Сopper nanoparticles supported on charcoal and betacellulin – Two novel stimulators of ovarian granulosa cell functions and their functional interrelationships

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Título: Сopper nanoparticles supported on charcoal and betacellulin – Two novel stimulators of ovarian granulosa cell functions and their functional interrelationships
Autor/es: Sirotkin, Alexander V. | Loncová, Barbora | Fabova, Zuzana | Bartušová, Michaela | Martín-García, Iris | Harrath, Abdel Halim | Alonso, Francisco
Grupo/s de investigación o GITE: Nuevos Materiales y Catalizadores (MATCAT)
Centro, Departamento o Servicio: Universidad de Alicante. Departamento de Química Orgánica | Universidad de Alicante. Departamento de Química Inorgánica | Universidad de Alicante. Instituto Universitario de Síntesis Orgánica
Palabras clave: Copper | Nanoparticles | Ovary | Proliferation | Apoptosis
Fecha de publicación: 1-feb-2024
Editor: Elsevier
Cita bibliográfica: Theriogenology. 2024, 218: 137-141. https://doi.org/10.1016/j.theriogenology.2024.01.028
Resumen: The present experiments are aimed to examine the effect of copper nanoparticles supported on charcoal (CuNPs/ C), growth factor betacellulin (BTC) and their interrelationships in the control of ovarian cell functions. Porcine ovarian granulosa cells were cultured in the presence of CuNPs/C (0, 1, 10 or 100 ng/ml), BTC (100 ng/ml) and the combination of both, CuNPs/C + BTC. Markers of cell proliferation (BrDU incorporation), of the S-phase (PCNA) and G-phase cyclin B1) of the cell cycle, markers of extrinsic (nuclear DNA fragmentation) and cytoplasmic/mitochondrial apoptosis (bax and caspase 3), and the release of progesterone and estradiol were assessed by BrDU test, TUNEL, quantitative immunocytochemistry and ELISA. Both CuNPs/C and BTC, when added alone, increased the expression of all the markers of cell proliferation, reduced the expression of all apoptosis markers and stimulated progesterone and estradiol release. Moreover, BTC was able to promote the CuNPs/C action on the accumulation of PCNA, cyclin B1, bax and estradiol output. These observations demonstrate the stimulatory action of both CuNPs/C and BTC on ovarian cell functions, as well as the ability of BTC to promote the action of CuNPs/C on ovarian cell functions.
Patrocinador/es: This research was financially supported by the Scientific Grant Agency of the Ministry of Education, Science, and Sport of the Slovak Republic (VEGA) (project no. VEGA 1/0680/22), by the King Saud University, Riyadh, Saudi Arabia (Researchers Supporting Project no. RSP2023R17) and by the Generalitat Valenciana, Spain (GV; grant no. CIAICO/2022/017).
URI: http://hdl.handle.net/10045/140751
ISSN: 0093-691X (Print) | 1879-3231 (Online)
DOI: 10.1016/j.theriogenology.2024.01.028
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: © 2024 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
Revisión científica: si
Versión del editor: https://doi.org/10.1016/j.theriogenology.2024.01.028
Aparece en las colecciones:INV - MATCAT - Artículos de Revistas

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