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Biology of reproduction2010; 83(6); 901-908; doi: 10.1095/biolreprod.110.084699

Is FAS/Fas ligand system involved in equine corpus luteum functional regression?

Abstract: Proapoptotic factor Fas ligand (FASL) and its cell surface receptor FAS are tumor necrosis factor superfamily members that trigger apoptosis in different cell types. However, their influence on luteal steroidogenesis is not clearly understood. The aim of the present work was to determine (i) the presence of the cytokine FASL and its receptor FAS in the mare's corpus luteum (CL) throughout the luteal phase, as well as (ii) the influence of FASL alone, or together with the cytokines tumor necrosis factor alpha (TNF) and interferon gamma (IFNG), on equine luteal cell production of luteotrophic and luteolytic factors, cell viability, and apoptosis. FASL and FAS protein expression and mRNA transcription were evaluated in different luteal stages of the equine CL by Western blotting and real-time PCR assays, respectively. Protein expression and FASL mRNA transcription increased in the late CL. Also, FAS and FASL proteins were present in large steroidogenic and endothelial CL cells throughout the luteal phase, as demonstrated by immunohistochemistry. Equine luteal cells isolated from midluteal phase CL were stimulated without (control) or with exogenous cytokines: FASL (10 ng/ml); TNF+IFNG (10 ng/ml each; positive control) or FASL+TNF+IFNG (10 ng/ml each). FASL clearly inhibited in vitro progesterone and prostaglandin E(2) (PGE(2)) production by equine luteal cells but increased prostaglandin F(2alpha) (PGF(2alpha)). Furthermore, FASL effect on equine luteal cell viability depended on the presence of cytokines TNF and IFNG. In conclusion, this study shows the presence of FASL and FAS in the equine CL and suggests their importance in functional luteolysis.
Publication Date: 2010-08-18 PubMed ID: 20720169DOI: 10.1095/biolreprod.110.084699Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Validation Study

Summary

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The research article explores the role of Fas ligand (FASL) and its receptor FAS in the functional regression of the corpus luteum in horses. It specifically investigates their presence in the corpus luteum throughout the luteal phase and their influence on the production of luteotrophic and luteolytic factors, cell viability, and apoptosis.

Research Objectives and Methods

  • The main aim of this study was to find out if FASL and FAS, proapoptotic factors from the tumor necrosis factor superfamily, are present in the mare’s corpus luteum during the luteal phase. This was measured through Western blotting and real-time PCR assays.
  • The secondary goal was to identify the influence of FASL singly, or alongside cytokines such as tumor necrosis factor alpha (TNF) and interferon gamma (IFNG), on the equine cell production of luteotrophic (maintenance of the corpus luteum) and luteolytic factors (trigger the degradation of the corpus luteum), cell viability and apoptosis.

Key Findings

  • The presence of FASL and FAS were established in the equine corpus luteum in all stages of the luteal phase.
  • The presence of FASL and FAS were particularly noticeable in large steroidogenic and endothelial CL cells throughout the luteal phase, as shown by immunohistochemistry.
  • FASL had a significant impact on the in vitro production of progesterone and prostaglandin E(2) (PGE(2)) by equine luteal cells, and also increased the production of prostaglandin F(2alpha) (PGF(2alpha)). Additionally, the impact of FASL on cell viability was dependent on the presence of TNF and IFNG, reinforcing their interconnected influence on cell behavior.

Conclusion

  • The study demonstrates the presence of FASL and FAS in the corpus luteum of horses and suggests their important role in the process of functional luteolysis, the degradation of the corpus luteum. This indicates that these proteins might contribute to the regulation of the reproductive cycle in mares.

Cite This Article

APA
Galvao AM, Ramilo DW, Skarzynski DJ, Lukasik K, Tramontano A, Mollo A, Mateus LM, Ferreira-Dias GM. (2010). Is FAS/Fas ligand system involved in equine corpus luteum functional regression? Biol Reprod, 83(6), 901-908. https://doi.org/10.1095/biolreprod.110.084699

Publication

ISSN: 1529-7268
NlmUniqueID: 0207224
Country: United States
Language: English
Volume: 83
Issue: 6
Pages: 901-908

Researcher Affiliations

Galvao, Antonio M
  • C.I.I.S.A., Faculty of Veterinary Medicine, Technical University of Lisbon, Lisbon, Portugal.
Ramilo, David W
    Skarzynski, Dariusz J
      Lukasik, Karolina
        Tramontano, Angela
          Mollo, Antonio
            Mateus, Luisa M
              Ferreira-Dias, Graca Maria L

                MeSH Terms

                • Animals
                • Apoptosis
                • Cell Survival
                • Cells, Cultured
                • Corpus Luteum / cytology
                • Corpus Luteum / metabolism
                • Dinoprost / metabolism
                • Dinoprostone / metabolism
                • Fas Ligand Protein / genetics
                • Fas Ligand Protein / metabolism
                • Female
                • Gene Expression Regulation
                • Horses
                • Immunohistochemistry
                • Interferon-gamma / metabolism
                • Luteal Phase / metabolism
                • Luteolysis / metabolism
                • Progesterone / metabolism
                • RNA, Messenger / metabolism
                • Signal Transduction
                • Tumor Necrosis Factor-alpha / metabolism
                • fas Receptor / genetics
                • fas Receptor / metabolism

                Citations

                This article has been cited 7 times.
                1. Rebordão MR, Amaral A, Fernandes C, Silva E, Lukasik K, Szóstek-Mioduchowska A, Pinto-Bravo P, Galvão A, Skarzynski DJ, Ferreira-Dias G. Enzymes Present in Neutrophil Extracellular Traps May Stimulate the Fibrogenic PGF(2α) Pathway in the Mare Endometrium.. Animals (Basel) 2021 Sep 6;11(9).
                  doi: 10.3390/ani11092615pubmed: 34573581google scholar: lookup
                2. Walewska E, Wołodko K, Skarzynski D, Ferreira-Dias G, Galvão A. The Interaction Between Nodal, Hypoxia-Inducible Factor 1 Alpha, and Thrombospondin 1 Promotes Luteolysis in Equine Corpus Luteum.. Front Endocrinol (Lausanne) 2019;10:667.
                  doi: 10.3389/fendo.2019.00667pubmed: 31632347google scholar: lookup
                3. Amelkina O, Zschockelt L, Painer J, Serra R, Villaespesa F, Braun BC, Jewgenow K. Apoptosis-Related Factors in the Luteal Phase of the Domestic Cat and Their Involvement in the Persistence of Corpora Lutea in Lynx.. PLoS One 2015;10(11):e0143414.
                  doi: 10.1371/journal.pone.0143414pubmed: 26599641google scholar: lookup
                4. Galvão A, Tramontano A, Rebordão MR, Amaral A, Bravo PP, Szóstek A, Skarzynski D, Mollo A, Ferreira-Dias G. Opposing roles of leptin and ghrelin in the equine corpus luteum regulation: an in vitro study.. Mediators Inflamm 2014;2014:682193.
                  doi: 10.1155/2014/682193pubmed: 25125800google scholar: lookup
                5. Szóstek AZ, Galvão AM, Hojo T, Okuda K, Skarzynski DJ. Interleukins affect equine endometrial cell function: modulatory action of ovarian steroids.. Mediators Inflamm 2014;2014:208103.
                  doi: 10.1155/2014/208103pubmed: 24719522google scholar: lookup
                6. Kozai K, Hojo T, Tokuyama S, Szóstek AZ, Takahashi M, Sakatani M, Nambo Y, Skarzynski DJ, Okuda K. Expression of aldo-keto reductase 1C23 in the equine corpus luteum in different luteal phases.. J Reprod Dev 2014 Apr 24;60(2):150-4.
                  doi: 10.1262/jrd.2013-120pubmed: 24492656google scholar: lookup
                7. Galvão AM, Ferreira-Dias G, Skarzynski DJ. Cytokines and angiogenesis in the corpus luteum.. Mediators Inflamm 2013;2013:420186.
                  doi: 10.1155/2013/420186pubmed: 23840095google scholar: lookup