Literature DB >> 1702069

Antibodies to a renal Na+/glucose cotransport system localize to the apical plasma membrane domain of polar mouse embryo blastomeres.

L M Wiley1, J E Lever, C Pape, G M Kidder.   

Abstract

Mouse preimplantation embryos were examined for the cell surface expression of epitopes that cross-react with antibodies to a 75-kDa subunit of a purified porcine renal brush border Na+/glucose cotransport system. A Na+ cotransport system is hypothesized to reside in the apical plasma membrane domain of mouse polar blastomeres and to be associated with the induction of their apical-basal polarity. Western blot analysis showed that unfertilized oocytes as well as preimplantation embryos contain a cross-reacting antigen with an apparent molecular weight of about 75,000. Embryos and their isolated blastomeres were double-labeled and assayed by indirect immunofluorescence (IIF) for the expression of epitopes (visualized by labeling with rabbit antiserum or mouse monoclonal IgG to cotransporter followed by the appropriate rhodamine-conjugated second antibodies) and for the development of cell surface polarity (visualized by the apical restriction of fluoresceinated succinylated concanavalin A binding; FS Con A). IIF did not detect these epitopes until after the second cleavage when 4-cell embryos expressed low-to-moderate levels. Although epitopes were expressed on all surfaces of 4-cell blastomeres, some blastomeres expressed more epitopes on their apical surfaces than on their basolateral ones. All precompaction 8-cell embryos expressed epitopes, with expression being greater apically on some blastomeres. The level of expression appeared to reach a maximum on morulae and to decline on cavitating embryos. Assays performed on isolated blastomeres from postcompaction embryos showed that by the 16-cell stage epitope expression appeared to become restricted to FS Con A-labeled apical plasma membrane domains and was no longer evident on basolateral domains. This apparent apical restriction of epitope expression was confirmed by electron microscopic examination of immunogold-labeled isolated polar 16-cell blastomeres. These results demonstrate that preimplantation mouse embryos contain an antigen(s) that is immunologically and structurally similar to a 75-kDa renal Na+/glucose cotransporter. The onset of cell surface expression of this antigen precedes development of the stable polar phenotype.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1702069     DOI: 10.1016/0012-1606(91)90062-8

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  4 in total

Review 1.  Metabolic and therapeutic lessons from genetic manipulation of GLUT4.

Authors:  M J Charron; E B Katz
Journal:  Mol Cell Biochem       Date:  1998-05       Impact factor: 3.396

2.  Ion transport across the early chick embryo: II. Characterization and pH sensitivity of the transembryonic short-circuit current.

Authors:  H Abriel; U Katz; P Kucera
Journal:  J Membr Biol       Date:  1994-08       Impact factor: 1.843

3.  An unusual active hexose transport system in human and mouse preimplantation embryos.

Authors:  M M Chi; J K Manchester; R Basuray; S Mahendra; R C Strickler; D B McDougal; O H Lowry
Journal:  Proc Natl Acad Sci U S A       Date:  1993-11-01       Impact factor: 11.205

Review 4.  Glucose transporters in gametes and preimplantation embryos.

Authors:  Scott H Purcell; Kelle H Moley
Journal:  Trends Endocrinol Metab       Date:  2009-10-05       Impact factor: 12.015

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.