Dissection of the autophagic route in oocytes from atretic follicles


Por: Castro-Cruz, Abraham, Echeverria, Olga M. M., Sanchez-Sanchez, Luis, Munoz-Velasco, Israel, Juarez-Chavero, Silvia, Torres-Ramirez, Nayeli, Vazquez-Nin, Gerardo H. H., Escobar, Maria Luisa

Publicada: 1 mar 2023 Ahead of Print: 1 ene 2023
Resumen:
Background InformationAutophagy is a conserved process that functions as a cytoprotective mechanism; it may function as a cell death process called programmed cell death type II. There is considerable evidence for the presence of autophagic cell death during oocyte elimination in prepubertal rats. However, the mechanisms involved in this process have not been deciphered. ResultsOur observations revealed autophagic cell death in oocytes with increased labeling of the autophagic proteins Beclin 1, light chain 3 A (LC3 A), and lysosomal-associated membrane protein 1 (Lamp1). Furthermore, mTOR and phosphorylated (p)-mTOR (S2448) proteins were significantly decreased in oocytes with increased levels of autophagic proteins, indicating autophagic activation. Moreover, phosphorylated protein kinase B (p-AKT) was not expressed by oocytes, but mitogen-activated protein kinase/extracellular signalregulated kinase (MAPK/ERK) signaling was observed. Additionally, selective and elevated mitochondrial degradation was identified in altered oocytes. ConclusionsAll these results suggest that mTOR downregulation, which promotes autophagy, could be mediated by low energy levels and sustained starvation involving the phosphoinositide 3-kinase (PI3K)/AKT/mTOR and MAPK/ERK pathways. SignificanceIn this work, we analyzed the manner in which autophagy is carried out in oocytes undergoing autophagic cell death by studying the behavior of proteins involved in different steps of the autophagic pathway.

Filiaciones:
Castro-Cruz, Abraham:
 Univ Nacl Autonomade Mexico, Col Univ Nacl Autonoma Mex, Dept Biol Celular, Lab Microscopia Elect,Fac Ciencias, Ciudad de Mexico, Mexico

Echeverria, Olga M. M.:
 Univ Nacl Autonomade Mexico, Col Univ Nacl Autonoma Mex, Dept Biol Celular, Lab Microscopia Elect,Fac Ciencias, Ciudad de Mexico, Mexico

Sanchez-Sanchez, Luis:
 Univ Nacl Autonoma Mexico, Fac Estudios Super Zaragoza, Lab Biol Mol Canc, Lab 6,2 do piso, Mexico City, Mexico

Munoz-Velasco, Israel:
 Univ Nacl Autonomade Mexico, Col Univ Nacl Autonoma Mex, Dept Biol Celular, Lab Microscopia Elect,Fac Ciencias, Ciudad de Mexico, Mexico

Juarez-Chavero, Silvia:
 Univ Nacl Autonomade Mexico, Col Univ Nacl Autonoma Mex, Dept Biol Celular, Lab Microscopia Elect,Fac Ciencias, Ciudad de Mexico, Mexico

Torres-Ramirez, Nayeli:
 Univ Nacl Autonomade Mexico, Col Univ Nacl Autonoma Mex, Dept Biol Celular, Lab Microscopia Elect,Fac Ciencias, Ciudad de Mexico, Mexico

Vazquez-Nin, Gerardo H. H.:
 Univ Nacl Autonomade Mexico, Col Univ Nacl Autonoma Mex, Dept Biol Celular, Lab Microscopia Elect,Fac Ciencias, Ciudad de Mexico, Mexico

Escobar, Maria Luisa:
 Univ Nacl Autonomade Mexico, Col Univ Nacl Autonoma Mex, Dept Biol Celular, Lab Microscopia Elect,Fac Ciencias, Ciudad de Mexico, Mexico

 Univ Nacl Autonoma Mexico, Col Univ Nacl Autonoma Mexico, Fac Ciencias, Dept Biol Celular, Ave Univ 3000, Ciudad de Mexico 04510, Mexico
ISSN: 02484900





BIOLOGY OF THE CELL
Editorial
Wiley-Blackwell, 111 RIVER ST, HOBOKEN 07030-5774, NJ USA, Reino Unido
Tipo de documento: Article
Volumen: 115 Número: 3
Páginas:
WOS Id: 000919128500001
ID de PubMed: 36571578
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