Filaments, intermediate

Although intermediate filaments are not universally associated with the cytoskeleton, neutrophils possess intermediate filaments of the vimentin type. Vimentin is a rod-shaped molecule of relative molecular mass 57 kDa that readily polymerises under physiological conditions to produce stable filaments 10-12 nm in diameter. Intermediate filaments are more robust than microfilaments and microtubules, and in neutrophils they form an open network of single filaments in the perinuclear space. 

Their role in neutrophil function is not yet established. They may be lo- 

Structure, dynamics, function, and disease of intermediate filaments were reviewed by Fuchs and Weber (1994). 

Type 1 (acidic) 17 polypeptides Type 11 (alkaline) 14 polypeptides Vimentin Desmin 

Intermediate filaments of 7-11 run diameter (Weber and Osborn 1982) of the vimentin type (Franks et al. 1979) are arranged immediately around the cell nucleus, while the remaining cytoplasm reveals only small amounts of 10 mn filaments, which usually do not extend up to the outer membrane of the mononuclear phagocyte (Cain et al. 1982, 1983). With increasing differentiation of monocytes into mature macrophages and epithelioid cell equivalents, a loosening up of the perinuclear vimentin filament network was observed. This development was associated with a straightening of the filaments, which could now be followed into the ectoplasm and into the cytoplasmic processes. 

The application of both crocidolite asbestos (10 pg/ml) and silicon carbide (50 pg/ml) affected the vimentin system of the Syrian hamster epithelial cell line (M3E3/C3) derived from the lung of a foetus on day 15 of gestation in a time-dependent manner (Aufderheide et al. 1994). The vimentin network, which normally appears as a filigree-like pattern throughout the cytoplasm, after exposure to asbestos for 38 h concentrated in bundles. Exposure to silicon carbide induced a concentration of vimentin filaments within the cells at the expense of the normally anastomosing network. 

Human KD fibroblasts on per cell volume basis contained 151.6 ng vimentin/pl (Lai et al. 1993). Protein phosphorylation was augmented by treatment of 600 nM okadaic acid for 1 h in these cells. 

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Mechanical Properties. Although wool has a compHcated hierarchical stmcture (see Fig. 1), the mechanical properties of the fiber are largely understood in terms of a two-phase composite model (27—29). In these models, water-impenetrable crystalline regions (generally associated with the intermediate filaments) oriented parallel to the fiber axis are embedded in a water-sensitive matrix to form a semicrystalline biopolymer. The parallel arrangement of these filaments produces a fiber that is highly anisotropic. Whereas the longitudinal modulus of the fiber decreases by a factor of 3 from dry to wet, the torsional modulus, a measure of the matrix stiffness, decreases by a factor of 10 (30). 

Figure 14.5 The domain organization of intermediate filament protein monomers. Most intermediate filament proteins share a similar rod domain that is usually about 310 amino acids long and forms an extended a helix. The amino-terminal and carboxy-terminal domains are non-a-helical and vary greatly in size and sequence in different intermediate filaments.

The leucine zipper DNA-binding proteins, described in Chapter 10, are examples of globular proteins that use coiled coils to form both homo- and heterodimers. A variety of fibrous proteins also have heptad repeats in their sequences and use coiled coils to form oligomers, mainly dimers and trimers. Among these are myosin, fibrinogen, actin cross-linking proteins such as spectrin and dystrophin as well as the intermediate filament proteins keratin, vimentin, desmin, and neurofilament proteins. 

Figure 14.6 A model of intermediate filament construction. The monomer shown in (a) pairs with an identical monomer to form a coiled-coil dimer (b). The dimers then line up to form an antiparallel tetramer (c). Within each tetramer the dimers are staggered with respect to one another, allowing it to associate with another tetramer (d). In the final 10-nm rope-like intermediate filament, tetramers are packed together in a helical array (e).

North, A.C.T., Steinert, RM., Parry, D.A.D. Coiled-coil stutter and link segments in keratin and other intermediate filament molecules a computer modeling study. Proteins 20 174-184, 1994. 

Cytokeratins are members of the intermediate filament class of cytoskeletal proteins. Cytokeratins are a large protein family comprising two subfamilies of polypeptides, i.e. acidic (type I) and basic (type II) ones. Cytokeratin form tetramers, consisting of two type I and two type II polypeptides arranged in pairs of laterally aligned coiled coils. The distribution of the different type I and II cytokeratins in normal epithelia and in carcinomas is differentiation-related and can be used for cell typing and identification. 

Desmoplakin is the most abundant desmosomal component that plays a critical role in linking intermediate filament networks to the desmosomal plaque. Desmoplakin forms rod-like dimers that bind to intermediate filaments and to the cadherin-associated proteins plakoglobin and plakophilin. Gene knock-out experiments have revealed an essential role of desmoplakin in establishing cell-cell contacts in early mouse embryos. 

Intermediate filaments are present in most animal cells. They are composed of more than 50 proteins which are expressed in a cell-type specific manner. Their diameter is about 10 nm and thus between those of the larger microtubules and the smaller F-actin. They form scaffolds and networks in the cyto- and nucleoplasm. 

Interleukins Intermediate Filaments Intermediate-density Lipoprotein (DDL) Intermittent Claudication Internalization... 

The major types of cytoskeletal filaments are 7-nm-thick microfilaments. 25-nm-thick microtubules, and 10-nm-thick intermediate filaments (IPs). These are respectively composed of actin, tubulin, and a variety of interrelated sparsely soluble fibrous proteins termed intermediate filament proteins. In addition, thick myosin filaments are present in large numbers in skeletal and heart muscle cells and in small numbers in many other types of eukaryotic cells. 

The cytoskeleton also contains different accessory proteins, which, in accordance with their affinities and functions, are designated as microtubule-associated proteins (MAPs), actin-binding proteins (ABPs), intermediate-filament-associated proteins (IFAPs), and myosin-binding proteins. This chapter is focused on those parts of the cytoskeleton that are composed of microfilaments and microtubules and their associated proteins. The subject of intermediate filaments is dealt with in detail in Volume 2. 

Thus far, microtubules and actin filaments and their associated proteins have been discussed to advantage as independent cytoskeletal components. In actual fact, all of the components of the cytoskeleton (including intermediate filaments) are precisely integrated with one another (Langford, 1995), as well as with various cytoplasmic organelles, the nuclear membrane, the plasma membrane, and the extracellular matrix. In its totality the cytoskeleton subserves many coordinated and regulated functions in the cell ... 

The Locomotion of Amoeba The Locomotion of Fibroblastic Cell Types The Locomotion of Leukocytes The Behavior of Locomoting Cells The Role of the Cytoskeleton in Cell Locomotion The Microtubule-Based Cytoskeleton The Intermediate Filament-Based Cytoskeleton The Microfilament-Based Cytoskeleton The Organization of Microfilaments in Cells Microfilament Dynamics and Cell Locomotion Sites of Lamellar Protrusion May Be Determined by the Nucleation of Actin Polymerization... 

Schliwa, M., Honer, B. (1993). Microtubules, centrosomes and intermediate filaments in directed cell movement. Trends Cell Biol. 3, 377-380. 

Vikstrom, K.L., Borisy, G.G., Goldman, R.D. (1989). Dynamic aspects of intermediate filament networks in BHK-21 cells. Proc. Natl. Acad. Sci. USA 86, 549-553. 

Wang, E. (1985). Are cross-bridging strucmres involved in the bundle formation of intermediate filaments and the decrease in locomotion that accompany cell aging J. Cell Biol. 100,1466-1473. 

Inside the typical smooth muscle cell, the cytoplasmic filaments course around the nuclei filling most of the cytoplasm between the nuclei and the plasma membrane. There are two filamentous systems in the smooth muscle cell which run lengthwise through the cell. The first is the more intensively studied actin-myosin sliding filament system. This is the system to which a consensus of investigators attribute most of the active mechanical properties of smooth muscle. It will be discussed in detail below. The second system is the intermediate filament system which to an unknown degree runs in parallel to the actin-myosin system and whose functional role has not yet been completely agreed upon. The intermediate filaments are so named because their diameters are intermediate between those of myosin and actin. These very stable filaments are functionally associated with various protein cytoarchitectural structures, microtubular systems, and desmosomes. Various proteins may participate in the formation of intermediate filaments, e.g., vimentin. 

The analytic validity of an abstract parallel elastic component rests on an assumption. On the basis of its presumed separate physical basis, it is ordinarily taken that the resistance to stretch present at rest is still there during activation. In short, it is in parallel with the filaments which generate active force. This assumption is especially attractive since the actin-myosin system has no demonstrable resistance to stretch in skeletal muscle. However, one should keep in mind, for example, that in smooth muscle cells there is an intracellular filament system which runs in parallel with the actin-myosin system, the intermediate filament system composed of an entirely different set of proteins, (vimentin, desmin, etc.), whose mechanical properties are essentially unknown. Moreover, as already mentioned, different smooth muscles have different extracellular volumes and different kinds of filaments between the cells. 

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. 

Intermediate Filaments Differ From Microfilaments Microtubules... 

An intracellular fibrous system exists of filaments with an axial periodicity of 21 nm and a diameter of 8-10 nm that is intermediate between that of microfilaments (6 nm) and microtubules (23 nm). Four classes of intermediate filaments are found, as indicated in Table 49-13. They are all elongated, fibrous molecules, with a central rod domain, an amino terminal head, and a carboxyl terminal tail. They form a structure like a rope, and the mature filaments are composed of tetramers packed together in a helical manner. They are important structural components of cells, and most are relatively stable components of the cytoskeleton, not undergoing rapid assembly and disassembly and not... 

Table 49-13. Classes of intermediate filaments of eukaryotic cells and their distributions.

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