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Dendritic spines
Dendritic
Spines
Rafael Yuste
MIT Press (2010)
This review refers mainly
to
chapter 4 of this book, which deals with the internal make up of the
dendritic spines, an aspect which bears on controversies relating to
Hameroff's
attempt to describe an implementation of quantum consciousness.
Dendritic
spines are recipients of synaptic inputs, and almost every spine has an
excitatory input, while some have both excitatory and inhibitory inputs.
Spiny
dendrites appear to have developed to integrate inputs from as many
sources as
possible. Connectivity is combined with plasticity for the individual
spines,
which is seen as increasing flexibility and computing power. The spines
project
from the shaft or main body of the dendrites, with a narrow neck where
they
join to the main shaft and a broader head. Spines are thought to be
capable of some
of their own protein synthesis.
Spines
are structurally flexible with a cytoskeleton based on actin rather than
microtubules. Actin and Rho pathways in the spines are well placed to
control
their shape and function. The spines are important for inputs of
glutamate and
they possess all four types of glutamate receptor. The heads of spines
are
filled with a network of actin filaments that interact with the post
synaptic
density (PSD). In the spine neck, actin filaments are formed into long
bundles.
Only 5% of the spine's actin is stable. The spines also contain a number
of
actin related proteins, and it is thought that these may be involved in
functions such as vesicle and protein transport, spine shape, anchoring
of
membrane proteins, notably glutamate receptors. Many actin binding
proteins can
be regulated by Ca2+ calcium ions, and this may be important in
regulating
actin activity in the spines. The actin binding proteins may also
influence the
formation and shape of spines. The abscence of a tubulin suggests that
the
spines need to have limited stability. Spines have to move so as to more
efficiently connect with axons. It is suggested here that changes in the
shape
of spines are involved in synaptic plasticity.
Dendritic
spines also contain cell-adhesion molecules, linked to the actin
cytoskeleton.
Cadherin molecules interact with actin filaments, and may be involved in
synaptic plasticity. These molecules appear to be localised in the
adhesive
structure around the post synaptic density. The spine membranes also
contain
both sodium and potassium ion channels. P. In summary, dendritic spines
can be
viewed as nanomachines involving membrane receptors and channels, cell
adhesion
proteins, cytoskeleton components and a variety of other molecules. It
appears
that the biochemistry of each spine is independently regulated to
specifically
regulate the input of each synapse. The spine represents an
exceptionally
complex environment with a very precise regulation of numbers of
molecules and
their positioning. Every molecular pathway is linked to the actin
cytoskeleton.
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