UK.; Leeds Institute of Medical Research, University of Leeds, UK.
Jazyk: angličtina
Zdroj: Biotechnology progress [Biotechnol Prog] 2021 Nov; Vol. 37 (6), pp. e3194. Date of Electronic Publication: 2021 Jul 29.
DOI: 10.1002/btpr.3194
Abstrakt: Assisted reproduction technologies for clinical and research purposes rely on a brief in vitro embryo culture which, despite decades of progress, remain suboptimal in comparison to the physiological environment. One promising tool to improve this technique is the development of bespoke microfluidic chambers. Here we present and validate a new microfluidic device in polydimethylsiloxane (PDMS) for the culture of early mouse embryos. Device material and design resulted embryo compatible and elicit minimal stress. Blastocyst formation, hatching, attachment and outgrowth formation on fibronectin-coated devices were similar to traditional microdrop methods. Total blastocyst cell number and allocation to the trophectoderm and inner cell mass lineages were unaffected. The devices were designed for culture of 10-12 embryos. Development rates, mitochondrial polarization and metabolic turnover of key energy substrates glucose, pyruvate and lactate were consistent with groups of 10 embryos in microdrop controls. Increasing group size to 40 embryos per device was associated with increased variation in development rates and altered metabolism. Device culture did not perturb blastocyst gene expression but did elicit changes in embryo metabolome, which can be ascribed to substrate leaching from PDMS and warrant further investigation.
(© 2021 The Authors. Biotechnology Progress published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers.)
Databáze: MEDLINE
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