The mushroom bodies are paired neuropils in the insect brain that act as mu
ltimodal sensory integration centers and are involved in learning and memor
y. Our studies, by using 5-bromo-2-deoxyuridine incorporation and the Feulg
en technique, show that immediately before pupation, the brain of the devel
oping honey bee (Apis mellifera) contains approximately 2,000 neuroblasts d
evoted to the production oft;he mushroom body intrinsic neurons (Kenyon cel
ls). These neuroblasts are descended from four clusters of 45 or fewer neur
oblasts each already present in the newly hatched larva. Subpopulations of
Kenyon cells, distinct in cytoarchitecture, position, and immunohistochemic
al traits, are born at different, but overlapping, periods during the devel
opment of the mushroom bodies, with the final complement of these neurons i
n place by the mid-pupal stage. The mushroom bodies of the adult honey bee
have a concentric arrangement of Kenyon cell types, with the outer layers b
orn first and pushed to the periphery by later born neurons that remain nea
rer the center of proliferation. This concentricity is further reflected in
morphologic and immunohistochemical traits of the adult neurons, and is de
monstrated clearly by the pattern of expression of Drosophila myocyte enhan
cer factor 2 (DMEF2)-like immunoreactivity. This is the first comprehensive
study of larval and pupal development of the honey bee mushroom bodies. Si
milarities to patterns of neurogenesis observed in the mushroom bodies of o
ther insects and in the vertebrate cerebral cortex are discussed. (C) 1999
Wiley-Liss, Inc.