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the particles, but they also organize these particles and the content of particles, as
seems to be the case with the transport of neurotransmitter vesicles along axons in
the synapse ( Glade et al., 2004 ). They determine the arrangement and movement
of organelles (including the movement and separation of chromosomes during
mitosis/meiosis) in the cell; they transport nuclei to the surface of the embryo during
the blastoderm stage, thus determining the position of the nucleus within the cell.
Actin (Micro-) Filaments
These polymers of actin molecules are the thinnest (7 nm) ( Figure 1.19 ) of all
three types of cytoskeleton filaments. Actin polymerization generates a push force,
whereas binding with myosin causes the actin cytoskeleton to contract. Actin fila-
ments respond to the binding of a number of proteins with changes in the organi-
zation of the actin cytoskeleton. The actin cytoskeleton responds to a number of
external signals (hormones, growth factors, etc.), and the mediators of these external
influences are approximately 20 Rho guanosine triphosphatase (GTPase) enzymes
( Sit and Manser, 2011 ).
Intermediate Filaments
As their name indicates, these filaments are intermediate in average diameter (12 nm)
between microtubules and actin filaments ( Figure 1.20 ). They are a family of fibrous
proteins encoded by about 70 genes. They exist in monomer and dimmer forms and
contribute to maintaining cell shape but do not participate in cell motility ( Lodish
et al., 2000 ).
Figure 1.20 Structural organization of microtubule, microfilament, and intermediate
filament (from http://www.tutorvista.com/content/biology/biology-iii/cell-organization/
nonmembranous-cell-organelles.php ) .
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