In a neuroanatomical tour de force, Nimchinsky and colleagues (1999) obtained access to samples of the anterior cingulate cortex (and other cortical regions) from 28 different primate species, from prosimians to anthropoids to great apes to humans. They processed the samples with a Nissl stain to identify neuronal cell bodies in the cerebral cortex, a structure that (generally) consists of six layers. Spindle neurons are a unique type of neuron found in layer Vb in the ACC and frontoinsular cortex of humans. This is nothing new; spindle neurons (also called Von Economo neurons) were first identified in the 19th century by W. Betz (of the eponymous Betz cell fame, I presume) and by Nobel laureate Santiago Ramón y Cajal. What was new in 1999 was the finding that only humans and great apes have spindle neurons.Our lab has investigated the anatomical structure of the Von Economo (spindle) neurons in anterior cingulate and fronto-insular cortex. Based on functional imaging studies of these brain areas and our studies of the expression of neurotransmitter receptors on these cells, we think they participate in fast, intuitive social decision-making. We have found that the Von Economo neurons emerge mainly in the first three years after birth. We also have evidence that in autistic subjects the Von Economo neurons are abnormally located, possibly as a result of a migration defect. This abnormality may be at least partially responsible for defective social intuition in autism.Somehow, the "spindle neuron" meme hasn't caught on like the "mirror neuron" meme. Is it because spindle neurons have been only been described anatomically (not physiologically), while the reverse is true for mirror neurons? Anatomically speaking, do we know much about mirror neurons? Here's what Rizzolatti and Craighero (2004) have to say about them:
Mirror neurons are a particular class of visuomotor neurons, originally discovered in area F5 of the monkey premotor cortex, that discharge both when the monkey does a particular action and when it observes another individual (monkey or human) doing a similar action (Di Pellegrino et al. 1992, Gallese et al. 1996, Rizzolatti et al. 1996a).In the elegantly titled article, The importance of being agranular, Stewart Shipp reviews evidence that approximately 10% of recorded cells in premotor area F5 in the macaque monkey can be classified as mirror neurons. He also points out an interesting conundrum regarding the anatomical organization of motor cortex: it's agranular, meaning it's lacking the granule cell layer (layer IV), the typical termination point for feedforward sensory information. Area 7b (or PF) in the rostral inferior parietal lobule provides the main parietal input to F5. Without going into too many details, it seems the anatomical circuitry of visual input to F5 is pretty complicated. Anyone who studies mirror neurons (or who does fMRI studies of "empathy and the mirror neuron system") should read these two papers:
from Rizzolatti G, Craighero L. (2004). The mirror-neuron system. Annu Rev Neurosci. 27:169-92.
Geyer S, Matelli M, Luppino G, Zilles K. (2000). Functional neuroanatomy of the primate isocortical motor system. Anat Embryol 202:443-74
Shipp S. (2005). The importance of being agranular: a comparative account of visual and motor cortex. Philos Trans R Soc Lond B Biol Sci. 360:797-814.
Gap ad, with mirror neurons by Rizzolatti & Craighero (2004)