Petilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex

doi:10.1038/nrn2402

journal article Jul 01, 2008

Petilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex

Nature Reviews Neuroscience Vol. 9 No. 7 pp. 557-568 · Springer Science and Business Media LLC

View at Publisher Save 10.1038/nrn2402

Topics

No keywords indexed for this article. Browse by subject →

References

110

[1]

Somogyi, P., Tamas, G., Lujan, R. & Buhl, E. H. Salient features of synaptic organisation in the cerebral cortex. Brain Res. Brain Res. Rev. 26, 113–135 (1998). 10.1016/s0165-0173(97)00061-1

[2]

Ramón y Cajal, S. Textura del sistema nervioso del hombre y de los vertebrados (Moya, Madrid, 1899). English translation: Histology of the Nervous System of Man and Vertebrates (Oxford Univ. Press, New York, 1995)

[3]

Lorente de Nó, R. La corteza cerebral de ratón. (Primera contribución - La corteza acústica). Trabajos del Laboratorio de Investigaciones Biológicas de la Universidad de Madrid 20, 41–78 (1922). English translation: Fairén, A., Regidor, J. & Kruger, L. The cerebral cortex of the mouse (a first contribution - the “acoustic” cortex). Somatosens. Mot. Res. 9, 3–36 (1992).

[4]

Szentagóthai, J. The neuron network of the cerebral cortex: a functional interpretation. Proc. R. Soc. Lond. B Biol. Sci. 201, 219–248 (1978). 10.1098/rspb.1978.0043

[5]

Fairén, A., DeFelipe, J. & Regidor, J. in Cerebral Cortex vol. 1 Cellular Components of the Cerebral Cortex (eds, Peters, A. & Jones, E. G.) 201–253 (Plenum, New York, 1984).

[6]

Lund, J. S. Anatomical organization of macaque monkey striate visual cortex. Ann. Rev. Neurosci. 11, 253–288 (1988). 10.1146/annurev.ne.11.030188.001345

[7]

Douglas, R. J. & Martin, K. A. C. in The Synaptic Organization of the Brain (ed. Shepherd, G. M.) 459–511 (Oxford Univ. Press, Oxford, 1998).

[8]

Gupta, A., Wang, Y. & Markram, H. Organizing principles for a diversity of GABAergic interneurons and synapses in the neocortex. Science 287, 273–278 (2000). 10.1126/science.287.5451.273

[9]

Lacaille, J. C., Kunkel, D. D. & Schwartzkroin, P. A. in The Hippocampus: New Vistas (eds Chan-Palay, V. & Kohler, C.) 287–305 (Liss, 1989).

[10]

Maccaferri, G. & Lacaille, J. C. Interneuron diversity series: Hippocampal interneuron classifications - making things as simple as possible, not simpler. Trends Neurosci. 26, 564–571 (2003). 10.1016/j.tins.2003.08.002

[11]

Cauli, B. et al. Molecular and physiological diversity of cortical nonpyramidal cells. J. Neurosci. 17, 3894–3906 (1997). 10.1523/jneurosci.17-10-03894.1997

[12]

Kawaguchi, Y. Physiological, morphological, and histochemical characterization of three classes of interneurons in rat neostriatum. J. Neurosci. 13, 4908–4923 (1993). 10.1523/jneurosci.13-11-04908.1993

[13]

Toledo-Rodriguez, M. et al. Correlation maps allow neuronal electrical properties to be predicted from single-cell gene expression profiles in rat neocortex. Cereb. Cortex 14, 1310–1327 (2004). 10.1093/cercor/bhh092

[14]

Kostyuk, P. G. Synaptic mechanism of central inhibition. Prog. Brain Res. 22, 67–85 (1968). 10.1016/s0079-6123(08)63496-2

[15]

Huang, Z. J., Di Cristo, G. & Ango, F. Development of GABA innervation in the cerebral and cerebellar cortices. Nature Rev. Neurosci. 8, 673–686 (2007). 10.1038/nrn2188

[16]

Bayraktar, T., Welker, E., Freund, T. F., Zilles, K. & Staiger, J. F. Neurons immunoreactive for vasoactive intestinal polypeptide in the rat primary somatosensory cortex: morphology and spatial relationship to barrel-related columns. J. Comp. Neurol. 420, 291–304 (2000). 10.1002/(sici)1096-9861(20000508)420:3<291::aid-cne2>3.0.co;2-h

[17]

Porter, J. T. et al. Properties of bipolar VIPergic interneurons and their excitation by pyramidal neurons in the rat neocortex. Eur. J. Neurosci. 10, 3617–3628 (1998). 10.1046/j.1460-9568.1998.00367.x

[18]

Rozov, A., Jerecic, J., Sakmann, B. & Burnashev, N. AMPA receptor channels with long-lasting desensitization in bipolar interneurons contribute to synaptic depression in a novel feedback circuit in layer 2/3 of rat neocortex. J. Neurosci. 21, 8062–8071 (2001). 10.1523/jneurosci.21-20-08062.2001

[19]

Zilberter, Y., Kaiser, K. M. & Sakmann, B. Dendritic GABA release depresses excitatory transmission between layer 2/3 pyramidal and bitufted neurons in rat neocortex. Neuron 24, 979–988 (1999). 10.1016/s0896-6273(00)81044-2

[20]

Scorcioni, R. & Ascoli, G. A. Algorithmic extraction of morphological statistics from electronic archives of neuroanatomy. Lect. Notes Comput. Sci. 2084, 30–37 (2001). 10.1007/3-540-45720-8_4

[21]

Rall, W. Electrophysiology of a dendritic neuron model. Biophys. J. 2, 145–167 (1962). 10.1016/s0006-3495(62)86953-7

[22]

Sholl, D. A. Dendritic organization in the neurons of the visual cortex and motor cortices of the cat. J. Anat. 87, 387–406 (1953).

[23]

Sholl, D. A. The organization of the visual cortex in the cat. J. Anat. 89, 33–46 (1953).

[24]

Cannon, R. C., Wheal, H. V. & Turner, D. A. Dendrites of classes of hippocampal neurons differ in structural complexity and branching patterns. J. Comp. Neurol. 413, 619–633 (1999). 10.1002/(sici)1096-9861(19991101)413:4<619::aid-cne10>3.0.co;2-b

[25]

Li, Y., Brewer, D., Burke, R. E. & Ascoli, G. A. Developmental changes in spinal motoneuron dendrites in neonatal mice. J. Comp. Neurol. 483, 304–317 (2005). 10.1002/cne.20438

[26]

Uylings, H. B. M. & van Pelt, J. Measures for quantifying dendritic arborizations. Netw. Comput. Neural Syst. 13, 397–414 (2002). 10.1088/0954-898x_13_3_309

[27]

Gray, E. G. Axo-somatic and axo-dendritic synapses of the cerebral cortex: an electron microscopic study. J. Anat. 93, 420–433 (1959).

[28]

Colonnier, M. Synaptic patterns on different cell types in the different laminae of the cat visual cortex. An electron microscope study. Brain Res. 9, 268–287 (1968). 10.1016/0006-8993(68)90234-5

[29]

Peters, A., Palay, S. L. & Webster, H. deF. The Fine Structure of the Nervous System. Neurons and their Supporting Cells (Oxford Univ. Press, New York, 1991).

[30]

Gulyás, A. I., Megías, M., Emri, Z. & Freund, T. F. Total number and ratio of excitatory and inhibitory synapses converging onto single interneurons of different types in the CA1 area of the rat hippocampus. J. Neurosci. 19, 10082–10097 (1999). 10.1523/jneurosci.19-22-10082.1999

[31]

Butt, S. J. et al. The temporal and spatial origins of cortical interneurons predict their physiological subtype. Neuron 48, 591–604 (2005). 10.1016/j.neuron.2005.09.034

[32]

Dumitriu, D., Cossart, R., Huang, J. & Yuste, R. Correlation between axonal morphologies and synaptic input kinetics of interneurons from mouse visual cortex. Cereb. Cortex 17, 81–91 (2007). 10.1093/cercor/bhj126

[33]

Sik, A., Ylinen, A., Penttonen, M. & Buzsáki, G. Inhibitory CA1-CA3-hilar region feedback in the hippocampus. Science 265, 1722–1724 (1994). 10.1126/science.8085161

[34]

Sik, A., Penttonen, M., Ylinen, A. & Buzsáki, G. Hippocampal CA1 interneurons: an in vivo intracellular labeling study. J. Neurosci. 15, 6651–6665 (1995). 10.1523/jneurosci.15-10-06651.1995

[35]

Sik, A., Penttonen, M. & Buzsáki, G. Interneurons in the hippocampal dentate gyrus: an in vivo intracellular study. Eur. J. Neurosci. 9, 573–588 (1997). 10.1111/j.1460-9568.1997.tb01634.x

[36]

Jinno, S. et al. Neuronal diversity in GABAergic long-range projections from the hippocampus. J. Neurosci. 27, 8790–8804 (2007). 10.1523/jneurosci.1847-07.2007

[37]

Miyashita, T. & Rockland, K. S. GABAergic projections from the hippocampus to the retrosplenial cortex in the rat. Eur. J. Neurosci. 26, 1193–1204 (2007). 10.1111/j.1460-9568.2007.05745.x

[38]

Tomioka, R. & Rockland, K. S. Long-distance corticocortical GABAergic neurons in the adult monkey white and gray matter. J. Comp. Neurol. 505, 526–538 (2007). 10.1002/cne.21504

[39]

Tamas, G., Somogyi, P. & Buhl, E. H. Differentially interconnected networks of GABAergic interneurons in the visual cortex of the cat. J. Neurosci. 18, 4255–4270 (1998). 10.1523/jneurosci.18-11-04255.1998

[40]

Somogyi, P. & Cowey, A. Combined Golgi and electron microscopic study on the synapses formed by double bouquet cells in the visual cortex of the cat and monkey. J. Comp. Neurol. 195, 547–566 (1981). 10.1002/cne.901950402

[41]

Somogyi, P. & Cowey, A. in Cerebral Ccortex vol. 1 Cellular Components of the Cerebral Cortex (eds Peters, A. & Jones, E. G.) 337–360 (Plenum, New York, 1984).

[42]

White, E. L. Cortical Circuits. Synaptic Organization of the Cerebral Cortex (Birkhauser, Boston, 1989).

[43]

Valverde, F. The organization of area 18 in the monkey: Golgi study. Anat. Embryol. 154, 305–334 (1978). 10.1007/bf00345659

[44]

Ballesteros-Yánez, I. et al. The double bouquet cell in the human cerebral cortex and a comparison with other mammals. J. Comp. Neurol. 486, 344–360 (2005). 10.1002/cne.20533

[45]

Binzegger, T., Douglas, R. J. & Martin, K. A. Stereotypical bouton clustering of individual neurons in cat primary visual cortex. J. Neurosci. 27, 12242–12254 (2007). 10.1523/jneurosci.3753-07.2007

[46]

Tamas, G., Buhl, E. H. & Somogyi, P. Massive autaptic self-innervation of GABAergic neurons in cat visual cortex. J. Neurosci. 17, 6352–6364 (1997). 10.1523/jneurosci.17-16-06352.1997

[47]

Peters, A. & Harriman, K. M. Different kinds of axon terminals forming symmetric synapses with the cell bodies and initial axon segments of layer II/III pyramidal cells. I. Morphometric analysis. J. Neurocytol. 19, 154–174 (1990). 10.1007/bf01217295

[48]

DeFelipe, J., Hendry, S. H., Jones, E. G. & Schmechel, D. Variability in the terminations of GABAergic chandelier cell axons on initial segments of pyramidal cell axons in the monkey sensory-motor cortex. J. Comp. Neurol. 231, 364–384 (1985). 10.1002/cne.902310307

[49]

Somogyi, P. & Klausberger, T. Defined types of cortical interneuron structure space and spike timing in the hippocampus. J. Physiol. 562, 9–26 (2005). 10.1113/jphysiol.2004.078915

[50]

DeFelipe, J. (ed.) J. Neurocytol. 31, 181–416 (2002). 10.1023/a:1024130805813

Showing 50 of 110 references

Cited By

1,290

A dynamic and multimodal framework to define microglial states

Roman Sankowski, Marco Prinz · 2025

Nature Neuroscience

VIP-to-SST Cell Circuit Motif Shows Differential Short-Term Plasticity across Sensory Areas of Mouse Cortex

Jenifer Rachel, Martin Möck · 2025

The Journal of Neuroscience

Volume electron microscopy analysis of synapses in primary regions of the human cerebral cortex

Nicolás Cano-Astorga, Sergio Plaza-Alonso · 2024

Cerebral Cortex

Integrated platform for multiscale molecular imaging and phenotyping of the human brain

Juhyuk Park, Ji Wang · 2024

Science

From Individual to Population: Circuit Organization of Pyramidal Tract and Intratelencephalic Neurons in Mouse Sensorimotor Cortex

Mei Yao, Ayizuohere Tudi · 2024

Research

Spinal Interneurons: Diversity and Connectivity in Motor Control

Mohini Sengupta, Martha W. Bagnall · 2023

Annual Review of Neuroscience

HCN channels at the cell soma ensure the rapid electrical reactivity of fast-spiking interneurons in human neocortex

Viktor Szegedi, Emőke Bakos · 2023

PLOS Biology

40-Hz Auditory Steady-State Responses in Schizophrenia: Toward a Mechanistic Biomarker for Circuit Dysfunctions and Early Detection and Diagnosis

Tineke Grent-'t-Jong, Marion Brickwedde · 2023

Biological Psychiatry

A multimodal cell census and atlas of the mammalian primary motor cortex

Edward M. Callaway, Hong-Wei Dong · 2021

Nature

Cortical interneurons in autism

Anis Contractor, Iryna M. Ethell · 2021

Nature Neuroscience

Robustness to Noise in the Auditory System: A Distributed and Predictable Property

S. Souffi, C. Lorenzi · 2021

eneuro

Modelling the spatial and temporal constrains of the GABAergic influence on neuronal excitability

Aniello Lombardi, Heiko J. Luhmann · 2021

PLOS Computational Biology

Synaptic inhibition in the neocortex: Orchestration and computation through canonical circuits and variations on the theme

Joana Lourenço, Fani Koukouli · 2020

Cortex

Dysregulation of BRD4 Function Underlies the Functional Abnormalities of MeCP2 Mutant Neurons

Yangfei Xiang, Yoshiaki Tanaka · 2020

Molecular Cell

Distinct Laminar and Cellular Patterns of GABA Neuron Transcript Expression in Monkey Prefrontal and Visual Cortices

Samuel J Dienel, Andrew J Ciesielski · 2020

Cerebral Cortex

Interneuron Types as Attractors and Controllers

Gord Fishell, Adam Kepecs · 2020

Annual Review of Neuroscience

Neuronal cell-subtype specificity of neural synchronization in mouse primary visual cortex

Ulf Knoblich, Lawrence Huang · 2019

Nature Communications

Genetic Single Neuron Anatomy Reveals Fine Granularity of Cortical Axo-Axonic Cells

Xiaojun Wang, Jason Tucciarone · 2019

Cell Reports

Developmental diversification of cortical inhibitory interneurons

Christian Mayer, Christoph Hafemeister · 2018

Nature

Development and Functional Diversification of Cortical Interneurons

Lynette Lim, Da Mi · 2018

Neuron

Metrics

1,290

Citations

110

References

Details

Published: Jul 01, 2008
Vol/Issue: 9(7)
Pages: 557-568
License: View

Cite This Article

(2008). Petilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex. Nature Reviews Neuroscience, 9(7), 557-568. https://doi.org/10.1038/nrn2402

Petilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex

You May Also Like