Title of article :
Delayed parturition in cloned calves associated with persistently elevated placentomal TGF-β1 expression
Author/Authors :
Hwang، نويسنده , , Seongsoo and Chang، نويسنده , , Yoo-Min and Ko، نويسنده , , Yeoung-Gyu and Yang، نويسنده , , Byoung-Chul and Min، نويسنده , , Kwan-Sik and Yoon، نويسنده , , Jong-Taek and Nho، نويسنده , , Whan-Gook and Kim، نويسنده , , Chang-Keun and Seong، نويسنده , , Hwan-Hoo and Kim، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2009
Pages :
6
From page :
290
To page :
295
Abstract :
The objective of this study was to investigate hormonal and TGF-β1 characterizations of delayed parturition in the SCNT recipients (Korean native beef cattle: Hanwoo). The SCNT blastocysts produced by Hanwoo fetal fibroblast cells were transferred into the synchronized Hanwoo recipients. The artificially inseminated Hanwoo recipients (AI-R) were used as control. All AI-R were labored by natural delivery. The SCNT recipients (SCNT-R) with no signs of delivery were operated by Caesarean section. The blood and placentomes were collected during parturition. The weight of placentomes in SCNT-R (n = 12, 301 ± 41.22 g) was significantly higher than that of AI-R (n = 10, 204.8 ± 24.89 g) (p < 0.05). There were significantly lower E2 (p < 0.05) or higher P4 (p < 0.01) and TGF-β1 (p < 0.01) levels in the SCNT-R compared to that of AI-R, respectively. The SCNT-R showed a higher placentomal TGF-β1 protein level compared to that of AI-R (p < 0.01). Interestingly, the TGF-β1 protein level in SCNT-R with normal delivery was dramatically decreased as same as AI-R, but it was highly maintained in C-sec at days 250 of pregnancy in AI-R. These results suggest that delayed parturition in clone calving may be associated with persistence of elevated TGF-beta-1 expression in late pregnancy.
Keywords :
Delayed parturition , hormones , Placentome , TGF-?1 , Clone calving
Journal title :
Animal Reproduction Science
Serial Year :
2009
Journal title :
Animal Reproduction Science
Record number :
1910750
Link To Document :
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