## Abstract Short, hairpin RNA (shRNA) directed against bone morphogenetic protein 4 (Bmpβ4) was delivered to early postimplantation staged mouse embryos via tail vein injection of pregnant dams. As early as 24 h postinjection, embryos expressed a DsRed marker and later exhibited defects of neural
Inhibition of early postimplantation development of cultured mouse embryos by bromodeoxyuridine
β Scribed by Spindle, Akiko I.
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 1005 KB
- Volume
- 202
- Category
- Article
- ISSN
- 0022-104X
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Mouse embryos were treated with 5βbromodeoxyuridine (BrdUrd) for 24 hours at various preimplantation stages to determine its effect on early postimplantation development. The inhibitory effect of BrdUrd (10^β7^ to 10^β6^ M) on trophoblast outgrowth and inner cell mass (ICM) development was least severe when embryos were treated at the 2βcell stage and was most severe when they were treated at the morula stage. When embryos were treated at the blastocyst stage, the inhibitory effect on trophoblast outgrowth decreased, but that on ICM development remained severe. The severity of inhibition, particularly that on ICM development, appeared to be related to decreased cell numbers in BrdUrdβtreated embryos. However, increasing the cell number by aggregating two ICM's isolated from BrdUrdβtreated blastocysts did not increase their chance of survival or of forming two primary germ layers. This indicates that the decrease in cell numbers alone is not the cause of the failure of BrdUrdβtreated embryos to develop.
The mechanism of BrdUrd inhibition was studied by adding thymidine or deoxycytidine during BrdUrd treatments. A 10βfold excess of thymidine completely protected embryos from the inhibitory effect of BrdUrd. A 10βfold excess of deoxycytidine was less effective. Autoradiography indicated that both thymidine and deoxycytidine protected embryos by interfering with the incorporation of BrdUrd into the DNA.
π SIMILAR VOLUMES
## Abstract Preimplantation embryos from matings between yellow heterozygous (A^y^/a) mice were recovered at 56 hours __post coitum__, cultured for five days, and compared with the development of embryos from three control matings (A^y^/a β Γ a/a β, a/a β Γ A^y^/a β, a/a β Γ a/a β). Most embryos we
## Abstract We have compared the in vitro development of 8.5βday early somitic mouse embryos cultured in static organ culture dishes in human cord serum or rat serum with the development of embryos of the same age cultured in rotating tubes or developing in vivo. The growth of embryos cultured in r
A rotator whole embryo culture system was used to assess the growth and development of late-primitive-streak-stage (Theiler stage 9-10) mouse embryos to the limb-bud stage of organogenesis in a variety of media containing combinations of mouse serum (MS), rat serum (RS), and Tyrode's buffer (TB). Th
## Abstract Summary: This study reports establishment of an in vitro culture system for E5.5 mouse embryos that supports development to the gastrulation stage and allows the use of experimental approaches to study gastrulation during mouse embryogenesis. Recent experiments suggest that the extraemb