Medial prefrontal cortex (A32 and A25) projections in the common marmoset: a subcortical anterograde study

This study was aimed at establishing the subcorticals substrates of the cognitive and visceromotor circuits of the A32 and A25 cortices of the medial prefrontal cortex and their projections and interactions with subcortical complexes in the common marmoset monkey (Callithrix jacchus). The study was primarily restricted to the nuclei of the diencephalon and amygdala. The common marmoset is a neotropical primate of the new world, and the absence of telencephalic gyrus favors the mapping of neuronal fibers. The biotinylated dextran amine was employed as an anterograde tracer. There was an evident pattern of rostrocaudal distribution of fibers within the subcortical nuclei, with medial orientation. Considering this distribution, fibers originating from the A25 cortex were found to be more clustered in the diencephalon and amygdala than those originating in the A32 cortex. Most areas of the amygdala received fibers from both cortices. In the diencephalon, all regions received projections from the A32, while the A25 fibers were restricted to the thalamus, hypothalamus, and epithalamus at different densities. Precise deposits of neuronal tracers provided here may significantly contribute to expand our understanding of specific connectivity among the medial prefrontal cortex with limbic regions and diencephalic areas, key elements to the viscerocognitive process.

Rostro-Caudal Specificity of Corticospinal Tract Projections in Mice

Rostro-caudal specificity of corticospinal tract (CST) projections from different areas of the cortex was assessed by retrograde labeling with fluorogold and retrograde transfection following retro-AAV/Cre injection into the spinal cord of tdT reporter mice. Injections at C5 led to retrograde labeling of neurons throughout forelimb area of the sensorimotor cortex and a region in the dorsolateral cortex near the barrel field (S2). Injections at L2 led to retrograde labeling of neurons in the posterior sensorimotor cortex (hindlimb area) but not the dorsolateral cortex. With injections of biotinylated dextran amine (BDA) into the main sensorimotor cortex (forelimb region), labeled axons terminated selectively at cervical levels. With BDA injections into caudal sensorimotor cortex (hindlimb region), labeled axons passed through cervical levels without sending collaterals into the gray matter and then elaborated terminal arbors at thoracic sacral levels. With BDA injections into the dorsolateral cortex near the barrel field, labeled axons terminated at high cervical levels. Axons from medial sensorimotor cortex terminated primarily in intermediate laminae and axons from lateral sensorimotor cortex terminated primarily in laminae III–V of the dorsal horn. One of the descending pathways seen in rats (the ventral CST) was not observed in most mice.

A brand-new generation of fluorescent nano-neural tracers: biotinylated dextran amine conjugated carbonized polymer dots

We develop a novel fluorescent nano-neural tracer: BDA–CPDs, which can be anterogradely transported within the peripheral nervous system of rats.

Morphometric analysis of feedforward pathways from the primary somatosensory area (S1) of rats

In this report, we used biotinylated dextran amine to anterogradely label individual axons projecting from primary somatosensory cortex (S1) to four cortical areas in rats, namely the secondary somatosensory (S2), the parietal ventral (PV), the perirhinal (PR), and the contralateral S1 (S1c). A major goal was to determine whether axon terminals could be classified on the basis of morphological criteria, such as the shape and density of boutons, and the shape and size of individual terminal arbors. Evidence from reconstruction of isolated axon terminal fragments (n=111) supported a degree of morphological heterogeneity. In particular, morphological parameters associated with the complexity of terminal arbors and the proportion of beaded, en passant boutons (Bp) vs. stalked boutons terminaux (Bt) were found to differ significantly. Two broad groups could be established following a discriminant function analysis across axon fragments. Both groups occurred in all four target areas, possibly consistent with a commonality of presynaptic processing of tactile information in these areas. However, more work is needed to investigate synaptic function at the single bouton level and see how this might be associated with emerging properties in the postsynaptic targets.

Morphometric analysis of feedforward pathways from the primary somatosensory area (S1) of rats

In this report, we used biotinylated dextran amine to anterogradely label individual axons projecting from primary somatosensory cortex (S1) to four cortical areas in rats, namely the secondary somatosensory (S2), the parietal ventral (PV), the perirhinal (PR), and the contralateral S1 (S1c). A major goal was to determine whether axon terminals could be classified on the basis of morphological criteria, such as the shape and density of boutons, and the shape and size of individual terminal arbors. Evidence from reconstruction of isolated axon terminal fragments (n=111) supported a degree of morphological heterogeneity. In particular, morphological parameters associated with the complexity of terminal arbors and the proportion of beaded, en passant boutons (Bp) vs. stalked boutons terminaux (Bt) were found to differ significantly. Two broad groups could be established following a discriminant function analysis across axon fragments. Both groups occurred in all four target areas, possibly consistent with a commonality of presynaptic processing of tactile information in these areas. However, more work is needed to investigate synaptic function at the single bouton level and see how this might be associated with emerging properties in the postsynaptic targets.

Morphometric analysis of feedforward pathways from the primary somatosensory area (S1) of rats

In this report, we used biotinylated dextran amine to anterogradely label individual axons projecting from primary somatosensory cortex (S1) to four cortical areas in rats, namely the secondary somatosensory (S2), the parietal ventral (PV), the perirhinal (PR), and the contralateral S1 (S1c). A major goal was to determine whether axon terminals could be classified on the basis of morphological criteria, such as the shape and density of boutons, and the shape and size of individual terminal arbors. Evidence from reconstruction of isolated axon terminal fragments (n=111) supported a degree of morphological heterogeneity. In particular, morphological parameters associated with the complexity of terminal arbors and the proportion of beaded, en passant boutons (Bp) vs. stalked boutons terminaux (Bt) were found to differ significantly. Two broad groups could be established following a discriminant function analysis across axon fragments. Both groups occurred in all four target areas, possibly consistent with a commonality of presynaptic processing of tactile information in these areas. However, more work is needed to investigate synaptic function at the single bouton level and see how this might be associated with emerging properties in the postsynaptic targets.