Wheat germ agglutinin binding sites in the adult mouse cerebellum: Light and electron microscopic studies
- 8 July 1986
- journal article
- research article
- Published by Wiley in Journal of Comparative Neurology
- Vol. 249 (2) , 170-185
- https://doi.org/10.1002/cne.902490205
Abstract
The binding properties of derivatized wheat germ agglutinin (WGA) have been examined in fixed tissue sections from the adult mouse cerebellum and also in axonal tracing paradigms following cerebellar injections. The aim of these studies is to begin to distinguish the roles different binding sites may play in generating diverse biological activities which lead to neuronal uptake and axonal transport of lectins or glycoconjugates. Vibratome sections from aldehyde-fixed cerebellum were incubated in N-[acetyl-3H] WGA or WGA conjugated to horseradish peroxidase (WGA-HRP). Sections from this in vitro binding paradigm and those from cerebellar pressure injection eases using those tracers (in vivo binding paradigm) were processed for light microscopic autoradiography, histochemistry, and electron microscopy. Blocking experiments were also performed with various sugar haptens to confirm the binding specificity of these lectin preparations. Light microscopy of lectin binding patterns within the cerebellar cortex has revealed that both derivatized WGA preparations bind most intensely to the molecular layer. Within the deep cerebellar nuclei, binding is unique and produces a punctate delineation of cell bodies and dendrites. Electron microscopy revealed that these binding sites are associated with glial processes which abut the plasma membrane of deep nuclei cells. Cerebellar WGA-HRP injection sites contain labeled profiles involved in uptake and axonal transport of the labeled lectin (e.g., multivesicular and dense bodies) in addition to label associated with synapses, glia, undetermined components of the extracellular space, and neuronal plasma membranes. These sites are therefore presumed to possess a high affinity or capacity for binding derivatized WGA. Binding studies performed here thus reveal, for the first time, the existence of discrete glial sites that display an extraordinary attraction for lectins such as WGA. The roles such glial glycoconjugates play in diverse biological activities including neuronal uptake and transport of macromolecules need further study.Keywords
This publication has 49 references indexed in Scilit:
- Presynaptic neurones may contribute a unique glycoprotein to the extracellular matrix at the synapseNature, 1985
- Tracer uptake by photoreceptor synaptic terminalsJournal of Ultrastructure Research, 1983
- Synaptic membrane domains in photoreceptors of chick retina: a thin-section and a freeze-fracture studyJournal of Ultrastructure Research, 1983
- Localization of axonally transported 125I-wheat germ agglutinin beneath the plasma membrane of chick retinal ganglion cells.The Journal of cell biology, 1983
- Sonication-enhanced histochemistry of wheat germ agglutinin binding to intracellular sites of rat layer V cortical neurons and spinal motoneuronsJournal of Neuroscience Research, 1982
- A light and electron microscopic study of the intraneuronal transport of horseradish peroxidase and wheat germ agglutinin-peroxidase conjugates in the rat visual systemJournal of Neurocytology, 1981
- Lectin cytochemistry of carbohydrates on cell membranes of rat cerebellumJournal of Neurocytology, 1981
- Anatomical evidence for collateral branching of substantia nigra neurons: a combined horseradish peroxidase and [3H]wheat germ agglutinin axonal transport study in the ratBrain Research, 1980
- Electron microscopic observations of horseradish peroxidase transported from the caudoputamen to the substantia nigra in the rat: Possible involvement of the agranular reticulumBrain Research, 1975
- Examination of the topography of the saccharide binding sites of concanavalin A and of the forces involved in complexationBiochemistry, 1970