Author:
Byrne A. T.,Southgate J.,Brison D. R.,Leese H. J.
Abstract
The proposition that members of the insulin-like growth factor superfamily act
as rescue factors from apoptosis in murine preimplantation embryos was tested.
The cytokine tumour necrosis factor α (TNFα) was used to induce
apoptosis. Zygotes were cultured for 5 days to the blastocyst stage in the
presence or absence of TNFα and in the presence or absence of the
insulin-like growth factors, IGF-I or IGF-II. Tumour necrosis factor α
significantly increased the percentage of apoptotic cells and reduced the
total cell count in Day 5 blastocysts. When IGF-I or IGF-II were added to the
culture medium in the presence of TNFα, the cell number and apoptotic
dead cell index (DCI) were restored to control values. Insulin-like growth
factor-I alone had a greater effect on total cell number than IGF-II alone,
but did not significantly decrease the apoptotic DCI. In contrast, IGF-II
significantly reduced the number of apoptotic cells. This study shows that
IGFs may play a role as apoptotic survival factors in the early mouse embryo.
Subject
Developmental Biology,Endocrinology,Genetics,Molecular Biology,Animal Science and Zoology,Reproductive Medicine,Biotechnology
Cited by
45 articles.
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