The claustrum is a small bilateral
gray matter structure (comprising roughly 0.25% of the cerebral cortex) located deep to the insular cortex and extreme capsule, and superficial to the external capsule and basal ganglia. though a meeting in 2019 of experts has posited a framework by which to refer to the structures across species. However, later work has suggested the claustrum has extensive connections to cortical and subcortical regions. More specifically,
electrophysiological studies show extensive connections to
thalamic nuclei and the
basal ganglia, while isotopological reports have linked the claustrum with the prefrontal, frontal, parietal, temporal and occipital cortices. Additional studies have also looked at the relationship of the claustrum to well-described subcortical white matter tracts. Structures such as the
corona radiata,
occipitofrontal fasciculus and
uncinate fasciculus project to the claustrum from frontal, pericentral, parietal and occipital regions. Reciprocal connections also exist with motor,
somatosensory,
auditory and visual cortical regions. Even with this extensive connectivity, most projections to and from the claustrum are ipsilateral (although there are still contralateral projections), and little evidence exists to describe its afferent or efferent connections with the brainstem and spinal cord. In summary, the cortical and subcortical connectivity of the claustrum implies that it is most involved with processing sensory information, as well as the physical and emotional state of an animal.
Microanatomy Inputs to the claustrum are organized by modality, which include prefrontal, visual, auditory and
somatomotor processing areas. In the same way that the morphology of neurons in the
Rexed laminae of the
spinal cord is indicative of function, the visual, auditory and somatomotor regions within the claustrum share similar neurons with specific functional characteristics. For example, the portion of the claustrum that processes visual information (
primarily synthesizing afferent fibers concerned with our peripheral visual field) is comprised by a majority of binocular cells that have "elongated receptive fields and no orientation selectivity". This focus on the peripheral sensory system is not an isolated occurrence, as most sensory afferents entering the claustrum bring peripheral sensory information. Moreover, the claustrum possesses a distinct
topological organization for each sensory modality as well as the dense connectivity it shares with frontal cortices. For example, there is a retinotopic organization within the visual processing area of the claustrum that mirrors that of visual association cortices and V1, in a similar (yet less complicated) manner to the retinotopic conservation within the lateral geniculate nucleus. Local interneurons themselves are connected through both
chemical and
electrical synapses, allowing for widespread and synchronous inhibition of local claustrum circuitry. In recent studies of the claustrum in
mice cortically-projecting excitatory claustrum neurons were found to form synapses across the anteroposterior axis and were biased toward neurons that do not share projection targets, with the possible function of joining the activity of different afferent modules. Finally, many studies show that the claustrum is best distinguished structurally by its prominent plexus of parvalbumin-positive fibers formed by parvalbumin-expressing inhibitory cell types. Several approaches in
mice have been used to assess claustrum cell types, including electrophysiological, morphological, genetic, and connectomic approaches. While no clear consensus has yet been reached regarding the exact number of excitatory cell types, recent studies have suggested that cortically- and subcortically-projecting claustrum neurons are likely distinct and vary along several metrics, such as their intrinsic electrophysiological profiles, afferent projections, and neuromodulatory profiles. == Function ==