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Biomedical subjects

William A Ritchie

Publications and source records attributed to William A Ritchie.

4 recordsLinked to original sources

Nuclear transfer in sheep.

Somatic cell nuclear transfer is a complex and intricate procedure with a low success rate. Despite advances in embryo culture and the production of specialized tools and equipment success rate has remained poor. The procedure remains basically the same despite technical innovations but is now easier to learn and requires less technical expertise. Oocytes now come from an in vitro system, which may make the procedure more economical and flexible than before. Oocytes are produced from ovaries collected at an abattoir. The cumulus oocyte complexes (COCs) are recovered from the ovary with hypodermic needle and syringe. Selected COCs are matured for 18 to 20 h in medium that is supplemented with hormones. Cumulus cells are stripped from the oocytes using hyaluronidase, and mature oocytes with polar bodies, selected for enucleation. These oocytes are treated with a cytoskelatal inhibitor to prevent lysis of the oocyte during enucleation and with a DNA-specific dye to visualize the chromosomes with the aid of ultraviolet light. These permit removal of the metaphase II chromosomes and polar body prior to reconstruction of the embryo. A diploid cell is injected under the zona pellucida of the enucleated oocyte, which can then be fused to the cytoplast using an electrical pulse. The fused embryos are activated and allowed to develop in culture to the morula or blastocyst stage, when they are surgically implanted into previously prepared synchronized, recipient animals.

Active Transport, Cell Nucleus↗

Live lambs born from zona-pellucida denuded embryos.

Progress with techniques using zona-pellucida denuded embryos has resulted in the birth of live cattle, pigs, and mice. The application of zona-free methods in sheep has been restricted to in vitro studies. In this report, we demonstrate that live lambs can be produced from zona-free IVF embryos. We are pursuing this method as a prerequisite to developing viral vector co-culture delivery strategies.

Animals↗

Efficient generation of transgenic pigs using equine infectious anaemia virus (EIAV) derived vector.

Traditional methods of transgene delivery in livestock are inefficient. Recently, human immunodeficiency virus (HIV-1) based lentiviral vectors have been shown to offer an efficient transgene delivery system. We now extend this method by demonstrating efficient generation of transgenic pigs using an equine infectious anaemia virus derived vector. We used this vector to deliver a green fluorescent protein expressing transgene; 31% of injected/transferred eggs resulted in a transgenic founder animal and 95% of founder animals displayed green fluorescence. This compares favourably with results using HIV-1 based vectors, and is substantially more efficient than the standard pronuclear microinjection method, indicating that lentiviral transgene delivery may be a general tool with which to efficiently generate transgenic mammals.

Animals↗

Somatic cell nuclear transfer in the pig: control of pronuclear formation and integration with improved methods for activation and maintenance of pregnancy.

To clone a pig from somatic cells, we first validated an electrical activation method for use on ovulated oocytes. We then evaluated delayed versus simultaneous activation (DA vs. SA) strategies, the use of 2 nuclear donor cells, and the use of cytoskeletal inhibitors during nuclear transfer. Using enucleated ovulated oocytes as cytoplasts for fetal fibroblast nuclei and transferring cloned embryos into a recipient within 2 h of activation, a 2-h delay between electrical fusion and activation yielded blastocysts more reliably and with a higher nuclear count than did SA. Comparable rates of development using DA were obtained following culture of embryos cloned from ovulated or in vitro-matured cytoplasts and fibroblast or cumulus nuclei. Treatment of cloned embryos with cytochalasin B (CB) postfusion and for 6 h after DA had no impact on blastocyst development as compared with CB treatment postfusion only. Inclusion of a microtubule inhibitor such as nocodozole with CB before and after DA improved nuclear retention and favored the formation of single pronuclei in experiments using a membrane dye to reliably monitor fusion. However, no improvement in blastocyst development was observed. Using fetal fibroblasts as nuclear donor cells, a live cloned piglet was produced in a pregnancy that was maintained by cotransfer of parthenogenetic embryos.

Animals↗