Ovaries were surgically removed from female goats (Toggenburg, Nubian
and Saanen breeds). Oocytes were collected by follicular aspiration or
after ovaries were minced, then matured in mTCM-199 with 100 mu g LH
+ 0.5 mu g FSH + 1.0 mu g estradiol 17-beta/ml for 27 h prior to in vi
tro fertilization (17). Although more oocytes were made available by m
incing than by aspiration, higher proportions of aspirated oocytes wer
e fertilized and developed to morulae. Proportions that fertilized and
reached morulae were 82/102 (80.4%) and 50/102 (49.0%) versus 77/126
(61.1%) and 27/126 (21.4%) for oocytes obtained by aspiration and afte
r ovarian mincing, respectively (P<0.05). Proportions of inseminated o
va undergoing cleavage and continuing development to the morula stage
differed significantly (P<0.05) among 5 co-culture treatment groups, w
ith higher proportions of cleavage (23/27, 85.2%) and morulae (14/27,
51.9%) obtained by co-culture on caprine cumulus cells (cCC). Some ooc
ytes reached the blastocyst stage (4/54, 7.4%) following oocyte collec
tion by aspiration and culture on caprine oviduct epithelial cells (cO
EC). After 4- and 8-cell stage embryos obtained by aspiration and cult
ure on cCC were transferred pregnancy resulted. Twin male kids (develo
ped from different embryos) were born on August 6, 1993, and have deve
loped into normal bucks. Conditions reported here provided an adequate
environment for support of oocyte maturation, fertilization and early
embryonic development in vitro (IVMFC) with normal development after
embryo transfer.