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In biology, a phagolysosome, or endolysosome, is a cytoplasmic body formed by the fusion of a phagosome with a lysosome in a process that occurs during phagocytosis. Formation of phagolysosomes is essential for the intracellular destruction of microorganisms and pathogens .
Phagocytosis of a bacterium, showing the formation of phagosome and phagolysosome In cell biology , a phagosome is a vesicle formed around a particle engulfed by a phagocyte via phagocytosis . Professional phagocytes include macrophages , neutrophils , and dendritic cells (DCs).
The phagosome is the organelle formed by phagocytosis of material. It then moves toward the centrosome of the phagocyte and is fused with lysosomes, forming a phagolysosome and leading to degradation. Progressively, the phagolysosome is acidified, activating degradative enzymes. [10] [15] Degradation can be oxygen-dependent or oxygen-independent.
They take various forms (with various names) throughout the body (e.g., histiocytes, Kupffer cells, alveolar macrophages, microglia, and others), but all are part of the mononuclear phagocyte system. Besides phagocytosis, they play a critical role in nonspecific defense ( innate immunity ) and also help initiate specific defense mechanisms ...
For example, following phagocytosis, the ingested particle (or phagosome) fuses with a lysosome containing hydrolytic enzymes to form a phagolysosome; the pathogens or food particles within the phagosome are then digested by the lysosome's enzymes.
The spleen is the second largest unit of the mononuclear phagocyte system. The monocyte is formed in the bone marrow and transported by the blood; it migrates into the tissues, where it transforms into a histiocyte or a macrophage.
Extracellular proteins are endocytosed into a phagosome, which subsequently fuses with a lysosome to create a phagolysosome. Within the phagolysosome, lysosomal enzymes degrade the proteins into peptide fragments. These fragments are then loaded into the peptide-binding groove of the MHC class II molecule.
In neurons, autophagosomes are generated at the neurite tip and mature (acidify) as they travel towards the cell body along the axon. [9] This axonal transport is disrupted if huntingtin or its interacting partner HAP1 , which colocalize with autophagosomes in neurons, are depleted.