Autophagolysosome
Autophagolysosome is a cellular structure that forms during the process of autophagy. Autophagy is a cellular degradation pathway that involves the delivery of cytoplasmic cargo to the lysosome. Autophagolysosomes are the final product of this process, where the cargo is degraded.
Formation[edit | edit source]
The formation of an autophagolysosome involves several steps. First, a portion of the cytoplasm, or a specific organelle, is enclosed by a double-membrane structure known as an autophagosome. The autophagosome then fuses with a lysosome to form an autophagolysosome. The contents of the autophagolysosome are then degraded by lysosomal enzymes.
Function[edit | edit source]
The primary function of autophagolysosomes is to degrade and recycle cellular components. This process is essential for maintaining cellular homeostasis and responding to changes in nutrient availability. Autophagolysosomes also play a role in the removal of damaged organelles and proteins, and in the defense against intracellular pathogens.
Role in disease[edit | edit source]
Defects in autophagolysosome formation or function can lead to a variety of diseases, including neurodegenerative diseases, cancer, and infections. For example, mutations in genes involved in autophagosome formation can lead to neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease. In cancer, autophagy can have both tumor-suppressive and tumor-promoting roles, depending on the context.
See also[edit | edit source]
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Contributors: Prab R. Tumpati, MD