Mints are multimodular adapter proteins in functioning membrane transport a
nd organization. Mint1 and mint2 are neuron-specific. We localized these is
oforms in mouse brain. By in situ hybridization, mRNA encoding mint1 or min
t2 was expressed in neurons throughout the brain. Mint1 mRNA expression was
greatest in the limbic system including cingulate cortex, hippocampus, ant
erior thalamic nuclei, medial habenular nucleus, and mammillary body, Mint2
mRNA was rich in cerebral cortex, entorhinal cortex, and hippocampus, but
less prominent in other limbic structures. Mint1 mRNA and mint2 mRNA were d
istributed among hippocampal pyramidal neurons, while mint2 mRNA was especi
ally abundant in CA3. Mint1, but not Mint2 mRNA was abundant in the substan
tia nigra pars compacta. Immunohistochemistry visualized mint proteins in a
xon terminals and neuronal somata, generally following mRNA distribution. I
n the hippocampus, mint1 was rich in the entorhinal projections and mossy f
ibers of the dentate gyrus, while mint2 was rich in commisural fibers from
the contralateral hippocampus and in CAI. Mint1 intensely stained catechola
mine-containing neurons such as the substantia nigra pars compacta, ventral
tegmental area, and locus ceruleus. Mint2 protein was ubiquitous in these
regions. Mint1 and mint2 distribution also differed elsewhere in the brains
tem and in the cerebellum. Central nervous system neurons, then, predominan
tly express either mint1 or mint2. Mints may be involved in synaptic vesicl
e transport toward the active zone, also participating in transport of cert
ain membrane proteins toward the postsynaptic density. Mint1 and mint2 may
divide roles either regionally or depending on neuronal functional characte
ristics. (C) 2001 Elsevier Science BY All rights reserved.