Читать книгу Principles of Virology - Jane Flint, S. Jane Flint - Страница 231

A wide range of ligands, fluid, membrane proteins, and lipids are taken into cells from the extracellular milieu by various processes depending on their size (Fig. 5.10). Phagocytosis and endocytosis mediate the uptake of larger and smaller, respectively, molecules and particles. Endocytosis is the mechanism of entry of many viruses (Fig. 5.10 and 5.11). Three pathways of endocytosis have been identified: clathrin-dependent, caveolin-dependent, and clathrin- and caveolin-independent. Clathrin-coated pits can comprise as much as 2% of the surface area of a cell, and some receptors are clustered therein even in the absence of their ligands, whereas others require ligand binding to cluster. Successive transport and fusion with late endosomes exposes the contents of the vesicles to increasingly acidic pH—6.5 to 6.0 (early) and 6.0 to 5.0 (late)—while in lysosomes they are exposed to multiple degradative enzymes. Viral fusion proteins with a high pH threshold for fusion, such as that of vesicular stomatitis virus, mediate entry from early endosomes; but most mediate entry into the cytoplasm from late endosomes, and a few from lysosomes.

The caveolin-dependent pathway participates in transcytosis, signal transduction, and uptake of membrane components and extracellular ligands. Binding of a virus particle to the cell surface activates signal transduction pathways required for pinching off caveolae, which then are transported within the cytoplasm. These vesicles ultimately fuse with the caveosome, a larger membranous organelle that contains caveolin (Fig. 5.11). In contrast to endosomes, the pH of the caveosome lumen is neutral. Some viruses, like echovirus type 1, penetrate the cytoplasm from the caveosome.

Although in cell culture virus particles can enter cells preferentially by one pathway, many viruses appear indiscriminate and enter via multiple pathways. For example, herpes simplex virus can enter cells by three different routes and simian virus 40 is taken up by both caveolin-dependent and clathrin-/caveolin-independent pathways. Influenza A virus can enter cells by both clathrin-dependent endocytosis and macropinocytosis, a process by which extracellular fluid is taken into cells via large vacuoles. Many virus particles are taken up by this pathway, including vaccinia virus, ebolaviruses, and herpesviruses (even though the latter can also fuse at the plasma membrane). Upon receptor binding, viruses that enter cells via macropinocytosis trigger a signaling cascade that leads to changes in cortical actin and ruffling of the plasma membrane (Fig. 5.10). When these plasma membrane extensions retract, the viruses are brought into macropinosomes and eventually leave these vesicles via membrane fusion. A more dramatic rearrangement of actin filaments leads to the formation of filopodia, thin extensions of the plasma membrane. Virus particles of polyomaviruses can be visualized moving laterally on the plasma membrane on filopodia, and filopodia bridges participate in cell-to-cell spread of retrovirus particles in cells in culture (Chapter 13).

Figure 5.11 Virus entry and movement in the cytoplasm. Examples of various routes of virus entry are shown. Fusion at the plasma membrane releases the nucleocapsid or subviral components (lower left side of the cell) that can travel on actin filaments and microtubules. Uptake of virus particles by endocytosis can be either clathrin dependent, caveolin dependent, or clathrin and caveolin independent. Clathrin-dependent endocytosis (top left side of the cell) commences with binding to a specific cell surface receptor followed by diffusion into an invagination of the plasma membrane coated with the protein clathrin on the cytosolic side (clathrin-coated pits). The coated pit further invaginates and pinches off, a process that is facilitated by the GTPase dynamin. Within a few seconds, the clathrin coat is lost and the vesicles fuse with small, smooth-walled vesicles located near the cell surface, called early endosomes. The lumen of early endosomes is mildly acidic (pH 6.5 to 6.0), a result of energy-dependent transport of protons into the interior of the vesicles by a membrane proton pump. The contents of the early endosome are then transported via endosomal carrier vesicles to late endosomes located closer to the nucleus. The lumen of late endosomes is more acidic (pH 6.0 to 5.0). Late endosomes in turn fuse with lysosomes, which are vesicles containing a variety of enzymes that degrade sugars, proteins, nucleic acids, and lipids. Particle uncoating usually occurs from early or late endosomes. Virus particles may enter cells by a dynamin- and caveolin-dependent endocytic pathway (right side of the cell). Caveolae are distinguished from clathrin-coated vesicles by their flask-like shape, their smaller size, the absence of a clathrin coat, and the presence of a marker protein called caveolin. Three types of caveolar endocytosis have been identified. Dynamin 2-dependent endocytosis by caveolin 1-containing caveolae is observed in cells infected with simian virus 40 and polyomavirus. Dynamin 2-dependent, noncaveolar, lipid raft-mediated endocytosis occurs during echovirus and rotavirus infection, while dynamin-independent, noncaveolar, raft-mediated endocytosis is also observed during simian virus 40 and polyomavirus infection. This pathway brings virions to the endoplasmic reticulum via the caveosome, a pH-neutral compartment. Clathrin- and caveolin-independent endocytic pathways of viral entry have also been described (top center-right of cell). Movement of endocytic vesicles within cells occurs on actin filaments or microtubules, the components of the cytoskeleton. Actin filaments are two-stranded helical polymers of actin. They are dispersed throughout the cell but are most highly concentrated beneath the plasma membrane, where they are connected via integrins and other proteins to the extra-cellular matrix. Transport along actin filaments is accomplished by myosin motors. Microtubules are 25-nm hollow cylinders made of tubulin. They radiate from the centrosome to the cell periphery. Movement on microtubules is mediated by kinesin and dynein motors.