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spindle cell

 
Dictionary: spindle cell

n.
A spindle-shaped cell characteristic of certain tumors.


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Medical Dictionary: spindle cell
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n.

A spindle-shaped cell characteristic of certain tumors.

World of the Mind: spindle cells
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The spindle cells are large bipolar-shaped neurons located in layer 5 of the anterior cingulate cortex (Fig. 1). They are characterized by an apicial dendrite extending towards the cortical surface and a basal dendrite extending towards the white matter (Fig. 2). Their shape is distinct from the pyramidal and stellate cells that constitute most of the cortical neurons. Their axon exits at a right angle from the cell body. They were described by the classical neuroanatomists such as Von Economo (1929). My colleagues and I (Nimchinsky et al. 1999) have found that the spindle cells are present only in humans and our closest relatives, the great apes. The concentration of spindle cells is greatest in humans. Chimpanzees have more than gorillas, which have more than orang-utans. There was no evidence of spindle cells in 23 other species of primates and 30 non-primate species including representatives of most of the major mammalian orders. Spindle cells probably originated in the common ancestor of humans and great apes about 10–15 million years ago. The spindle cells are thus a unique phylogenetic specialization within the hominoids. Their size scales with relative brain size and their location in layer 5 implies that they relay the processing of the anterior cingulate cortex to other parts of the brain.

Layer 5 of the mid-cingulate cortex also contains a distinctive type of large neuron, the gigantopyramidal cell, described by Braak (1976). These cells are located just posterior to the spindle cell field, buried in the cingulate sulcus (see Fig. 2). These cells are motor neurons that control the muscles. Ehrsson, Fagergren, and Forssberg (2001) have studied the cingulate motor area containing the gigantopyramidal neurons in functional magnetic resonance imaging (MRI) experiments. In these experiments, the mid-cingulate motor area is strongly activated when the subject performs the precision grip in which the thumb and index finger grasp an object. Only humans and some monkeys and apes can perform the precision grip, and it is necessary for the fine manipulation of objects. The precision grip produces stronger activation of the mid-cingulate motor cortex than the power grip in which all the fingers wrap around the object to be manipulated. The power grip produces stronger activity in the primary motor cortex. Similarly the mid-cingulate cortex is more strongly activated when the subject makes small, precisely controlled movements, while in the primary motor cortex activity increases with the force exerted by the subject. The mental imagery of hand movements also activates the cingulate motor area. The results imply that the mid-cingulate motor cortex contains phylogenetically specialized circuitry for executing the precise manipulation of objects.

Thus the cingulate cortex contains two phylogenetic specializations characteristic of higher primates. The mid-cingulate motor cortex controls precise, volitional hand movements; the anterior cingulate cortex controls thought and adaptive behaviour. The functions of the anterior cingulate cortex are the analogue of precise manipulation in the realm of thought processes. The anterior cingulate cortex is involved in focused problem solving, the recognition of having committed an error, and the initiation of error-correcting behaviour (see Allman et al. 2001). In a meta-analysis of over 100 functional imaging studies, Paus and his colleagues (1998) found that the more difficult the cognitive task, the stronger the activation. The dorsal part of the anterior cingulate cortex is strongly activated when subjects sorted out the correct response from conflicting cues (Bush, Luu, and Posner 2000). The anterior cingulate is also activated by a variety of drive states such as hunger and thirst (Liotti et al. 2001) so that it assesses discrepancies between desired states and the current state of an individual and brings about changes in behaviour that will improve the individual's state.

Posner and Rothbart (1998) have proposed that the anterior cingulate cortex is involved in the maturation of self-control as an individual progresses through life from infancy to adulthood. The anterior cingulate cortex is activated when subjects retrieve episodic memories, i.e. when they engage in tasks that require remembering specific events in the past. The capacity to use past experience as a guide as to how to respond to current events in one's life is an important aspect of the process of developing self-control and behavioural maturation. Posner and Rothbart's maturation hypothesis is also supported by the steady increase in the metabolic activity of the anterior cingulate cortex from childhood to young adulthood (Von Bogaert et al. 1998). In the classic condition of lack of self-control, attention-deficit hyperactivity disorder, subjects presented with the conflicting cue task do not exhibit a response in the anterior cingulate cortex, while this task elicits a strong response in normal subjects (Bush et al. 1999). Finally Lane and his colleagues (1997) found increased activation of the anterior cingulate cortex in individuals with greater social insight. The spindle cells, which appear to arise post-natally, may have a role in all of the slowly maturing functions of the anterior cingulate cortex.

The anterior cingulate is strongly implicated in many neurological and psychiatric disorders. The spindle cells degenerate in Alzheimer's disease and may be related to decline in cognitive functioning. The volume and metabolic activity in the dorsal part of the anterior cingulate cortex is reduced in autistic patients (Haznedar et al. 2000). The volume and metabolic activity in the ventral part of the anterior cingulate cortex is reduced in depressed patients (Drevets et al. 1997). The anterior cingulate cortex is activated in obsessive–compulsive disorder (Rauch et al. 1994), a condition characterized by excessive focus on real or imaginary problems.

Just as the gigantopyramidal cells are the output from mid-cingulate motor cortex controlling precise, volitional movements, the spindle cells may relay to other parts of the brain the processing within the anterior cingulate cortex related to focused problem solving and adaptive responses to new conditions. Von Economo (1929) recognized structural similarities between the anterior cingulate cortex and the classic motor cortex including such features as the well-developed layer 5. This analogy might be extended to the functions of these areas. Motor cortical areas control body movements; the anterior cingulate cortex may control thought processes.



Fig. 1. A spindle cell and large pyramidal cell from layer 5 of human anterior cingulate cortex. The cells have been stained with an antibody to non-phosphorylated neurofilaments.



Fig. 2. The location of the cortex containing spindle cells and the gigantopyramidal cells on the medial side of the human brain.


(Published 2004)

— Atiya Hakeem/John Allman

    Bibliography
  • Allman, J. M., Hakeem, A., Erwin, J. M., Nimchinsky, E., and Hof, P. (2001). 'The anterior cingulate cortex: the evolution of an interface between emotion and cognition'. Annals of the New York Academy of Sciences, 935.
  • Braak, H. (1976). 'A primitive gigantopyramidal field buried in the depth of the cingulate sulcus of the human brain'. Brain Research, 109.
  • Bush, G., Luu, P., and Posner, M. (2000). 'Cognitive and emotional influences in anterior cingulate cortex'. Trends in Cognitive Science, 4.
  • — —  Frazier, J. A., Rauch, S. L., et al. (1999). 'Anterior cingulate cortex dysfunction in attention-deficit/hyperactivity disorder revealed by fMRI and the counting stroop'. Biological Psychiatry, 45.
  • Drevets, W. C., Price, J. L., Thompson, J. R., et al. (1997). 'Subgenual prefrontal cortex abnormalities in mood disorders'. Nature, 386.
  • Ehrsson, H., Fagergren, A., and Forssberg, H. (2001). 'Differential fronto-parietal activation depending of force used in a precision grip task: a fMRI study'. Journal of Neurophysiology, 85.
  • Haznedar, M., Buchsbaum, M., Wei, T.-C., et al. (2000). 'Limbic circuitry in patients with autism spectrum disorders studied with positron emission tomography and magnetic resonance imaging'. American Journal of Psychiatry, 157.
  • Lane, R. D., Reiman, E. M., Axelrod, B., Yun, L. S., Holmes, A., and Schwartz, G. E. (1997). 'Neural correlates of levels of emotional awareness: evidence of an interaction between emotion and attention in the anterior cingulate cortex'. Journal of Cognitive Neuroscience, 10.
  • Lepage, M., Ghaffar, O., Nyberg, L., and Tulving, E. (2000). 'Prefrontal cortex and episodic memory retrieval mode'. Proceedings of the National Academy of Sciences of the USA, 97.
  • Liotti, M., Brannan, S., Egan, G., et al. (2001). 'Brain responses associated with consciousness of breathlessness (air hunger)'. Proceedings of the National Academy of Sciences of the USA, 98.
  • Nimchinsky, E., Gilissen, E., Allman, J. M., Perl, D. P., Erwin, J. M., and Hof, P. R. (1999). 'A neuronal morphologic type unique to humans and great apes'. Proceedings of the National Academy of Sciences of the USA, 96.
  • Paus, T., Koski, L., Caramanos, Z., and Westbury, C. (1998). 'Regional differences in the effects of task difficulty and motor output on blood flow response in the human anterior cingulate cortex: a review of 107 PET activation studies'. Neuro Report, 9.
  • Posner, M., and Rothbart, M. K. (1998). 'Attention, self-regulation and consciousness'. Philosophical Transactions of the Royal Society, Series B, 353.
  • Rauch, S. L., Jenike, M. A., Alpert, N. M., et al. (1994). 'Regional cerebral blood flow measured during symptom provocation in obsessive-compulsive disorder using oxygen 15-labeled carbon dioxide and positron emission tomography'. Archives of General Psychiatry, 51.
  • Van Bogaert, P., Wikler, D., Damhaut, P., Szliwowski, H., and Goldman, S. (1998). 'Regional changes in glucose metabolism during brain development'. Neuroimage, 8.
  • Von Economo, C. (1929). The Cytoarchitectonics of the Human Cerebral Cortex.


Wikipedia: Spindle neuron
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Neuron: Spindle neuron
Spindle neuron - Cartoon of a spindle cell (right) compared to a normal pyramidal cell (left).
Cartoon of a spindle cell (right) compared to a normal pyramidal cell (left).
Location Anterior cingulate cortex and Frontoinsular cortex
Function Global firing rate regulation and regulation of emotional state
Morphology Unique spindle-shaped projection neuron
Presynaptic connections Local input to ACC and FI
Postsynaptic connections Frontal and temporal cortex.

Spindle neurons, also called von Economo neurons (VENs), are a specific class of neurons that participate in signal transmission in the nervous system, and are characterized by a large spindle-shaped soma, gradually tapering into a single apical axon in one direction, with only a single dendrite facing opposite. Whereas other types of neurons tend to have many dendrites, the polar shaped morphology of spindle neurons is unique. They are found in two very restricted regions in the brains of hominids - the family of species comprising humans and other great apes. Spindle cells are also found in the brains of the humpback whales, fin whales, killer whales and sperm whales [1][2], bottlenose dolphin, Risso’s dolphin, beluga whales[3] and in the brains of African and Asian elephants.[4] The name von Economo neuron comes from their discoverer, Constantin von Economo (1876-1931).

Contents

Function of spindle neurons

Spindle neurons are relatively enormous cells that refract waves of neural signals as they are transmitted from one region of the brain to other regions. Spindle neurons have been implicated by scientists as having an important role in many cognitive abilities and disabilities generally unique to humans, ranging from savant perceptiveness and perfect pitch to dyslexia and autism. While rare in comparison to other neurons, spindle neurons are most abundant, and largest, in humans; they have only been found thus far in the anterior cingulate cortex (ACC) and the frontoinsular cortex (FI). They have also been found in the great apes, and more recently in whales and elephants.

Spindle cells appear to play a central role in the development of intelligent behavior and adaptive response to changing conditions and cognitive dissonance. They emerge postnatally and eventually become widely connected with diverse parts of the brain, indicating their essential contributions to the superior capacity of hominids to focus on difficult problems. Evidence of the importance of their role has been established through single-neuron recording, electrical stimulation, and lesion studies.[citation needed]

Evolutionary significance

The observation that spindle neurons only occur in a highly significant group of animals (from a human point of view) has led to speculation that they are of great importance in human evolution and/or brain function. Their restriction (among the primates) to great apes leads to the hypothesis that they developed no earlier than 15-20 million years ago, prior to the divergence of orangutans from the African great apes. The discovery of spindle neurons in diverse whale species[2][3] has led to the suggestion that they are "a possible obligatory neuronal adaptation in very large brains, permitting fast information processing and transfer along highly specific projections and that evolved in relation to emerging social behaviors.".[3]p.254

ACC spindle neurons

In 1999, Professor John Allman, a neuroscientist, and colleagues at the California Institute of Technology first published a report on spindle neurons found in the anterior cingulate cortex (ACC) of hominids, but not in any other species. Neuronal volumes of ACC spindle neurons were larger in humans and the gracile chimpanzees than the spindle neurons of the robust gorillas and orangutans.

Allman and his colleagues have delved beyond the level of brain infrastructure to investigate how spindle neurons function at the superstructural level, focusing on their role as 'air traffic controllers' for emotions. Allman's team reports that spindle neurons help channel neural signals from deep within the cortex to relatively distant parts of the brain.

Specifically, Allman's team found signals from the ACC are received in Brodmann's area 10, in the frontal polar cortex, where regulation of cognitive dissonance (disambiguation between alternatives) is thought to occur. According to Allman, this neural relay appears to convey motivation to act, and concerns the recognition of error. Self-control - and avoidance of error - is thus facilitated by the executive gatekeeping function of the ACC, as it regulates the interference patterns of neural signals between these two brain regions.

In humans, intense emotion activates the anterior cingulate cortex, as it relays neural signals transmitted from the amygdala (a primary processing center for emotions) to the frontal cortex, perhaps by functioning as a sort of lens to focus the complex texture of neural signal interference patterns. The ACC is also active during demanding tasks requiring judgment and discrimination, and when errors are detected by an individual. During difficult tasks, or when experiencing intense love, anger, or lust, activation of the ACC increases. In brain imaging studies, the ACC has specifically been found to be active when mothers hear infants cry, underscoring its role in affording a heightened degree of social sensitivity - a cognitive function at which women are generally more adept than men.

The ACC is a relatively ancient cortical region, is involved with many autonomic functions, including motor and digestive functions, while also playing a role in the regulation of blood pressure and heart rate. Significant olfactory and gustatory capabilities of the ACC and frontoinsular cortex appear to have been usurped, during recent evolution, to serve enhanced roles related to higher cognition - ranging from planning and self awareness to role playing and deception. The diminished olfactory function of humans, compared to other primates, may be related to the fact that spindle cells located at crucial neural network hubs have only two dendrites rather than many, resulting in reduced neurological integration.

Frontoinsular spindle neurons

At a Society for Neuroscience meeting in 2003, Allman reported on spindle cells his team found in another brain region, the frontoinsular cortex, a region which appears to have undergone significant evolutionary adaptations in mankind - perhaps as recently as 100,000 years ago.

This frontoinsular cortex is closely connected to the insula, a region that is roughly the size of a thumb in each hemisphere of the human brain. The insula and frontoinsular cortex are part of the orbitofrontal cortex, wherein the elaborate circuitry associated with spatial awareness and the sense of touch are found, and where self awareness and the complexities of emotion are thought to be generated and experienced. Moreover, this region of the right hemisphere is crucial to navigation and perception of three dimensional rotations.

Spindle neuron concentrations

ACC

The largest number of ACC spindle neurons are found in humans, fewer in the gracile great apes; and fewest in the robust great apes. In both humans and bonobos they are often found in clusters of 3 to 6 neurons. In decreasing order of abundance, they are found in humans, bonobos, common chimpanzees, gorillas, and orangutans. While total quantities of ACC spindle neurons were not reported by Allman in his seminal research report (as they were in a later report describing their presence in the frontoinsular cortex, below), his team's initial analysis of the ACC layer V in hominids revealed an average of ~9 spindle neurons per section for orangutans (rare, 0.6% of section cells), ~22 for gorillas (frequent, 2.3%), ~37 for chimpanzees (abundant, 3.8%), ~68 for bonobos (abundant/clusters, 4.8%), ~89 for humans (abundant/clusters, 5.6%).

Frontoinsula

All of the primates examined had more spindle cells in the frontoinsula of the right hemisphere than in the left. In contrast to the higher number of spindle cells found in the ACC of the gracile bonobos and chimpanzees, the number of frontoinsular spindle cells was far higher in the cortex of robust gorillas (no data for Orangutans was given). An adult human had 82,855 such cells, a gorilla had 16,710, a bonobo had 2,159, and a chimpanzee had a mere 1,808 - despite the fact that chimpanzees and bonobos are great apes most closely related to humans.

Related pathologies

Abnormal spindle neuron development may be linked to several psychotic disorders, typically those characterized by distortions of reality, disturbances of thought, disturbances of language and withdrawal from social contact. Altered spindle neuron states have been implicated in both schizophrenia and Alzheimer's disease, but research into these correlations remains at a very early stage.

Abnormalities in the physiological activity and anatomy of the anterior cingulate cortex are present in most of the major neuropsychiatric disorders. Allman's team has reported reduced ACC size and metabolic activity in autistic patients, as revealed in structural MRI and PET studies, and activity of the ACC is also reduced in patients, mostly boys, diagnosed with attention deficit disorder, characterized by behavioral and learning disorders.[citation needed]

Studies in humans indicate spindle cells are especially vulnerable to degeneration in Alzheimer's disease, with a loss of approximately 60 percent of ACC spindle neurons. Spindle cells also appear to be targeted in frontotemporal dementia.[5]

References

  1. ^ Coghlan A (27 November 2006). "Whales boast the brain cells that 'make us human'". New Scientist. http://www.newscientist.com/article.ns?id=dn10661&print=tru. 
  2. ^ a b Hof PR, Van der Gucht E (Jan 2007). "Structure of the cerebral cortex of the humpback whale, Megaptera novaeangliae (Cetacea, Mysticeti, Balaenopteridae)". Anat Rec (Hoboken) 290 (1): 1–31. doi:10.1002/ar.20407. PMID 17441195. 
  3. ^ a b c Butti C, Sherwood CC, Hakeem AY, Allman JM, Hof PR. (2009). Total number and volume of Von Economo neurons in the cerebral cortex of cetaceans. J Comp Neurol. 515(2):243-59. PMID 19412956
  4. ^ Hakeem AY, Sherwood CC, Bonar CJ, Butti C, Hof PR, Allman JM. (2009). Von Economo neurons in the elephant brain. Anat Rec (Hoboken). 292(2):242-8.PubMed doi:10.1002/ar.20829
  5. ^ Seeley WW, Carlin DA, Allman JM, et al. (Dec 2006). "Early frontotemporal dementia targets neurons unique to apes and humans". Ann Neurol. 60 (6): 660–7. doi:10.1002/ana.21055. PMID 17187353. 

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Dictionary. The American Heritage® Dictionary of the English Language, Fourth Edition Copyright © 2007, 2000 by Houghton Mifflin Company. Updated in 2009. Published by Houghton Mifflin Company. All rights reserved.  Read more
Medical Dictionary. The American Heritage® Stedman's Medical Dictionary Copyright © 2002, 2001, 1995 by Houghton Mifflin Company Read more
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