The spine apparatus (SA) is a derivate of the smooth endoplasmic reticulum (SER). It is practically always present in dendritic spines possesing a perforated synapse, i.e. the mushroom spine or its sessile variety. A most typical location of the SA is the head of the spine but sometimes it can be found in a neck or -- in the case of the sessile spine -- in the dendritic shaft.
In its most characteristic constellation, one narrow tubule of the SER turns from the dendritic shaft into the neck of the spine to reach the head and branch into two or more stacked flat cisternae (Fig. 1). The larger synapse, the more cisternae. Among them, a dense material is present, called inner dense plates (Figs. 1, 2, 4). A fine filamentous material radiates from these plates to a vesicle-free punctum adherens-like nascent zone of the postsynaptic density (PSD) or occasionally, to the punctum adherens which binds an astrocyte process to the dendritic spine. We call this filamentous band an outer dense plate.
Actin, MAP2, proteinkinase, Ca2+, ATPase, calsequestrin, inositol 1,4,5 - triphospate 3 – kinase and synaptopodin are among substances which were referred in the literature to be present in the SA. We found in the inner dense plates ribosome-like particles, too. An exact significance of the SA is not clear. Its role in buffering (namely sequestring) Ca2+ in the dendritic spine compartment is supposed, but also a synthesis of a proteinaceous material constituting PSD (perhaps even receptors), especially during its extension in a process of the synaptic plasticity (e.g., LTP), is increasingly suggested.
Some authors incorrectly term as SA also profiles of smooth endoplasmic reticulum in spines of cerebellar Purkinje cell dendritic branchlets. Although an occasional parallel configuration of tubules or sacs of endoplasmic reticulum can remind the SA, any signs of higher differentiation and dense plates typical for the SA associated with perforated synapses are lacking in this location. Synapses on Purkinje cell dendritic spines are never of the perforated type.
An organelle identical in appearance with the SA (sometimes called a cisternal organelle in this location) is also found in the axon initial segment (Fig. 5). Its function there is completely unknown. Perhaps a comparative analysis of this organelle together in both these locations will help to uncover its functional significance. Another striking structural similarity exists between the outer dense plates and axial strips described in a subsynaptic cytoplasm of neuromuscular synapses (see Structure of Neuromuscular Junction chapter).
Synaptopodin-deficient mice lack both the SA in dendritic spines and the cisternal organelle in the axon initial segment. It would be very informative to test an eventual relationship of synaptopodin to the thalamic and nuclear lamellar structures.
It is newly supposed that microtubules could contribute to the formation of the dense plates (or vice versa) and also that the SA has some biochemical features of the Golgi apparatus.
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