The cerebellar Golgi cells of mouse, teleost fish, primate and human specie
s have been studied by means of light and Golgi light microscopic technique
s, confocal laser scanning microscopy. slicing technique, ethanol-cryofract
uring and freeze-fracture methods for scanning electron microscopy and ultr
athin sectioning and freeze-etching replicas for transmission electron micr
oscopy. The Golgi cells appeared in the granular layer as polygonal, stella
te, round or fusiform macroneurons surrounded by the granule cell groups. T
hey exhibited ascending dendrites toward the molecular layer and horizontal
dendrites and a short beaded axonal plexus confined to the granular layer.
Scanning electron microscopy revealed their three-dimensional neuronal geo
metry and smooth outer surfaces. Freeze-fracture method for SEM showed the
stereospatial cytoplasmic arrangement of endoplasmic reticulum, cell organe
lles and nuclear envelope. By means of transmission electron microscopy the
asymmetric synaptic connections of Golgi cell horizontal dendrites -with m
ossy fiber rosettes at the cerebellar glomerulus- and of Golgi cell axons -
with granule cell dendrites at the periphery of glomerular region- were ide
ntified. At the molecular layer, Golgi cell ascending dendrites exhibited s
hort neckless spines establishing asymmetric contacts with granule cell axo
ns or parallel fibers. Shaft asymmetric axodendritic and axospinodendritic
contacts between Golgi cell dendrites and climbing fibers were also found i
n the molecular layer.