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Frameworks of analysis for the neural representation of animate objects and actions
Abstract
A variety of cell types exist in the temporal cortex providing high-level visual descriptions of bodies and their movements. We have investigated the sensitivity of such cells to different viewing conditions to determine the frame(s) of reference utilized in processing. The responses of the majority of cells in the upper bank of the superior temporal sulcus (areas TPO and PGa) found to be sensitive to static and dynamic information about the body were selective for one perspective view (e.g. right profile, reaching right or walking left). These cells can be considered to provide viewer-centred descriptions because they depend on the observer’s vantage point. Viewer-centred descriptions could be used in guiding behaviour. They could also be used as an intermediate step for establishing view-independent responses of other cell types which responded to many or all perspective views selectively of the same object (e.g. head) or movement. These cells have the properties of object-centred descriptions, where the object viewed provides the frame of reference for describing the disposition of object parts and movements (e.g. head on top of shoulders, reaching across the body, walking forward ‘following the nose’). For some cells in the lower bank of the superior temporal sulcus (area TEa) the responses to body movements were related to the object or goal of the movements (e.g. reaching for or walking towards a specific place). This goal-centred sensitivity to interaction allowed the cells to be selectively activated in situations where human subjects would attribute causal and intentional relationships.
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Citations
Cites
Gray, C. M., König, P., Engel, A. K., & Singer, W. (1989) · Nature · doi:10.1038/338334a0 · Cited by 4,183
Cited by
Rizzolatti, G., & Craighero, L. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144230 · Cited by 7,433
Action recognition in the premotor cortex
Gallese, V., Fadiga, L., Fogassi, L., & Rizzolatti, G. (1996) · Brain · doi:10.1093/brain/119.2.593 · Cited by 4,968
Premotor cortex and the recognition of motor actions
Rizzolatti, G., Fadiga, L., Gallese, V., & Fogassi, L. (1996) · Cognitive Brain Research · doi:10.1016/0926-6410(95)00038-0 · Cited by 4,870
Understanding motor events: a neurophysiological study
di Pellegrino, G., Fadiga, L., Fogassi, L., Gallese, V., & Rizzolatti, G. (1992) · Experimental Brain Research · doi:10.1007/bf00230027 · Cited by 3,539
Neurophysiological mechanisms underlying the understanding and imitation of action
Rizzolatti, G., Fogassi, L., & Gallese, V. (2001) · Nature Reviews Neuroscience · doi:10.1038/35090060 · Cited by 3,302
Mirror neurons and the simulation theory of mind-reading
Gallese, V (1998) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(98)01262-5 · Cited by 3,201
Cattaneo, L., & Rizzolatti, G. (2009) · Archives of Neurology · doi:10.1001/archneurol.2009.41 · Cited by 3,137
Rizzolatti, G., & Arbib, M. A. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01260-0 · Cited by 2,858
Social perception from visual cues: Role of the STS region
Allison, T., Puce, A., & McCarthy, G. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01501-1 · Cited by 2,461
A differential neural response in the human amygdala to fearful and happy facial expressions
Morris, J. S., Frith, C. D., Perrett, D. I., Rowland, D., Young, A. W., Calder, A. J., & Dolan, R. J. (1996) · Nature · doi:10.1038/383812a0 · Cited by 2,013
Self-citationNeural mechanisms of empathy in humans: a relay from neural systems for imitation to limbic areas
Carr, L., Iacoboni, M., Dubeau, M.-C., Mazziotta, J. C., & Lenzi, G. L. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0935845100 · Cited by 1,978
Parietal Lobe: From Action Organization to Intention Understanding
Fogassi, L., Ferrari, P. F., Gesierich, B., Rozzi, S., Chersi, F., & Rizzolatti, G. (2005) · Science · doi:10.1126/science.1106138 · Cited by 1,990
The functional role of the parieto-frontal mirror circuit: interpretations and misinterpretations
Rizzolatti, G., & Sinigaglia, C. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2805 · Cited by 1,680
Imitation, empathy, and mirror neurons
Iacoboni, M. (2009) · Annual Review of Psychology · doi:10.1146/annurev.psych.60.110707.163604 · Cited by 1,606
Baron-Cohen, S., Ring, H. A., Bullmore, E. T., Wheelwright, S., Ashwin, C., & Williams, S. C. R. (2000) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(00)00011-7 · Cited by 1,130
Grafton, S., Arbib, M., Fadiga, L., & Rizzolatti, G. (1996) · Experimental Brain Research · doi:10.1007/bf00227183 · Cited by 1,045
Mapping motor representations with positron emission tomography
Decety, J., Perani, D., Jeannerod, M., Bettinardi, V., Tadary, B., Woods, R., Mazziotta, J. C., & Fazio, F. (1994) · Nature · doi:10.1038/371600a0 · Cited by 976
Shape representation in the inferior temporal cortex of monkeys
Logothetis, N. K., Pauls, J., & Poggio, T. (1995) · Current Biology · doi:10.1016/s0960-9822(95)00108-4 · Cited by 963
Neural mechanisms for the recognition of biological movements
Giese, M. A., & Poggio, T. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1057 · Cited by 955
Brain activity during observation of actions. Influence of action content and subject's strategy
Decety, J. (1997) · Brain · doi:10.1093/brain/120.10.1763 · Cited by 942
Organization and functions of cells responsive to faces in the temporal cortex
Perrett, D. I., Hietanen, J. K., Oram, M. W., & Benson, P. J. (1992) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1992.0003 · Cited by 882
Self-citationMurata, A., Gallese, V., Luppino, G., Kaseda, M., & Sakata, H. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.5.2580 · Cited by 841
Ventral intraparietal area of the macaque: congruent visual and somatic response properties
Duhamel, J.-R., Colby, C. L., & Goldberg, M. E. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.1.126 · Cited by 789
The power of simulation: Imagining one's own and other's behavior
Decety, J., & Grèzes, J. (2006) · Brain Research · doi:10.1016/j.brainres.2005.12.115 · Cited by 790
Neural Circuits Involved in the Recognition of Actions Performed by Nonconspecifics: An fMRI Study
Buccino, G., Lui, F., Canessa, N., Patteri, I., Lagravinese, G., Benuzzi, F., Porro, C. A., & Rizzolatti, G. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/089892904322755601 · Cited by 762
Electrophysiology and brain imaging of biological motion
Puce, A., & Perrett, D. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1221 · Cited by 693
Self-citationMind Blindness and the Brain in Autism
Frith, U. (2001) · Neuron · doi:10.1016/s0896-6273(01)00552-9 · Cited by 637
Mirror neurons: from origin to function
Cook, R., Bird, G., Catmur, C., Press, C., & Heyes, C. (2014) · Behavioral and Brain Sciences · doi:10.1017/s0140525x13000903 · Cited by 647
Extrastriate body area in human occipital cortex responds to the performance of motor actions
Astafiev, S. V., Stanley, C. M., Shulman, G. L., & Corbetta, M. (2004) · Nature Neuroscience · doi:10.1038/nn1241 · Cited by 629
Demystifying social cognition: a Hebbian perspective
Keysers, C., & Perrett, D. I. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.09.005 · Cited by 592
Self-citationMotor functions of the parietal lobe
Fogassi, L., & Luppino, G. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.10.015 · Cited by 488
Defining the broader phenotype of autism: genetic, brain, and behavioral perspectives
DAWSON, G., WEBB, S., SCHELLENBERG, G. D., DAGER, S., FRIEDMAN, S., AYLWARD, E., & RICHARDS, T. (2002) · Development and Psychopathology · doi:10.1017/s0954579402003103 · Cited by 467
Pelphrey, K. A., Morris, J. P., & McCarthy, G. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/0898929042947900 · Cited by 454
Iacoboni, M., Lieberman, M. D., Knowlton, B. J., Molnar-Szakacs, I., Moritz, M., Throop, C. J., & Fiske, A. P. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.11.013 · Cited by 459
Cortical connections of the macaque anterior intraparietal (AIP) area
Borra, E., Belmalih, A., Calzavara, R., Gerbella, M., Murata, A., Rozzi, S., & Luppino, G. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm146 · Cited by 402
Towards a unifying neural theory of social cognition
Keysers, C., & Gazzola, V. (2006) · Progress in Brain Research · doi:10.1016/s0079-6123(06)56021-2 · Cited by 367
Integrating automatic and controlled processes into neurocognitive models of social cognition
Satpute, A. B., & Lieberman, M. D. (2006) · Brain Research · doi:10.1016/j.brainres.2006.01.005 · Cited by 347
View-Based Encoding of Actions in Mirror Neurons of Area F5 in Macaque Premotor Cortex
Caggiano, V., Fogassi, L., Rizzolatti, G., Pomper, J. K., Thier, P., Giese, M. A., & Casile, A. (2011) · Current Biology · doi:10.1016/j.cub.2010.12.022 · Cited by 223
Neurophysiology of shape processing
Perrett, D. I., & Oram, M. W. (1993) · Image and Vision Computing · doi:10.1016/0262-8856(93)90011-5 · Cited by 213
Self-citationSimilarities and differences in perceiving threat from dynamic faces and bodies. An fMRI study
Kret, M. E., Pichon, S., Grèzes, J., & de Gelder, B. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.08.012 · Cited by 204
A neurobiological mapping of theory of mind
Abu-Akel, A. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(03)00190-5 · Cited by 189
A Kendama Learning Robot Based on Bi-directional Theory
Miyamoto, H., Schaal, S., Gandolfo, F., Gomi, H., Koike, Y., Osu, R., Nakano, E., Wada, Y., & Kawato, M. (1996) · Neural Networks · doi:10.1016/s0893-6080(96)00043-3 · Cited by 171
Lloyd, D. M. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.09.007 · Cited by 128
Metadata
- Authors
- Perrett, D. I., Harries, M. H., Bevan, R., Thomas, S., Benson, P. J., Mistlin, A. J., Chitty, A. J., Hietanen, J. K., & Ortega, J. E.
- Venue
- Journal of Experimental Biology
- Publisher
- The Company of Biologists
- Published
- 1989-09-01
- Volume
- 146
- Issue
- 1
- Pages
- 87-113
- ISSN
- 0022-0949 (ISSN-L)
- 1477-9145
- OpenAlex
- W1892030233
- Cited by
- 616
- References
- 1
- FWCI
- 13.06
- Type
- journal article
- Language
- en
- Open access
- closed
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