In situ detection of apoptosis in regressing corpus luteum of pregnant sow: Evidence of an early presence of DNA fragmentation

被引:64
作者
Bacci, ML [1 ]
Barazzoni, AM [1 ]
Forni, M [1 ]
Costerbosa, GL [1 ]
机构
[1] UNIV BOLOGNA,DEPT VET MORPHOL & PHYSIOL & ANIM PROD,BOLOGNA,ITALY
关键词
D O I
10.1016/0739-7240(96)00049-5
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Luteolysis has been shown to be correlated with apoptosis in rats, sheep, and cows. In pigs, apoptosis has already been demonstrated as regards atretic follicles. The present study has been conducted to evaluate whether apoptosis occurs during corpora lutea regression in the pregnant pig and to investigate the temporal relationship between apoptosis and functional luteolysis. The apoptotic process has been studied through the research of oligonucleosome fragmentation by means of classical electrophoresis methods and by in situ detection on histological luteal sections. The latter method allows the identification of apoptosis and the localization of apoptotic cells. Pregnant sows were cloprostenol (PGF(2 alpha) analog) treated and ovariectomized 0, 6, 12, 24, 48, and 72 hr after treatment. Corpora lutea were utilized for progesterone and DNA extraction and in situ evaluation of apoptosis. Clear evidence of apoptosis was seen earlier with the in situ technique (6 hr for stromal tissue, 12 hr for luteal cells) than with the classical method (24 hr). Apoptosis was, however, apparent after plasma and tissue progesterone had reached basal levels. In conclusion, these results are consistent with the hypothesis that apoptosis occurs during luteolysis in pigs. Moreover, the data obtained with the in situ technique made it possible to identify signs of structural regression in stromal tissue first than in parenchymal cells. A two-stage activation of apoptosis has been discussed to explain structural changes that occur during luteolysis after cloprostenol treatment in swine corpora lutea.
引用
收藏
页码:361 / 372
页数:12
相关论文
共 47 条
[1]  
ANDERSEN J, 1926, CONTRIB EMBRYOL CARN, V17, P107
[2]  
ANDERSON L. L., 1967, P285
[3]  
ARENDS MJ, 1990, AM J PATHOL, V136, P593
[4]  
AZMI TI, 1984, LAB INVEST, V51, P206
[5]  
BABBS CF, 1991, AM J PATHOL, V139, P1069
[6]  
BACCI ML, 1996, IN PRESS P 14 INT PI
[7]  
Behrman H.R., 1993, REPROD MED REV, V2, P153, DOI 10.1017/S0962279900000697
[8]  
Belt W. D, 1970, Biology Reprod., V2, P98, DOI 10.1095/biolreprod2.1.98
[9]   MECHANISMS OF ISCHEMIC ACUTE-RENAL-FAILURE [J].
BONVENTRE, JV .
KIDNEY INTERNATIONAL, 1993, 43 (05) :1160-1178
[10]   DECLINE IN FLUORESCENT LOW-DENSITY-LIPOPROTEIN (LDL) UPTAKE BY SMALL AND LARGE PORCINE LUTEAL CELLS WITH ADVANCING AGE OF THE CORPUS-LUTEUM [J].
BRANNIAN, JD ;
KURZ, SG ;
SHIIGI, SM .
BIOLOGY OF REPRODUCTION, 1994, 50 (01) :204-209