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Islands of Calleja

The islands of Calleja are a group of neural granule cells located within the ventral striatum in the brains of most animals. This region of the brain is part of the limbic system, where it aids in the reinforcing effects of reward-like activities. Within most species, the islands are specifically located within the olfactory tubercle; however, in primates, these islands are located within the nucleus accumbens, the reward center of the brain, since the olfactory tubercle has practically disappeared in the brains of primates. Both of these structures have been implicated in the processing of incentives as well as addictions to drugs. Projections to and from the islands supplement this knowledge with their involvement in the reward pathways for both cocaine and amphetamines.

Location
The islands of Calleja are specifically located within the ventral and medial lining of the ventral striatum in the brain, meaning that they lie towards the front and middle of this region within the temporal lobe. The insula magna, or the major island, of these complexes is located in the medial border of the nucleus accumbens. The ventral group of the islands lies along the pial border of the basal forebrain, a region of the frontal lobe that lies adjacent to the temporal lobe. ==Etymology==
Etymology
The islands of Calleja are named after Julián Calleja y Sánchez, the Spanish anatomist, who studied the structure prior to publishing a paper in 1893 entitled "La región olfatoria del cerebro" ("The olfactory region of the brain"). Although the structure was named after him, Calleja was not the first to study it. Sigbert Ganser, a German psychiatrist, published a paper in 1882 that discussed the region. ==Neurogenesis of neurons in the islands of Calleja==
Neurogenesis of neurons in the islands of Calleja
Sub-ventricular zone Originating from the lateral ganglionic eminence, one of the three embryonic structures that eventually become specific parts of the brain, the sub-ventricular zone (SVZ) is a group of cells that develop along the surface of the ventricular layer of the brain, following the creation of the cortical plate in embryos. The cells generated from this region migrate either radially along or tangentially to radial glia, the cells that help guide neurons to their targeted destination. These progenitors from the SVZ are best known for their migration down the rostral migratory stream to differentiate into the different cells of the olfactory bulb. However, a separate mass of cells, referred to as the "ventral migratory mass," migrates from the SVZ to the basal forebrain, where it develops into the islands of Calleja. ==Structure and neuronal pathways==
Structure and neuronal pathways
In rodents, the islands of Calleja are composed of seven distinct clusters within the olfactory tubercle, with the major island creating a border between the septum, the nucleus accumbens, and the diagonal band. Some of the islands contain a "core" of neuropil, or unmyelinated axons and dendrites, filled with a large cell in some cases. Projections to and from the islands connect the structures to the piriform cortex, which is responsible for processing smell, as well as areas of the basal forebrain, a region responsible for determining an animal's level of wakefulness. The projections with the piriform cortex align with the rest of the olfactory system, the path beginning in the sensory cells of the nose and then proceeding through the olfactory bulb to regions such as the piriform cortex, olfactory tubercle, and amygdala. However, the projections to the basal forebrain structures actually originate from the smaller outer cells of the island clusters as opposed to the large cells within the "core." The islands of Calleja receive inputs from the back of the amygdala, which processes emotional memory, as well as the septum, nucleus accumbens, and piriform cortex. The islands also receive information in the form of dopamine from the substantia nigra and ventral tegmental area, located in the midbrain of the brainstem. Information traveling from these midbrain structures is triggered in response to rewarding activities or feelings. The islands project to the back of the thalamus, a region with many responsibilities such as sensory information processing, regulation of wakefulness, and relaying information to the cerebral cortex. ==Receptor proteins==
Receptor proteins
Bcl-2: The cells within the islands of Calleja that contain the Bcl-2 marker exhibit neuronal immaturity. They are numerous in the islands and are thought to aid in developing pathways for specific response. • Cannabinoid receptor CB2: The cannabinoid receptors are a class of G protein-coupled receptors that bind either internally or externally produced cannabinoids. The CB2 variant was initially believed to be involved only with the cells in the immune system; however, they have been identified in the islands of Calleja and other structures of the limbic system, supporting the idea that this receptor has a neuronal function as well. This function has yet to be determined though. While the CB1 variant of the receptor has a pre-synaptic localization, it is thought that the CB2 receptors may possess a post-synaptic localization. • Dopamine receptor D2: The islands of Calleja are different from other regions in the ventral striatum in that they actually exhibit no expression of this receptor. • Dopamine receptor D3: These specific dopamine receptors exhibit different effects on cells depending on their location in the brain. In the islands of Calleja, their presence inversely affects an animal's interest in an unfamiliar area and the animal's tendency to form addictions. These receptors also contribute to the hypothermic response associated with a lowered room temperature in response to the drug Ecstasy. • Muscarinic acetylcholine receptor M4: The muscarinic acetylcholine receptors are types of G protein-coupled receptors that regulate the effects of acetylcholine on the nervous system. In rodents, the core of the individual islands of Calleja contains high concentrations of the M4 receptor, whereas the peripheral granule cell clusters have lower concentrations, allowing each island to be easily visualized by staining for this specific receptor. The composition of the M4 receptors in the islands of Calleja in the brains of monkeys is similar to that of rodents; however, many of the islands, besides the major island, do not exhibit a noticeable core structure. • Neurotensin receptor NTS3: Neurotensin is a neurotransmitter/neuromodulator associated with a number of functions, such as responses to pain, temperature, sleep-wake cycles, and dopamine. NTS3 is identical to the sorting protein sortilin and possesses many other functions outside the central nervous system. NTS3 is expressed in areas that also express the neurotensin receptor NTS1, including the islands of Calleja. • Oxytocin receptor: Oxytocin is a molecule that induces maternal behaviors in animals. During childbirth, substantial increases in the expression of this receptor occur in the major island of the islands of Calleja. Furthermore, the extent of the increase depends on the mother's previous maternal experience. These changes within the islands of Calleja are connected to the differences in progesterone and estrogen levels during pregnancy. • Phosphodiesterase 7B: Through the degradation of nucleotides, phosphodiesterases (PDE) produce cyclic adenosine monophosphate (cAMP), a molecule involved in sensory processing, neural plasticity, learning, and memory. Of the different families of phosphodiesterases, the 7B variant is one that bonds most easily to cAMP. Within the islands of Calleja, PDE7B is involved in the expression of the dopamine receptor D3. It may also be associated with transferring chemical information from the islands to other regions of the brain. • Prokineticin: The islands contain the mRNA associated with the PK2 variant of the protein as well as the receptor variant PKR1. This class of proteins and receptors is partially responsible for the neurogenesis of cells in the olfactory bulb and certain reproductive behaviors, such as the hormonal events involved with the reproductive system. • Serotonin 5-HT6 receptor: The serotonin 5-HT6 receptor helps to increase neuronal cAMP production. Within the islands of Calleja and other structures of the striatum, these receptors may play a role in locomotor activity and memory. • Syntrophin-associated serine/ threonine kinase (SAST): Syntrophin is an adaptor protein that connects other signaling proteins to dystrophin, a protein with major associations to muscular dystrophy. The SAST variant SAST124 is found in the islands of Calleja and other regions associated with the islands, such as the sub-ventricular zone and the olfactory bulb. ==Function==
Function
As is the case with many structures of the brain, many of the functions of the islands of Calleja have yet to be confirmed and remain as suggestions. Influences on the cardiovascular system The islands regulate the amount of blood supplied to the ventral pallidum and other surrounding areas by adjusting the degree of dilation of the blood vessels that pass through the islands and the ventral pallidum. This vasodilation is adjusted by the action of nitric oxide. Injection of glutamate into the islands results in decreases in arterial pressure and heart rate, suggesting that the islands are involved to some degree in the regulation of arterial pressure and heart rate. The islands also inhibit the effects of the sympathetic nervous system on the cardiovascular system by responding to changes in pressure. Influences on neurological disorders Changes in behavior due to schizophrenia have been traced back to the high level of D3 dopamine receptors within the islands of Calleja as well as the high concentrations of dopamine passing through them. Damage to the islands due to restricted blood supply has been linked to a condition of amnesia and personality changes. Other behavioral and emotional responses occur as well due to serotonin that interacts with the islands. They also play a role in the reward pathways and processing pheromone inputs from the nose. ==References==
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