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Effects of prostaglandin F2? (PGF2?) on cell-death pathways in the bovine corpus luteum (CL).


ABSTRACT: BACKGROUND:Prostaglandin F2? (PGF2?) may differentially affect viability of luteal cells by inducing either proliferation or cell death (via apoptosis or necroptosis). The diverse effects of PGF2? may depend on its local vs. systemic actions. In our study, we determined changes in expression of genes related to: (i) apoptosis: caspase (CASP) 3, CASP8, BCL2 associated X (BAX), B-cell lymphoma 2 (BCL2) and (ii) necroptosis: receptor-interacting protein kinase (RIPK) 1, RIPK3, cylindromatosis (CYLD), and mixed lineage kinase domain-like (MLKL) in the early and mid-stage corpus luteum (CL) that accompany local (intra-CL) vs. systemic (i.m.) analogue of PGF2? (aPGF2?) actions. Cows at day 4 (n?=?24) or day 10 (n?=?24) of the estrous cycle were treated by injections as follows: (1) systemic saline, (2) systemic aPGF2? (25?mg; Dinoprost), (3) local saline, (4) local aPGF2? (2.5?mg; Dinoprost). After 4?h, CLs were collected by ovariectomy. Expression levels of mRNA and protein were investigated by RT-q PCR, Western blotting and immunohistochemistry, respectively. RESULTS:We found that local and systemic administration of aPGF2? in the early-stage CL resulted in decreased expression of CASP3 (P?

SUBMITTER: Jonczyk AW 

PROVIDER: S-EPMC6873574 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature

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Effects of prostaglandin F<sub>2α</sub> (PGF<sub>2α</sub>) on cell-death pathways in the bovine corpus luteum (CL).

Jonczyk Agnieszka Walentyna AW   Piotrowska-Tomala Katarzyna Karolina KK   Skarzynski Dariusz Jan DJ  

BMC veterinary research 20191121 1


<h4>Background</h4>Prostaglandin F<sub>2α</sub> (PGF<sub>2α</sub>) may differentially affect viability of luteal cells by inducing either proliferation or cell death (via apoptosis or necroptosis). The diverse effects of PGF<sub>2α</sub> may depend on its local vs. systemic actions. In our study, we determined changes in expression of genes related to: (i) apoptosis: caspase (CASP) 3, CASP8, BCL2 associated X (BAX), B-cell lymphoma 2 (BCL2) and (ii) necroptosis: receptor-interacting protein kina  ...[more]

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