Culshaw, LH;
Savery, D;
Greene, NDE;
Copp, AJ;
(2019)
Mouse whole embryo culture: Evaluating the requirement for rat serum as culture medium.
Birth Defects Research
, 111
(16)
pp. 1165-1177.
10.1002/bdr2.1538.
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Abstract
Background: Whole embryo culture is a valuable research method in mammalian developmental biology and birth defects research, enabling longitudinal studies of explanted organogenesis-stage rodent embryos. Rat serum is the primary culture medium, and can sustain growth and development over limited periods as in utero. However, the cost, labor, and time to produce culture serum are factors limiting the uptake of the methodology. The goal of replacing or at least reducing rat serum usage in culture would be in accordance with the principles of “replacement, reduction, and refinement” of animals in research (the 3Rs). Methods: We performed cultures of mouse embryos for 24 hr from embryonic day 8.5 in serum-free media or in rat serum diluted with defined media, compared with 100% rat serum. Developmental parameters scored after culture included yolk sac circulation, dorsal axial length, somite number, protein content, and completion of cranial neural tube closure. Results: A literature review revealed use of both serum-free and diluted rat serumbased media in whole embryo culture studies, but with almost no formal comparisons of culture success against 100% rat serum. Two serum-free media were tested, but neither could sustain development as in 100% rat serum. Dilution of rat serum 1:1 with Glasgow Minimum Essential Medium plus defined supplements supported growth and development as well as whole rat serum, whereas other diluent media yielded substandard outcomes. Conclusion: Rat serum usage cannot be avoided, to achieve high quality mouse embryo cultures, but rat usage can be reduced using medium containing diluted serum.
Type: | Article |
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Title: | Mouse whole embryo culture: Evaluating the requirement for rat serum as culture medium |
Location: | United States |
Open access status: | An open access version is available from UCL Discovery |
DOI: | 10.1002/bdr2.1538 |
Publisher version: | https://doi.org/10.1002/bdr2.1538 |
Language: | English |
Additional information: | This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. https://creativecommons.org/licenses/by/4.0/ |
Keywords: | birth defects, development, embryo culture, neural tube, organogenesis, postimplantation, teratogen, yolk sac |
UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health > Developmental Biology and Cancer Dept |
URI: | https://discovery-pp.ucl.ac.uk/id/eprint/10077064 |
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