Phagocytosis is a cellular process where the plasma membrane surrounds and engulfs particles. Once the particle is enclosed within a vesicle, the protein clathrin detaches, and the vesicle merges with a lysosome to degrade the material, forming an endosome. Nutrients from this degradation are then released into the extracellular fluid when the endosome fuses back with the plasma membrane.
Pinocytosis, known as "cell drinking," involves the uptake of extracellular fluid and dissolved molecules, resulting in smaller vesicles compared to phagocytosis. A form of pinocytosis, called potocytosis, uses the protein caveolin and is characterized by smaller vesicles that transport molecules through the cell for release on the opposite side (transcytosis).
This targeted form of endocytosis relies on receptor proteins that bind specific substances. Clathrin again plays a role by binding to the cytoplasmic side of the membrane to form vesicles. Effective receptor-mediated endocytosis is crucial for removing substances like low-density lipoproteins (LDL) from the bloodstream. Defective receptors can lead to diseases such as familial hypercholesterolemia, resulting in high cholesterol levels.
In exocytosis, waste or other materials are expelled from the cell. Vesicles containing these materials fuse with the plasma membrane, releasing their contents into the extracellular space. This process is involved in the secretion of neurotransmitters and extracellular matrix proteins.
Bulk transport methods, including phagocytosis and pinocytosis, are energy-dependent processes used to move large entities in and out of the cell. Phagocytosis allows for the engulfing of large particles, while pinocytosis takes in smaller volumes of fluid. The reverse process of expelling materials from a cell is termed exocytosis.
In biological systems, substances can be transported through various methods which vary in energy requirements: