Previous Page  105 / 129 Next Page
Information
Show Menu
Previous Page 105 / 129 Next Page
Page Background

Mechanobiology of Disease

Poster Abstracts

100

3-POS

Board 3

Comprehensive Analyses of Gene Expression Patterns in Early Mouse Early Embryos

Experiencing Chemical and Mechanical Stimuli

Yuka Asano

1,2

, Koji Matsuura

1,2

.Keiji Naruse

2

.

2

Okayama University, Okayama, Japan.

1

Okayama University of Science, Okayama, Japan,

In vitro

mammalian embryonic development can be enhanced by mimicking physiological

conditions, which can provide better infertility treatment. By comprehensive analyses of gene

expression, we evaluated differences in gene expression patterns of ICR mouse blastocysts

cultured

in vitro

from two-cell embryo stage using different media under a static or dynamic

culture system to subject the embryos to mechanical stimuli (MS). To compare the influences of

the medium on early mouse embryonic development, we used mW medium (mW-S) and KSOM

medium (KSOM-S) under static culture. The influences of MS in mW medium were investigated

using the tilting embryo culture system (TECS), which improves blastocyst development. We

compared the gene expression patterns between the TECS (mW-T) and mW-S groups.

Blastocyst development rates in the mW-S, KSOM-S, and mW-T groups were 62.6%, 94.1%,

and 70.8%, respectively (P < 0.01). We extracted total RNAs thrice from the three groups, and

the total number of blastocysts was approximately 80 × 9 = 720. RNA amplification, RNA-Seq

library preparation, and RNA sequencing were consigned to Hokkaido System Science Co. Ltd.

Upon comparison of the relative gene expression levels between the KSOM-S and mW-S

groups, the gene expression level in the trophectoderm (TE), which functions as a source of

embryonic nutrition, was improved in culture conditions under KSOM medium compared with

that in culture conditions under mW medium.

Tagln2

gene expression as a TE marker increased

(P < 0.01) under KSOM culture.

Gdf3

gene expression levels related to epiblast (EPI)

development in the mW-T group was higher than that in the mW-S group (P < 0.01). MS

improved EPI development under the same medium conditions. The expression patterns of EPI

and TE markers differed between the culture systems with chemical stimuli by medium and MS.

We consider that optimized medium components can improve both TE and EPI development and

that MS can improve the gene expression of EPI markers. However, the gene expression level

induced by MS would be relatively lower in TE than in EPI.