Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/77386
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Type: Journal article
Title: Epiblast cell number and primary embryonic stem cell colony generation are increased by culture of cleavage stage embryos in insulin
Author: Campbell, J.
Lane, M.
Vassiliev, I.
Nottle, M.
Citation: Journal of Reproduction and Development, 2013; 59(2):131-138
Publisher: Japanese Soc Animal Reproduction
Issue Date: 2013
ISSN: 0916-8818
1348-4400
Statement of
Responsibility: 
J.M. Campbell, M. Lane, I. Vassiliev and M.B. Nottle
Abstract: Human embryos for hESC derivation are often donated at the cleavage stage and of reduced quality. Poor quality embryos have lower efficiency for hESC derivation. However, cleavage stage mouse embryos develop into higher quality expanded blastocysts if they are cultured with insulin, suggesting that this approach could be used to improve hESC derivation from poor quality cleavage stage embryos. The present study used a mouse model to examine this approach. In particular we examined the effect of insulin on the number of epiblast cells in blastocysts on days 4, 5 and 6 using Oct4 and Nanog co-expression. Second we examined the effect of insulin on the frequency with which outgrowths can be derived from these. Finally, we tested whether prior culture in the presence of insulin results in blastocysts with increased capacity to generate ESC colonies. Culture of cleavage stage embryos with insulin increased the number of Oct4 and Nanog positive cells in blastocysts at all time points examined. Prior culture with insulin had no effect on outgrowths generated from blastocysts plated on days 4 or 5. However, insulin treatment of blastocysts plated on day 6 resulted in increased numbers of outgrowths with larger epiblasts compared with controls. 13% of insulin treated day 6 blastocysts produced primary ESC colonies compared with 6% of controls. In conclusion, treatment with insulin can improve epiblast cell number in mice leading to an increase with which primary ESC colonies can be generated and may improve hESC isolation from reduced quality embryos donated at the cleavage stage.
Keywords: Blastocyst; Germ Layers; Animals; Mice; Insulin; Homeodomain Proteins; Hypoglycemic Agents; Embryo Culture Techniques; Cell Count; Octamer Transcription Factor-3; Embryonic Stem Cells; Nanog Homeobox Protein
Rights: © Society for Reproduction and Development
RMID: 0020126961
DOI: 10.1262/jrd.2012-103
Description (link): http://www.ncbi.nlm.nih.gov/pubmed/23171593
Appears in Collections:Obstetrics and Gynaecology publications

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