Cytoplasmic states of different cytoplast recipients
نویسندگان
چکیده
1359-6004/96 $8.50 Embryo reconstruction by the transfer of a donor nucleus to an enucleated one-cell egg was first proposed by Spemann (1938) to answer the question of nuclear equivalence or ‘Do nuclei change during development?’ By transferring nuclei from increasingly advanced embryonic stages, these experiments were designed to determine at which point the developmental potential of nuclei became restricted. Owing to technical limitations and the unfortunate death of Spemann, these studies were not completed until Briggs and King (1952) demonstrated that certain nuclei could direct development to a sexually mature adult. Their findings led to the current concept that equivalent, totipotent nuclei from a single individual could, when transferred to an enucleated egg, give rise to genetically identical individuals. In the true sense of the meaning, these individuals would not be clones, as unknown cytoplasmic contributions in each may vary and the absence of any chromosomal rearrangements would have to be demonstrated. Since the demonstration of embryo cloning in amphibians, similar techniques have been applied to mammals (see Box 1). The ability to produce genetically identical clones has obvious advantages for research (i.e. as biological controls) and in commercial applications (i.e. uniformity of meat products, animal management). After reconstruction, embryo development depends on many factors, including the ability of the nucleus to direct development, i.e. totipotency, nuclear reprogramming, developmental competence of the recipient cytoplast (i.e. oocyte maturation), oocyte activation and embryo culture (reviewed by Wilmut and Campbell, 1992; Campbell and Wilmut, 1994). Another group of factors can be described as cell cycle effects. Many reports on both amphibians and mammals have shown that the cell cycle stage of both the donor nucleus and the recipient cytoplasm, at the time of transfer, can have substantial effects upon the development of the reconstituted embryo. Cytoplasmic states of different cytoplast recipients
منابع مشابه
P-72: Ovine Oocytes Vitrified at Germinal Vesicle Stage as Cytoplast Recipients forSomatic Cell Nuclear Transfer (SCNT)
Background: The cryopreservation of immature oocytes at the germinal vesicle (GV) stage would create an easily accessible, nonseasonal source of female gametes for research and reproduction. The present study investigated the ability of ovine oocytes vitrified at the GV stage using a cryoloop to be subsequently matured, fertilized and cultured in vitro to blastocyst-stage embryos. Materials and...
متن کاملGerminal vesicle transfer between fresh and cryopreserved immature mouse oocytes.
BACKGROUND We assessed the maturational competence and the chromosomal pattern of mouse oocytes reconstructed by germinal vesicle (GV) transfer technique using nuclear and/or cytoplasmic components from cryopreserved GV stage oocytes. METHODS From 657 GV oocytes (326 fresh and 331 frozen/thawed), four groups of reconstructed oocytes were obtained by micromanipulation and electrofusion: fresh ...
متن کاملMicrotrabecular lattice of the cytoplasmic ground substance. Artifact or reality
The cytoplasmic ground substance of cultured cells prepared for high voltage transmission electron microscopy (glutaraldehyde/osmium fixed, alcohol or acetone dehydrated, critical-point dried) consists of slender (3-6 nm Diam) strands--the microtrabeculae (55)--that form an irregular three-dimensional lattice (the microtrabecular lattice). The microtrabeculae interconnect the membranous and non...
متن کاملMost iodinatable fibroblast surface proteins accompany the cytoplast membrane during cytochalasin B-mediated enucleation of chick embryo fibroblasts
Six different proteins are found to be reproducibly exposed on the cell surface of chicken embryo fibroblasts (CEF) by the criterion of lactoperoxidase-catalyzed iodination (250,000, 185,000, 130,000, 100,000, 87,000, and 75,000 daltons). We wondered whether cell enucleation might lead to a differential partition of these surface proteins with the karyoplast or cytoplast membrane. We found that...
متن کاملImmortalization of human lymphocytes by transfection with DNA from mouse L929 cytoplasts.
Transfection of human peripheral blood lymphocytes with DNA from mouse L929 cytoplasts induced proliferation of lymphocytes and the formation of B and T cell-derived cell lines with apparently unlimited growth potential. The cell lines could be grown in serum-containing media as well as in chemically defined serum-free media, have a nearly normal human karyotype, did not form colonies in soft-a...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 1997