Cytoskeleton

The cytoskeleton is a structural "scaffold" or "skeleton" that is present inside all eukaryotic cells. This dynamic, three dimensional structure fills the cytoplasms of cells; it maintains their shape, and enables them to move, using structures such as flagella and cilia. It also has important roles in the intracellular transport of vesicles and organelles) and in cell division.

Eukaryotic cells

Actin cytoskeleton of mouse embryo fibroblasts, stained with phalloidin

Eukaryotic cells contain three kinds of cytoskeletal filaments:

Microfilaments, which are about 7 nm in diameter, are composed of two actin chains oriented in an helicoidal shape. Actin is a contractile protein, and is the most abundant protein in cells. In muscles cells, the association of microfilaments with another protein, myosin, is responsible for muscle contraction. Microfilaments can also carry out cellular movements including gliding, contraction, and cytokinesis. They are mostly concentrated just beneath the plasma membrane, as they keep cellular shape, form cytoplasmatic protuberances (like pseudopodia and microvilli), and participate in some cell-to-cell or cell-to-matrix junctions and in the transduction of signals. They are also important for cytokinesis and, along with myosin, muscular contraction.

Intermediate filaments, 8-11 nanometers in diameter, are the more stable (strongly bound) and heterogeneous constituents of the cytoskeleton; they provide the tensile strength of a cell, and determine its internal structure; for example, they are structural components of the nuclear envelope and of the sarcomeres. They also participate in some cell-cell and cell-matrix junctions. Many intermediate filaments are made of vimentins. Others, in cells of the skin hair and nails, are made of keratin. Some filaments, made of laminin, give structural support to the nuclear envelope.

Microtubules are hollow cylinders of about 25 nm in diameter, formed by 13 protofilaments which are polymers of alpha and beta tubulin. Microtubules act as a scaffold to determine cell shape, and they provide "tracks" which cell organelles and vesicles move along. Microtubules also form the spindle fibers for separating chromosomes during mitosis. When arranged in geometric patterns inside flagella and cilia, they are used for locomotion. They have a very dynamic behaviour, binding GTP for polymerization. They are organized by the centrosome.

In, for example, the epithelial (skin) cells of the intestine, microfilaments that project into the villi, give shape to the cell surface; microtubules project from the centrosome to the cell periphery; and intermediate filaments connect adjacent cells through desmosomes.

Prokaryote cells

The cytoskeleton was thought to be a feature only of eukaryotic cells, but homologues of the major proteins of the eukaryotic cytoskeleton have been found in prokaryotes..

FtsZ was the first of these to be identified. Like tubulin, FtsZ forms filaments in the presence of GTP, but these filaments do not group into tubules. During cell division, FtsZ is the first protein to move to the division site, and is essential for recruiting other proteins that produce a new cell wall between the dividing cells.

Prokaryotic actin-like proteins, such as MreB, are involved in maintaining cell shape. All non-spherical bacteria have genes that encode actin-like proteins; these proteins form a helical network beneath the cell membrane that guides the proteins involved in cell wall biosynthesis.

Some plasmids encode a partitioning system that involves an actin-like protein ParM. Filaments of ParM exhibit dynamic instability, and may partition plasmid DNA into the dividing daughter cells by a mechanism like that used by microtubules during eukaryotic mitosis.

The bacterium Caulobacter crescentus expresses a protein, crescentin, that is related to the intermediate filaments of eukaryotic cells. Crescentin is also involved in maintaining cell shape, but how it does this is unclear.