Light experience induces differential asymmetry pattern of GABA- and parvalbumin-positive cells in the pigeon's visual midbrain

Abstract

The formation of functional and morphological asymmetries within the pigeon's tectofugal system depends on left–right differences in visual input during embryonic development. This asymmetric stimulation presumably affects activity-dependent differentiation processes within the optic tectum. Behavioral studies reveal that prehatch light stimulation asymmetry influences both left- and right-hemispheric processes in a differential way. Thus, we have to assume divergent effects on both hemispheres. This study represents an attempt to test the hypothesis that embryonic light asymmetry induces different, cell-type-specific effects in the left and the right optic midbrain. Since it is likely that inhibitory interneurons play a critical role in the establishment of asymmetries, we examined in both sides of the brain the soma sizes of GABA- and parvalbumin- (PV) immunoreactive (ir) cells of the tectum and the magnocellular isthmic nucleus in controls and in dark-incubated animals. No cell size asymmetries of magnocellular isthmic neurons were found in either dark-incubated or control birds. Dark-incubation also prevented the establishment of lateralized differences in GABAergic and PV-positive tectal cells. However, in control birds GABAergic cells displayed larger somata in the left tectum, whereas PV-ir neurons were enlarged within the right tectum. This complementary asymmetry pattern suggests that PV- and GABA-ir tectal cells represent different cellular populations which react differently to visual input. Thus, our data show that visual lateralization does not result from a mere growth promoting effect that enhances differentiation within the behaviorally dominant left side, but is constituted by different cell type-specific circuits which are divergently adjusted in the left and in the right tectum.