Abstract
Presynaptic terminals occur along unmyelinated axons in specialized compartments called axonal varicosities or synaptic boutons. Since the first descriptions of varicose axons by Cajal and others, the spatial organization of varicosities along axons has attracted the attention of neuroscientists. Quantitative light- and electron-microscopic analyses of varicosity spacing in the cerebellum and elsewhere have recently provided a clearer picture of this organization, and theoretical analyses now incorporate varicosity spacing as an essential parameter in structural models of neural connectivity. Here we review the salient features of varicosity spacing, with emphasis on cerebellar parallel fibers as a model system. Measured globally across the entire≈ 5 mm lengths of parallel fibers, the overall mean spacing of varicosities is 5.2 μm. Measured locally, however, mean spacing follows a proximodistal gradient, increasing with distance from the point of bifurcation from the ascending axon. Measured at the level of individual varicosities, parallel fiber varicosity distributions follow a distinct pattern characterized by a fixed relationship between the spacing variability and mean. This pattern equally describes varicosity distributions in a number of other brain regions, and therefore appears to constitute a general scaling relationship for excitatory varicose axons. We further discuss evidence for common principles underlying the placement of both varicosities and synapses along axons.
This is a preview of subscription content, access via your institution.
References
Palay SL, Chan-Palay V. Cerebellar cortex: cytology and organization. New York: Springer, 1974: 63–99.
Pichitpornchai C, Rawson JA, Rees S. Morphology of parallel fibers in the cerebellar cortex of the rat: an experimental light and electron microscopic study with biocytin. J Comp Neurol 1994; 342: 206–220.
Llinás R. General discussion: radial connectivity in the cerebellar cortex. A novel view regarding the functional organization of the molecular layer. In: Palay SL, Chan-Palay V, editors. The Cerebellum: new vistas. 1982.
Bower JM, Woolston DC. Congruence of spatial organization of tactile projections to granule cell and Purkinje cell layers of cerebellar hemispheres of the albino rat: vertical organization of cerebellar cortex. J Neurophysiol 1983; 49: 745–766.
Isope P, Barbour B. Properties of unitary granule cell → Purkinje cell synapses in adult rat cerebellar slices. J Neurosci 2002; 22: 9668–9678.
Hellwig B, Schüz A, Aertsen A. Synapses on axon collaterals of pyramidal cells are spaced at random intervals: a Golgi study in the mouse cerebral cortex. Biol Cybern 1994; 71: 1–12.
Kincaid AE, Zhengh T, Wilson CJ. Connectivity and convergence of single corticostriatal axons. J Neurosci 1998; 18: 4722–4731.
Lu SM, Lin RC. Thalamic afferents of the rat barrel cortex: a light- and electron-microscopic study using Phaseolus vulgaris leucoagglutinin as an anterograde tracer. Somatosens Mot Res 1993; 10: 1–16.
Amir Y, Harel M, Malach R. Cortical hierarchy reflected in the organization of intrinsic connections in macaque monkey visual cortex. J Comp Neurol 1993; 334: 19–46.
Martin KAC, Whitteridge D. Form, function and intracortical projections of spiny neurones in the striate visual cortex of the cat. J Physiol 1984; 353: 463–504.
Sasaki-Sherrington SE, Jacobs JR, Stevens JK. Intracellular control of axial shape in non-uniform neurites: a serial electron microscopic analysis of organelles and microtubules in AI and AII retinal amacrine neurites. J Cell Biol 1984; 98: 1279–1290.
Shepherd GMG, Raastad M, Andersen P. General and variable features of varicosity spacing along unmyelinated axons in the hippocampus and cerebellum. Proc Natl Acad Sci USA 2002; 99: 6340–6345.
Sholl DA. The Organization of the Cerebral Cortex. London: Wiley, 1956.
Braitenberg V, Schüz A. Cortex: statistics and geometry of neuronal connectivity; 2nd edn. Berlin: Springer-Verlag, 1998.
White EL. Cortical circuits: synaptic organization of the cerebral cortex structure, function and theory. Boston: Birkhauser, 1998.
Xu-Friedman MA, Harris KM, Regehr WG. Three-dimensional comparison of ultrastructural characteristics at depressing and facilitating synapses onto cerebellar Purkinje cells. J Neurosci 2001; 21: 6666–6672.
Shepherd GMG, Harris KM. Three-dimensional structure and composition of CA3→ CA1 axons in rat hippocampal slices: implications for presynaptic connectivity and compartmentalization. J Neurosci 1998; 18: 8300–8310.
Harvey RJ, Napper RMA. Quantitative study of granule and Purkinje cells in the cerebellar cortex of the rat. J Comp Neurol 1988; 274: 151–157.
Napper RMA, Harvey RJ. Number of parallel fiber synapses on an individual Purkinje cell in the cerebellum of the rat. J Comp Neurol 1988; 274: 168–177.
Chklovskii DB, Schikorski T, Stevens CF. Wiring optimization in cortical circuits. Neuron 2002; 34: 341–347.
Stepanyants A, Hof PR, Chklovskii DB. Geometry and structural plasticity of synaptic connectivity. Neuron 2002; 34: 275–288.
Carter AG, Regehr WG. Prolonged synaptic currents and glutamate spillover at the parallel fiber to stellate cell synapse. J Neurosci 2000; 20: 4423–4434.
Arnth-Jensen N, Jabaudon D, Scanziani M. Cooperation between independent hippocampal synapses is controlled by glutamate uptake. Nat Neurosci 2002; 5: 325–331.
Hartell NA. Parallel fiber plasticity. Cerebellum 2002; 1: 3–18.
Wang Y, Gupta A, Toledo-Rodriguez M, Wu CZ, Markram H. Anatomical, physiological, molecular and circuit properties of nest basket cells in the developing somatosensory cortex. Cereb Cortex 2002; 12: 395–410.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Shepherd, G.M.G., Raastad, M. Axonal varicosity distributions along parallel fibers: a new angle on a cerebellar circuit. Cerebellum 2, 110–113 (2003). https://doi.org/10.1080/14734220310011407
Received:
Revised:
Accepted:
Issue Date:
DOI: https://doi.org/10.1080/14734220310011407