Ea. Nimchinsky et al., NEUROFILAMENT AND CALCIUM-BINDING PROTEINS IN THE HUMAN CINGULATE CORTEX, Journal of comparative neurology, 384(4), 1997, pp. 597-620
Functional imaging studies of the human brain have suggested the invol
vement of the cingulate gyrus in a wide variety of affective, cognitiv
e, motor, and sensory functions. These studies highlighted the need fo
r detailed anatomic analyses to delineate its many cortical fields mor
e clearly. In the present study, neurofilament protein, and the calciu
m-binding proteins parvalbumin, calbindin, and calretinin were used as
neurochemical markers to study the differences among areas and subare
as in the distributions of particular cell types or neuropil staining
patterns. The most rostral parts of the anterior cingulate cortex were
marked by a lower density of neurofilament protein-containing neurons
, which were virtually restricted to layers V and VI. Immunoreactive l
ayer III neurons, in contrast, were sparse in the anterior cingulate c
ortex, and reached maximal densities in the posterior cingulate cortex
. These neurons were more prevalent in dorsal than in ventral portions
of the gyrus. Parvalbumin-immunoreactive neurons generally had the sa
me distribution. Calbindin- and calretinin-immunoreactive nonpyramidal
neurons had a more uniform distribution along the gyrus. Calbindin-im
munoreactive pyramidal neurons were more abundant anteriorly than post
eriorly, and a population of calretinin-immunoreactive pyramidal-like
neurons in layer V was found largely in the most anterior and ventral
portions of the gyrus. Neuropil labeling with parvalbumin and calbindi
n was most dense in layer III of the anterior cingulate cortex. In add
ition, parvalbumin-immunoreactive axonal cartridges were most dense in
layer V of area 24a. Calretinin immunoreactivity showed less regional
specificity, with the exception of areas 29 and 30. These chemoarchit
ectonic features may represent cellular reflections of functional spec
ializations in distinct domains of the cingulate cortex. (C) 1997 Wile
y-Liss, Inc.