Cytoskeleton cellular

Fulton, A. B. (1984) The Cytoskeleton Cellular Architecture and Choreography, Chapman and Hall, New York... 

Tiwari, S.C., Wick, S.M., Williamson, R.E., Gunning, B.E. (1984). Cytoskeleton and integration of cellular function in cells of higher plants. J. Cell Biol. 99,63S-69S. 

Nonmuscle cells perform mechanical work, including self-propulsion, morphogenesis, cleavage, endocytosis, exocytosis, intracellular transport, and changing cell shape. These cellular functions are carried out by an extensive intracellular network of filamentous structures constimting the cytoskeleton. The cell cytoplasm is not a sac of fluid, as once thought. Essentially all eukaryotic cells contain three types of filamentous struc-mres actin filaments (7-9.5 nm in diameter also known as microfilaments), microtubules (25 nm), and intermediate filaments (10-12 nm). Each type of filament can be distinguished biochemically and by the electron microscope. 

The cellular cytoskeleton, primarily composed of microfilaments, microtubules, and intermediate filaments, provides structural support and enables cell motility. The cytoskeleton is composed of biological polymers and is not static. Rather, it is capable of dynamic reassembly in less than a minute [136], The cytoskeleton is built from three key components, the actin filaments, the intermediate filaments, and the microtubules. The filaments are primarily responsible for maintaining cell shape, whereas the microtubules can be seen as the load-bearing elements that prevent a cell from collapsing [136], The cytoskeleton protects cellular structures and connects mechanotransductive pathways. Along with mechanical support, the cytoskeleton plays a critical role in many biological processes. 

To diffuse rapidly in the plane of the membrane (lateral diffusion), a molecule must simply move around in the lipid environment (including the polar head groups). It need not change how it interacts with phospholipids or with water since it is constantly exposed to pretty much the same environment. Lateral diffusion can be slowed (or prevented) by interactions between membrane proteins and the cellular cytoskeleton. This spatially restricts a plasma membrane protein to a localized environment. 

Proteins of the cytoskeleton play a central role in the creation and maintenance of cell shapes in all tissues. They serve multiple roles in eukaryotic cells. First, they provide structural organization for the cell interior, helping to establish metabolic compartments. Second, cytoskeletal structures serve as tracks for intracellular transport, which creates and maintains differentiated cellular functions. Finally, the cytoskeleton comprises the core framework of cellular morphologies. 

The integrins comprise a family of cell-surface proteins that are involved in adhesion, a process vital for many processes, such as anchorage, migration, growth and differentiation. Cells may adhere to other cells (cell-cell adhesion) or may interact with soluble molecules that constitute the extracellular matrix (cell-extracellular matrix). The integrins are linked to elements of the cytoskeleton, and so they provide a bridge between the external cellular environment and intracellular activation processes. 

The family of eukaryotic Ras-like small GTPases may be divided into subfamilies, namely those of ARF, Rab, Ran, Ras, Rho, and Sar (ARF, RAB, RHO, RAS, RHO, SAR), which all contain representatives from fungi, plants, and metazoa. Consequently, these subfamilies and their cellular functions are likely to have emerged early in eukaryotic history. This implies that the last common ancestor of fungi, plants, and metazoa possessed vesicular transport (ARF and Sar), membrane trafficking (Rab), nuclear transport (Ran), signal transduction (Ras), and regulation of the actin cytoskeleton (Rho) functions. 

Isfort, R.J., Cody, D.B., Doerson, C., Kerckaert, G.A., and LeBoeuf, R.A., Alterations in cellular differentiation, mitogenesis, cytoskeleton and growth characteristics during Syrian hamster embryo cell multistep in vitro transformation, Int. J. Cancer, 59, 114, 1994. 

Synthetic lipids and peptides have been found to self-assemble into tubules [51,52]. Several groups have used these tubules as templates [17,51,53-56]. Much of this work has been the electroless deposition of metals [51,54]. Electrolessly plated Ni tubules were found to be effective field emission cathode sources [55]. Other materials templated in or on self-assembled lipid tubules include conducting polymer [56] and inorganic oxides [53]. Nanotubules from cellular cytoskeletons have also been used for electroless deposition of metals [57]. 

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