AMBRA1-regulated autophagy in vertebrate development

• Manuela Antonioli ^[1] ; Federica Albiero ^[1] ; Gian María Fimia ^[1] ; Mauro Piacentini ^[1]
  1. [1] National Institute for Infectious Diseases I.R.C.C.S. "Lazzaro Spallanzani" Rome
• Localización: International journal of developmental biology, ISSN 0214-6282, Vol. 59, Nº. Extra 1-3, 2015 (Ejemplar dedicado a: Cell Death in Development & Tumors), págs. 109-117
• Idioma: inglés
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• Resumen

  • Autophagy is a catabolic process that mediates the lysosomal turn over of organelles and macromolecules, and is strongly activated in stress conditions to ensure cell survival. Autophagy core genes are highly conserved from yeast to mammals, with an increasing number of positive and negative regulators that have evolved in higher eukaryotes. Autophagy takes part in different stages of development, as revealed by alterations in cell proliferation, differentiation and survival during the embryogenesis of organisms carrying mutations in autophagy genes. These defects are ascribed to the ability of autophagy to provide elements for new synthesis or energy production in limiting conditions during embryogenesis, as well as to contribute to the profound cell remodeling that occurs during differentiation. However, many differences have been observed in the phenotypes of autophagy mutant organisms, indicating that these genes have acquired specific functions in particular tissues, which may reflect the ability of autophagy to crosstalk with the main developmental processes. In this review, we discuss the role of upstream regulators of autophagy in the development of different model systems, focusing, in particular, on AMBRA1 (autophagy/beclin-1 regulator-1) and its role in the central nervous system.