Frequency and occurrence of late-gestation losses from cattle cloned embryos

被引:303
作者
Heyman, Y [1 ]
Chavatte-Palmer, P
LeBourhis, D
Camous, S
Vignon, X
Renard, JP
机构
[1] INRA, F-78352 Jouy En Josas, France
[2] UNCEIA, Serv Tech, F-94703 Maisons Alfort, France
[3] INRA, F-78352 Jouy En Josas, France
[4] INA PG, F-75231 Paris, France
关键词
assisted reproductive technology; conceptus; embryo; placenta; pregnancy;
D O I
10.1095/biolreprod66.1.6
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nuclear transfer from somatic cells still has limited efficiency in terms of live calves born due to high fetal loss after transfer. In this study, we addressed the type of donor cells used for cloning in in vivo development. We used a combination of repeated ultrasonography and maternal pregnancy serum protein (PSP60) assays to monitor the evolution of pregnancy after somatic cloning in order to detect the occurrence of late-gestation losses and their frequency, compared with embryo cloning or in vitro fertilization (IVF). Incidence of loss between Day 90 of gestation and calving was 43.7% for adult somatic clones and 33.3% for fetal somatic clones, compared with 4.3% after embryo cloning and 0% in the control IVF group. Using PSP60 levels in maternal blood as a criterion for placental function, we observed that after somatic cloning, recipients that lost their pregnancy before Day 100 showed significantly higher PSP60 levels by Day 50 than those that maintained pregnancy (7.77 +/- 3.3 ng/ml vs. 2.45 +/- 0.27 ng/ml for normal pregnancies, P < 0.05). At later stages of gestation, between 4 mo and calving, mean PSP60 concentrations were significantly increased in pathologic pregnancy after somatic cloning compared with other groups (P < 0.05 by Day 150, P < 0.001 by Day 180, and P < 0.01 by Day 210). In those situations, and confirmed by ultrasonographic measurements, recipients developed severe hydroallantois together with larger placentome size. Our findings suggest that assessing placental development with PSP60 and ultrasonography will lead to better care of recipient animals in bovine somatic cloning.
引用
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页码:6 / 13
页数:8
相关论文
共 43 条
[1]   Production of goats by somatic cell nuclear transfer [J].
Baguisi, A ;
Behboodi, E ;
Melican, DT ;
Pollock, JS ;
Destrempes, MM ;
Cammuso, C ;
Williams, JL ;
Nims, SD ;
Porter, CA ;
Midura, P ;
Palacios, MJ ;
Ayres, SL ;
Denniston, RS ;
Hayes, ML ;
Ziomek, CA ;
Meade, HM ;
Godke, RA ;
Gavin, WG ;
Overström, EW ;
Echelard, Y .
NATURE BIOTECHNOLOGY, 1999, 17 (05) :456-461
[2]   In vitro production of embryos alters levels of insulin-like growth factor-II messenger ribonucleic acid in bovine fetuses 63 days after transfer [J].
Blondin, P ;
Farin, PW ;
Crosier, AE ;
Alexander, JE ;
Farin, CE .
BIOLOGY OF REPRODUCTION, 2000, 62 (02) :384-389
[3]  
Chavatte-Palmer P., 2000, Theriogenology, V53, P213
[4]  
CHESNE P, 1993, CR ACAD SCI III-VIE, V316, P487
[5]   Cloned transgenic calves produced from nonquiescent fetal fibroblasts [J].
Cibelli, JB ;
Stice, SL ;
Golueke, PJ ;
Kane, JJ ;
Jerry, J ;
Blackwell, C ;
de Leon, FAP ;
Robl, JM .
SCIENCE, 1998, 280 (5367) :1256-1258
[6]  
Farin P. W., 2001, Theriogenology, V55, P320
[7]   TRANSFER OF BOVINE EMBRYOS PRODUCED IN-VIVO OR IN-VITRO - SURVIVAL AND FETAL DEVELOPMENT [J].
FARIN, PW ;
FARIN, CE .
BIOLOGY OF REPRODUCTION, 1995, 52 (03) :676-682
[8]  
Galli C, 1999, Cloning, V1, P161, DOI 10.1089/15204559950019924
[9]   DEVELOPMENTAL ABILITY OF BOVINE EMBRYOS AFTER NUCLEAR TRANSFER BASED ON THE NUCLEAR SOURCE - IN-VIVO VERSUS IN-VITRO [J].
HEYMAN, Y ;
CHESNE, P ;
LEBOURHIS, D ;
PEYNOT, N ;
RENARD, JP .
THERIOGENOLOGY, 1994, 42 (04) :695-702
[10]  
HEYMAN Y, 1997, P 13 AETE M LYON, P156