2011Journal of International Reproductive Health/Family PlanningRequires access

Effect of IGF-II and EGF on the Development of ICR Mouse Embryos in Vitro

Zhou Hong-li

Open publisher page 0 citations

Abstract

Objective: To investigate the effection of IGF-Ⅱ and EGF on the development of ICR mouse preimplantation embryos in the CZB culture medium with glucose and insulin in vitro.Methods: ①Experiment1: One-cell ICR mouse embryos were cultured in the CZB medium with glucose and insulin supplemented with IGF-Ⅱ(0,0.1,1,10 and 100 μg/L),and a separate control group of CZB medium was established.②Experiment 2: One-cell ICR mouse embryos were cultured in the CZB medium with glucose,insulin and IGF-Ⅱ(0.1 μg/L) supplemented with EGF(0,0.1,1,10 and 100 μg/L),and a separate control group of CZB medium was established.Blastocyst rates,hatched blastocyst rates and the cell numbers of blastocysts were counted.Results: ①Experiment1: IGF-Ⅱ(0 μg/L) increased the rate of blastocyst,hatched blastocyst and the total cell numbers of blastocyst compared with control group(P0.05).IGF-Ⅱat a dose of 100 μg/L decreased the rate of blastocyst,hatched blastocyst and the total cell numbers of blastocyst compared with the other groups(P0.05).IGF-Ⅱ at a dose of 0.1 μg/L greatly increased the total cell numbers of blastocyst(P0.05).②Experiment 2: EGF(0 μg/L) increased the rate of blastocyst,hatched blastocyst and the total cell numbers of blastocyst compared with control group(P0.05).EGF at doses of 0.1,1 and 10 μg/L increased the rate of blastocyst and hatched blastocyst compared with EGF at doses of 0 and 100 μg/L(P0.05),and EGF at a dose of 0.1 μg/L had the highest rate of hatched blastocyst(P0.05).EGF at a dose of 0.1 μg/L increased the total cell numbers of blastocyst compared with EGF at a dose of 0 μg/L(P0.05).EGF at a dose of 100 μg/L had the lowest rate of the total cell numbers of blastocyst(P0.05).Conclusions: ①IGF-Ⅱ(1,10 μg/L),glucose and insulin showed no significant effect of suppression or promotion among.②EGF(1,10 μg/L) in CZB medium with glucose,insulin and IGF-Ⅱcould involves in the regulationof differentiation of embryonic cells but no proliferation.③IGF-Ⅱ and EGF at a dose of 0.1 μg/L is best for cell culture concentration.④IGF-Ⅱ and EGF at a dose of 100 μg/L have inhibition effect on embryonic cells.

About this research paper

What this paper is about

Objective: To investigate the effection of IGF-Ⅱ and EGF on the development of ICR mouse preimplantation embryos in the CZB culture medium with glucose and insulin in vitro.Methods: ①Experiment1: One-cell ICR mouse embryos were cultured in the CZB medium with glucose and insulin supplemented with IGF-Ⅱ(0,0.1,1,10 and 100 μg/L),and a separate control group of CZB medium was established.②Experiment 2: One-cell ICR mouse embryos were cultured in the CZB medium with glucose,insulin and IGF-Ⅱ(0.1 μg/L) supplemented with EGF(0,0.1,1,10 and 100 μg/L),and a separate control group of CZB medium was established.Blastocyst rates,hatched blastocyst rates and the cell numbers of blastocysts were counted.Results: ①Experiment1: IGF-Ⅱ(0 μg/L) increased the rate of blastocyst,hatched blastocyst and the total cell numbers of blastocyst compared with control group(P0.05).IGF-Ⅱat a dose of 100 μg/L decreased the rate of blastocyst,hatched blastocyst and the total cell numbers of blastocyst compared with the other groups(P0.05).IGF-Ⅱ at a dose of 0.1 μg/L greatly increased the total cell numbers of blastocyst(P0.05).②Experiment 2: EGF(0 μg/L) increased the rate of blastocyst,hatched blastocyst and the total cell numbers of blastocyst compared with control group(P0.05).EGF at doses of 0.1,1 and 10 μg/L increased the rate of blastocyst and hatched blastocyst compared with EGF at doses of 0 and 100 μg/L(P0.05),and EGF at a dose of 0.1 μg/L had the highest rate of hatched blastocyst(P0.05).EGF at a dose of 0.1 μg/L increased the total cell numbers of blastocyst compared with EGF at a dose of 0 μg/L(P0.05).EGF at a dose of 100 μg/L had the lowest rate of the total cell numbers of blastocyst(P0.05).Conclusions: ①IGF-Ⅱ(1,10 μg/L),glucose and insulin showed no significant effect of suppression or promotion among.②EGF(1,10 μg/L) in CZB medium with glucose,insulin and IGF-Ⅱcould involves in the regulationof differentiation of embryonic cells but no proliferation.③IGF-Ⅱ and EGF at a dose of 0.1 μg/L is best for cell culture concentration.④IGF-Ⅱ and EGF at a dose of 100 μg/L have inhibition effect on embryonic cells.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective: To investigate the effection of IGF-Ⅱ and EGF on the development of ICR mouse preimplantation embryos in the CZB culture medium with glucose and insulin in vitro.Methods: ①Experiment1: One-cell ICR mouse embryos were cultured in the CZB medium with glucose and insulin supplemented with IGF-Ⅱ(0,0.1,1,10 and 100 μg/L),and a separate control group of CZB medium was established.②Experiment 2: One-cell ICR mouse embryos were cultured in the CZB medium with glucose,insulin and IGF-Ⅱ(0.1 μg/L) supplemented with EGF(0,0.1,1,10 and 100 μg/L),and a separate control group of CZB medium was established.Blastocyst rates,hatched blastocyst rates and the cell numbers of blastocysts were counted.Results: ①Experiment1: IGF-Ⅱ(0 μg/L) increased the rate of blastocyst,hatched blastocyst and the total cell numbers of blastocyst compared with control group(P0.05).IGF-Ⅱat a dose of 100 μg/L decreased the rate of blastocyst,hatched blastocyst and the total cell numbers of blastocyst compared with the other groups(P0.05).IGF-Ⅱ at a dose of 0.1 μg/L greatly increased the total cell numbers of blastocyst(P0.05).②Experiment 2: EGF(0 μg/L) increased the rate of blastocyst,hatched blastocyst and the total cell numbers of blastocyst compared with control group(P0.05).EGF at doses of 0.1,1 and 10 μg/L increased the rate of blastocyst and hatched blastocyst compared with EGF at doses of 0 and 100 μg/L(P0.05),and EGF at a dose of 0.1 μg/L had the highest rate of hatched blastocyst(P0.05).EGF at a dose of 0.1 μg/L increased the total cell numbers of blastocyst compared with EGF at a dose of 0 μg/L(P0.05).EGF at a dose of 100 μg/L had the lowest rate of the total cell numbers of blastocyst(P0.05).Conclusions: ①IGF-Ⅱ(1,10 μg/L),glucose and insulin showed no significant effect of suppression or promotion among.②EGF(1,10 μg/L) in CZB medium with glucose,insulin and IGF-Ⅱcould involves in the regulationof differentiation of embryonic cells but no proliferation.③IGF-Ⅱ and EGF at a dose of 0.1 μg/L is best for cell culture concentration.④IGF-Ⅱ and EGF at a dose of 100 μg/L have inhibition effect on embryonic cells.

Key concepts: Blastocyst, Andrology, Embryo, In vitro, Biology, In vitro fertilisation, Endocrinology, Embryogenesis

Related papers

Back to paper searchBrowse research topicsOriginal source
Effect of IGF-II and EGF on the Development of ICR Mouse Embryos in Vitro — Research Paper | ScholarLens