Literature DB >> 6352867

Morphological diversity of immunocytochemically identified GABA neurons in the monkey sensory-motor cortex.

C R Houser, S H Hendry, E G Jones, J E Vaughn.   

Abstract

GABAergic neurons have been identified in monkey sensory-motor cerebral cortex by light microscopic, immunocytochemical localization of the GABA synthesizing enzyme, glutamic acid decarboxylase (GAD). All GAD-positive neurons are non-pyramidal cells. Their somata are present in all layers and are evenly distributed across layers II-VI of the motor cortex (area 4), but are found in greater concentrations in layers II, IV and VI of all areas of first somatic sensory cortex (SI; areas 3a, 3b and 1-2). GAD-positive puncta (putative axon terminals) are present throughout the sensory-motor cortex, and they are found immediately adjacent to the somata, dendrites and presumptive axon initial segments of GAD-negative pyramidal cells. In addition, they are observed in close approximation to the somata of both large and small GAD-positive neurons. In area 4, the density of puncta is highest in the superficial cortical layers (layers I-III) and gradually declines throughout the deeper layers. In SI, the highest densities of puncta are present in layer IV, while moderately high densities are found in layers I-III and VI. In areas 3a and 3b, the puncta in layers IV and VI are particularly numerous and form foci that exhibit greater density than adjacent regions. GAD-positive neurons with large somata, 15-33 micron in diameter, are present in layers IIIB-VI of all areas. Such cells have many primary dendrites that radiate in all directions. In addition they have axons that ascend either from the superficial aspect of the somata or from primary dendrites, and that exhibit horizontal collateral branches. These neurons closely resemble the large basket cells (Marin-Padilla, 1969; Jones, 1975), and they may give rise to many of the GAD-positive endings surrounding the somata and proximal dendrites of pyramidal cells in layers III-VI. In addition, small GAD-positive somata are present in all layers, but they are most numerous in layers II and IIIA of all areas and in layer IV of SI. The somata and proximal dendrites of these cells vary from a multipolar shape with small, beaded dendrites, found primarily in layer IV, to bitufted and multipolar shapes with larger, smooth dendrites. The diversity of somal sizes and locations, the variety of dendritic patterns, and the different distributions of GAD-positive puncta, all combine to suggest that several different morphological classes of intrinsic neurons comprise the GABA neurons of monkey cerebral cortex.

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Year:  1983        PMID: 6352867     DOI: 10.1007/bf01181527

Source DB:  PubMed          Journal:  J Neurocytol        ISSN: 0300-4864


  36 in total

1.  Diverse types of interneurons generate thalamus-evoked feedforward inhibition in the mouse barrel cortex.

Authors:  J T Porter; C K Johnson; A Agmon
Journal:  J Neurosci       Date:  2001-04-15       Impact factor: 6.167

2.  Classification of fusiform neocortical interneurons based on unsupervised clustering.

Authors:  B Cauli; J T Porter; K Tsuzuki; B Lambolez; J Rossier; B Quenet; E Audinat
Journal:  Proc Natl Acad Sci U S A       Date:  2000-05-23       Impact factor: 11.205

3.  An optogenetic toolbox designed for primates.

Authors:  Ilka Diester; Matthew T Kaufman; Murtaza Mogri; Ramin Pashaie; Werapong Goo; Ofer Yizhar; Charu Ramakrishnan; Karl Deisseroth; Krishna V Shenoy
Journal:  Nat Neurosci       Date:  2011-01-30       Impact factor: 24.884

4.  Late development of the GABAergic system in the human cerebral cortex and white matter.

Authors:  Gang Xu; Kevin G Broadbelt; Robin L Haynes; Rebecca D Folkerth; Natalia S Borenstein; Richard A Belliveau; Felicia L Trachtenberg; Joseph J Volpe; Hannah C Kinney
Journal:  J Neuropathol Exp Neurol       Date:  2011-10       Impact factor: 3.685

5.  Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons.

Authors:  Sofija Andjelic; Thierry Gallopin; Bruno Cauli; Elisa L Hill; Lisa Roux; Sammy Badr; Emilie Hu; Gábor Tamás; Bertrand Lambolez
Journal:  J Neurophysiol       Date:  2008-12-03       Impact factor: 2.714

6.  Cortical action myoclonus due to cortical laminar necrosis.

Authors:  Francesco Cavallieri; Valentina Fioravanti; Sara Contardi; Luca Codeluppi; Franco Valzania
Journal:  Neurol Sci       Date:  2013-09-20       Impact factor: 3.307

7.  Plasticity in the barrel cortex of the adult mouse: effects of peripheral deprivation on GAD-immunoreactivity.

Authors:  E Welker; E Soriano; H Van der Loos
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

8.  Ultrastructure and synaptic relations of neural elements containing glutamic acid decarboxylase (GAD) in the perigeniculate nucleus of the cat. A light and electron microscopic immunocytochemical study.

Authors:  V M Montero; W Singer
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

Review 9.  GABAergic mechanisms in the pathogenesis and treatment of epilepsy.

Authors:  B S Meldrum
Journal:  Br J Clin Pharmacol       Date:  1989       Impact factor: 4.335

Review 10.  GABA neurons in seizure disorders: a review of immunocytochemical studies.

Authors:  C R Houser
Journal:  Neurochem Res       Date:  1991-03       Impact factor: 3.996

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