Selective autophagy, lipophagy and mitophagy, in the Harderian gland along the oestrous cycle: a potential retrieval effect of melatonin

[EN]Sexual dimorphism has been reported in many processes. However, sexual bias in favour of the use of males is very present in science. One of the main reasons is that the impact of hormones in diverse pathways and processes such as autophagy have not been properly addressed in vivo. The Harderian...

Descripción completa

Detalles Bibliográficos
Autores: García Macia, Marina, Santos Ledo, Adrián, Caballero, Beatriz, Rubio-González, Adrian, de Luxán-Delgado, Beatriz, Potes, Yaiza, Rodríguez-González, Susana Mª., Boga, José Antonio, Coto-Montes, Ana
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2019
País:España
Institución:Universidad de Salamanca (USAL)
Repositorio:GREDOS. Repositorio Institucional de la Universidad de Salamanca
OAI Identifier:oai:gredos.usal.es:10366/161912
Acceso en línea:http://hdl.handle.net/10366/161912
Access Level:acceso abierto
Palabra clave:Melatonin
Autophagy
Mouse
Lipophagy
Sexual cycle
Mitophagy
Harderian Gland
Sexual Behavior, Animal
Reproduction
Rodentia
2407 Biología Celular
2401 Biología Animal (Zoología)
2411.16 Fisiología de la Reproducción
glándula de Harder
reproducción
autofagia
conducta sexual animal
melatonina
Descripción
Sumario:[EN]Sexual dimorphism has been reported in many processes. However, sexual bias in favour of the use of males is very present in science. One of the main reasons is that the impact of hormones in diverse pathways and processes such as autophagy have not been properly addressed in vivo. The Harderian gland is a perfect model to study autophagic modulation as it exhibits important changes during the oestrous cycle. The aim of this study is to identify the main processes behind Harderian gland differences under oestrous cycle and their modulator. In the present study we show that redox-sensitive transcription factors have an essential role: NF-κB may activate SQSTM1/p62 in oestrus, promoting selective types of autophagy: mitophagy and lipophagy. Nrf2 activation in dioestrus, leads the retrieval phase and restoration of mitochondrial homeostasis. Melatonin’s receptors show higher expression in dioestrus, leading to decreases in pro-inflammatory mediators and enhanced Nrf2 expression. Consequently, autophagy is blocked, and porphyrin release is reduced. All these results point to melatonin as one of the main modulators of the changes in autophagy during the oestrous cycle.