Display options
Cite
Menino AR, Williams JS, Gardiner CS. Development of mouse embryos in media containing lectins. Theriogenology. 1989;31(4):821-34doi: 10.1016/0093-691x(89)90027-7.
Menino, A. R., Williams, J. S., & Gardiner, C. S. (1989). Development of mouse embryos in media containing lectins. Theriogenology, 31(4), 821-34. https://doi.org/10.1016/0093-691x(89)90027-7
Menino, A R, et al. "Development of mouse embryos in media containing lectins." Theriogenology vol. 31,4 (1989): 821-34. doi: https://doi.org/10.1016/0093-691x(89)90027-7
Menino AR, Williams JS, Gardiner CS. Development of mouse embryos in media containing lectins. Theriogenology. 1989 Apr;31(4):821-34. doi: 10.1016/0093-691x(89)90027-7. PMID: 16726597.
Copy Download .nbib Format: NLM
Share it on

Theriogenology. 1989 Apr;31(4):821-34. doi: 10.1016/0093-691x(89)90027-7.

Development of mouse embryos in media containing lectins.

Theriogenology

A R Menino, J S Williams, C S Gardiner

Affiliations

  1. Department of Animal Science Oregon State University Corvallis, OR 97331-6702 USA.

PMID: 16726597 DOI: 10.1016/0093-691x(89)90027-7

Abstract

Lectins known to stimulate mitosis in cultured cells were evaluated for effects on development of mouse embryos in vitro. Two-cell mouse embryos were cultured in one of the following treatments: Whitten's medium as the control medium; Whitten's medium with 1, 10 or 100 mug/ml concanavalin A; Whitten's medium with 1, 10 or 100 mug/ml leucoagglutinin; Whitten's medium with 1, 10 or 100 mug/ml phytohemagglutinin; Whitten's medium with 1, 10 or 100 mug/ml pokeweed-mitogen; and Whitten's medium with 1, 10 or 100 mug/ml wheat germ agglutinin. Development to the morula stage was blocked in media with 100 mug/ml concanavalin A and 10 and 100 mug/ml wheat germ agglutinin, whereas blastocyst formation was blocked in all pokeweed-mitogen supplemented media. Embryos incubated in 10 and 100 mug/ml wheat germ agglutinin underwent premature cavitation or vacuolation at 24 to 48 h of culture. More embryos formed blastocysts in media with 1 and 100 mug/ml phytohemagglutinin and 10 mug/ml leucoagglutinin than in Whitten's medium (P<0.05). The percentage of embryos hatching was greatest in 1 mug/ml phytohemagglutinin (P<0.05), but it was the same in Whitten's medium, 1 mug/ml concanavalin A and 1 mug/ml leucoagglutinin (P>0.05). Cell division was not stimulated by the lectins; however, it was significantly suppressed in media with 10 and 100 mug/ml concanavalin A, 100 mug/ml phytohemagglutinin, 1, 10 and 100 mug/ml pokeweed-mitogen, and 10 and 100 mug/ml wheat germ agglutinin. Solubility of the zona pellucida in sodium isothicyanate (NaSCN) was reduced in 100 mug/ml phytohemagglutinin, 100 mug/ml leucoagglutinin and 1 mug/ml wheat germ agglutinin media (P<0.05) when compared to Whitten's medium and may have accounted for the reduced hatching observed in these treatments. Development of isolated blastomeres into blastocysts was reduced in media with 1 mug/ml wheat germ agglutinin, 1 mug/ml concanavalin A, and 10 and 100 mug/ml leucoagglutinin (P<0.05) but was similar in media with 1 mug/ml leucoagglutinin and 1, 10 and 100 mug/ml phytohemagglutinin when compared to Whitten's medium (P>0.05). The extent of embryo development in media with lectins depended upon the degree of cytotoxicity and potential biochemical modifications induced in the zona pellucida. Greatest embryo development took place in medium with 1 mug/ml phytohemagglutinin; however, the mechanism was not that of stimulation of cell division or a change in zona pellucida solubility.

Publication Types