Beneficial effects of Vero cells for developing IVF bovine eggs in two different coculture systems

被引:43
作者
Menck, MC
GuyaderJoly, C
Peynot, N
LeBourhis, D
Lobo, RB
Renard, JP
Heyman, Y
机构
[1] INRA,UNITE BIOL DEV,F-78352 JOUY EN JOSAS,FRANCE
[2] UNCEIA,SERV TECH,F-94703 MAISONS ALFORT,FRANCE
[3] UNIV SAO PAULO,FAC MED RIBEIRAO PRETO,RIBEIRAO PRET,SP,BRAZIL
来源
REPRODUCTION NUTRITION DEVELOPMENT | 1997年 / 37卷 / 02期
关键词
bovine; embryo; coculture; IVF; blastocyst;
D O I
10.1051/rnd:19970202
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
A Vero cell line was used for coculture of bovine in vitro fertilized eggs up to blastocyst stage in comparison with bovine oviductal epithelial cells (BOEC) in two culture systems: monolayers or microdrops. Inseminated oocytes cocultured for 7 days with Vero cells in microdrops resulted in a significantly higher blastocyst rate compared to BOEC (29.5% vs 21.1%, respectively; P < 0.01). This difference was not significant in the monolayer coculture system although the blastocyst rate tended to be higher with Vero than with BOEC monolayers (27% vs 22.3%, respectively). Interestingly, the coefficient of variation between replicates was lower in both Vero cell groups than in BOEC groups indicating that Vero cells may help reduce variability. Medium conditioned by Vero cells partly supported embryo development compared to coculture itself (14.6% vs 26.5%, respectively; P < 0.01). Blastocysts developed on Vero cells contained significantly more cells (142 +/- 39) than those developed on BOEC (88.8 +/- 32.8, P < 0.001). Viability of blastocysts developed on Vero cells was evaluated by single transfer to 26 recipient heifers. Confirmed pregnancy rate after 3 months was 58%, demonstrating their high viability.
引用
收藏
页码:141 / 150
页数:10
相关论文
共 34 条
[11]  
GANDOLFI F, 1987, J REPROD FERTIL, V81, P23, DOI 10.1530/jrf.0.0810023
[12]   ENHANCED RATES OF CLEAVAGE AND DEVELOPMENT FOR SHEEP ZYGOTES CULTURED TO THE BLASTOCYST STAGE IN-VITRO IN THE ABSENCE OF SERUM AND SOMATIC-CELLS - AMINO-ACIDS, VITAMINS, AND CULTURING EMBRYOS IN GROUPS STIMULATE DEVELOPMENT [J].
GARDNER, DK ;
LANE, M ;
SPITZER, A ;
BATT, PA .
BIOLOGY OF REPRODUCTION, 1994, 50 (02) :390-400
[13]  
Hasler J.F., 1996, BIOL REPROD S1, V54, P89
[14]   Cellular evaluation of bovine nuclear transfer embryos developed in vitro [J].
Heyman, Y ;
Degrolard, J ;
Adenot, P ;
Chesne, P ;
Flechon, B ;
Renard, JP ;
Flechon, JE .
REPRODUCTION NUTRITION DEVELOPMENT, 1995, 35 (06) :713-723
[15]  
HEYMAN Y, 1987, MAMMALIAN PREIMPLANT, P175
[16]  
KAJIHARA Y, 1987, Japanese Journal of Animal Reproduction, V33, P173
[17]   THE ROLE OF NUTRIENTS, PEPTIDE GROWTH-FACTORS AND COCULTURE CELLS IN DEVELOPMENT OF PREIMPLANTATION EMBRYOS INVITRO [J].
KANE, MT ;
CARNEY, EW ;
ELLINGTON, JE .
THERIOGENOLOGY, 1992, 38 (02) :297-313
[18]   BLASTOCYST EXPANSION, HATCHING, AND ATTACHMENT OF PORCINE EMBRYOS COCULTURED WITH BOVINE FIBROBLASTS INVITRO [J].
KUZAN, FB ;
WRIGHT, RW .
ANIMAL REPRODUCTION SCIENCE, 1982, 5 (01) :57-63
[19]   In vitro development of bovine embryos in conditioned media from bovine granulosa cells and Vero cells cultured in exogenous protein- and amino acid-free chemically defined human tubal fluid medium [J].
Maeda, J ;
Kotsuji, F ;
Negami, A ;
Kamitani, N ;
Tominaga, T .
BIOLOGY OF REPRODUCTION, 1996, 54 (04) :930-936
[20]   INVITRO CULTURE OF BOVINE EGG FERTILIZED EITHER INVIVO OR INVITRO [J].
MARQUANTLEGUIENNE, B ;
GERARD, M ;
SOLARI, A ;
THIBAULT, C .
REPRODUCTION NUTRITION DEVELOPMENT, 1989, 29 (05) :559-568