## Abstract Blastocysts submitted to two rounds of immunosurgery give rise to cores of presumptive ectoderm cells, many of which do not survive for more than 48 hours when cultured individually. Precoating of the culture plates with conditioned medium (CM) from PYSβ2 cells increases the incidence w
Effect of antimetabolites on programming of inner cells of the mouse blastocyst
β Scribed by McCue, Peter A. ;Sherman, Michael I.
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 475 KB
- Volume
- 224
- Category
- Article
- ISSN
- 0022-104X
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β¦ Synopsis
Abstract
When early blastocysts are subjected to immunosurgery, the resulting inner cell masses (ICMs) regenerate trophoblast cells. In contrast, ICMs from later blastocysts produce endoderm cells. We have found that if embryos are treated with cycloheximide during the transition from the early to late blastocyst stages, subsequently isolated ICMs give rise to trophoblastβlike giant cells. These cells do not, however, exhibit detectable levels of Ξ^5^, 3Ξ²βhydroxysteroid dehydrogenase, an enzyme normally found in primary trophoblast cells. Neither Colcemid nor Ξ±βamanitin affects the conversion of the ICM program in the same way as cycloheximide, although Ξ±βamanitin added at later stages interferes with the formation of a cohesive endoderm layer around the isolated ICM. We propose that the reprogramming of ICM cells involves at least two events: one terminates the giant cell program and the other, occurring later in development, promotes endoderm formation.
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