ABSTRACT
The source of the autophagosome membrane, and the formation of the autophagosome remain the most important questions for understanding autophagy. Fundamentally, the process of autophagosome formation is similar between yeast and mammalian cells and many of the proteins involved (called the autophagy-related (Atg) proteins) are known, having been first discovered in yeast. However, both in yeast and mammalian cells, the molecular details are missing to explain how the double-membrane autophagosome is formed. Important advances in our understanding of the formation process have recently been obtained, and here, we review and interpret these data in the context of well-known paradigms of membrane trafficking to develop some hypothetical models for how an autophagosome forms in mammalian cells.
Subject(s)
Autophagy/physiology , Phagosomes/physiology , Transport Vesicles/physiology , Animals , Humans , Microtubule-Associated Proteins/metabolism , Protein Kinases/metabolism , SNARE Proteins/metabolism , Signal Transduction/physiology , Ubiquitin/metabolism , rab GTP-Binding Proteins/metabolismABSTRACT
During the 1975-1984 period, 93 infants weighing 1500 g or less were transferred to the Magenta Perinatal Center Hospital. The survival rate at discharge was 82.9% for infants transferred in utero and 63.5% for infants transferred postnatally (p less than 0.05). The incidence of major neurological sequelae was 3.1% and 23.3% respectively (p less than 0.02). This experience confirms that the high risk pregnancies should be referred to the Perinatal Center for optimal care of the mother, fetus and newborn infant.
