Accumulation of caspase-3 messenger ribonucleic acid and induction of caspase activity in the ovine corpus luteum following prostaglandin F-2 alpha treatment in vivo

Citation
Br. Rueda et al., Accumulation of caspase-3 messenger ribonucleic acid and induction of caspase activity in the ovine corpus luteum following prostaglandin F-2 alpha treatment in vivo, BIOL REPROD, 60(5), 1999, pp. 1087-1092
Citations number
52
Categorie Soggetti
da verificare
Journal title
BIOLOGY OF REPRODUCTION
ISSN journal
00063363 → ACNP
Volume
60
Issue
5
Year of publication
1999
Pages
1087 - 1092
Database
ISI
SICI code
0006-3363(199905)60:5<1087:AOCMRA>2.0.ZU;2-1
Abstract
Caspase-3, a vertebrate homologue of the protein encoded by the Caenorhabdi tis elegans cell death gene, ced-3, induces apoptosis when overexpressed in eukaryotic cells, Since apoptosis occurs during corpus luteum (CL) regress ion in many species, including the ewe, these studies were conducted to 1) isolate a cDNA encoding ovine caspase-3, 2) measure steady state amounts of caspase-3 mRNA in the CL during luteolysis induced by prostaglandin F-2 al pha (PGF(2 alpha)) and during the time of maternal recognition of pregnancy , and 3) measure changes in caspase activity during PGF(2 alpha)-initiated luteal regression. Oligonucleotide primers corresponding to a human caspase -3 cDNA sequence were combined with total RNA from ovine CL in a reverse tr anscription-polymerase chain reaction-based procedure to amplify a 640-base pair partial cDNA with a nucleotide sequence 86% and 81% identical to the human and rat caspase-3 cDNAs, respectively. CL were collected from ewes at 0, 12, or 24 h after treatment with PGF(2 alpha) on Day 10 of the estrous cycle and from nonpregnant and pregnant ewes on Day 12 or Day 14 of the cyc le. Northern blot analysis of total cellular RNA from ovine CL and a radiol abeled ovine caspase-3 cRNA probe indicated the presence of a single mRNA t ranscript of approximately 2.5 kilobases. Levels of caspase-3 mRNA were app roximately 3-fold higher (p < 0.05) in CL at 12 h and 24 h after PGF(2 alph a) in comparison to those levels measured in matched CL from untreated ewes . There were no differences (p > 0.05) in amounts of caspase-3 mRNA in CL o n Day 12 or Day 14 of the estrous cycle compared to Day 12 or Day 14 of pre gnancy, respectively. Caspase activity in CL (measured by the ability of CL lysates to cleave an artificial caspase substrate) was also significantly (p < 0.05) increased in CL collected after treatment with PGF(2 alpha) comp ared to CL collected from nontreated ewes, We conclude that physiological c ell death during PGF(2 alpha)-induced luteal regression in the ewe is media ted, at least in part, via increased expression and activity of the caspase family of pro-apoptotic proteases.