TY - JOUR
T1 - Targeting αgal epitopes for multi-species embryo immunosurgery
AU - Kurome, Mayuko
AU - Baehr, Andrea
AU - Simmet, Kilian
AU - Jemiller, Eva Maria
AU - Egerer, Stefanie
AU - Dahlhoff, Maik
AU - Zakhartchenko, Valeri
AU - Nagashima, Hiroshi
AU - Klymiuk, Nikolai
AU - Kessler, Barbara
AU - Wolf, Eckhard
N1 - Publisher Copyright:
© 2019 CSIRO.
PY - 2019
Y1 - 2019
N2 - Immunosurgical isolation of the inner cell mass (ICM) from blastocysts is based on complement-mediated lysis of antibody-coated trophectoderm (TE) cells. Conventionally, anti-species antisera, containing antibodies against multiple undefined TE-cell epitopes, have been used as the antibody source. We previously generated α-1,3-galactosyltransferase deficient (GTKO) pigs to prevent hyperacute rejection of pig-to-primate xenotransplants. Since GTKO pigs lack galactosyl-α-1,3-galactose (αGal) but are exposed to this antigen (e.g. αGal on gut bacteria), they produce anti-αGal antibodies. In this study, we examined whether serum from GTKO pigs could be used as a novel antibody source for multi-species embryo immunosurgery. Mouse, rabbit, pig and cattle blastocysts were used for the experiment. Expression of αGal epitopes on the surface of TE cells was detected in blastocysts of all species tested. GTKO pig serum contained sufficient anti-αGal antibodies to induce complement-mediated lysis of TE cells in blastocysts from all species investigated. Intact ICMs could be successfully recovered and the majority showed the desired level of purity. Our study demonstrates that GTKO pig serum is a reliable and effective source of antibodies targeting the αGal epitopes of TE cells for multi-species embryo immunosurgery.
AB - Immunosurgical isolation of the inner cell mass (ICM) from blastocysts is based on complement-mediated lysis of antibody-coated trophectoderm (TE) cells. Conventionally, anti-species antisera, containing antibodies against multiple undefined TE-cell epitopes, have been used as the antibody source. We previously generated α-1,3-galactosyltransferase deficient (GTKO) pigs to prevent hyperacute rejection of pig-to-primate xenotransplants. Since GTKO pigs lack galactosyl-α-1,3-galactose (αGal) but are exposed to this antigen (e.g. αGal on gut bacteria), they produce anti-αGal antibodies. In this study, we examined whether serum from GTKO pigs could be used as a novel antibody source for multi-species embryo immunosurgery. Mouse, rabbit, pig and cattle blastocysts were used for the experiment. Expression of αGal epitopes on the surface of TE cells was detected in blastocysts of all species tested. GTKO pig serum contained sufficient anti-αGal antibodies to induce complement-mediated lysis of TE cells in blastocysts from all species investigated. Intact ICMs could be successfully recovered and the majority showed the desired level of purity. Our study demonstrates that GTKO pig serum is a reliable and effective source of antibodies targeting the αGal epitopes of TE cells for multi-species embryo immunosurgery.
KW - 3-galactosyltransferase deficient pigs
KW - anti-αGal antibodies
KW - complement
KW - inner cell mass isolation
KW - α-1
UR - http://www.scopus.com/inward/record.url?scp=85056106314&partnerID=8YFLogxK
U2 - 10.1071/RD18120
DO - 10.1071/RD18120
M3 - Article
C2 - 30384878
AN - SCOPUS:85056106314
SN - 1031-3613
VL - 31
SP - 820
EP - 826
JO - Reproduction, Fertility and Development
JF - Reproduction, Fertility and Development
IS - 4
ER -