Literature DB >> 11743966

Filamentous actin is concentrated in specific subpopulations of neuronal and glial structures in rat central nervous system.

F Capani1, M H Ellisman, M E Martone.   

Abstract

This paper is the second in a series of studies on the light and electron microscopic distribution of filamentous actin (F-actin) in the rat central nervous system (CNS) using phalloidin tagged with the fluorophore eosin followed by fluorescence photooxidation. A previous report described the selective localization of high concentrations of F-actin in subpopulations of dendritic spines in hippocampus, cerebellum and neostriatum. Dendritic spines were the most intensely stained structures in the CNS, but several other structures were notable for their consistent staining for F-actin. Although the majority of cell bodies, axons and large dendrites were unlabeled, mossy fibers and Schaffer collaterals in the hippocampal formation, basket cell axons in the cerebellar pinceau, and granule cell dendrites in the glomeruli of the cerebellar cortex routinely showed strong F-actin labeling. Staining was observed in all three glial cell types. Labeling was consistently observed in the astrocytic processes surrounding the Purkinje cell soma and primary dendrite. Intense but sporadic staining was observed in the perinodal glia of the Node of Ranvier. A few examples of labeled oligodendrocyte processes were also seen in the neostriatum. Labeling was observed in microglia in every brain region examined, although the labeling was present in the lumen of the endoplasmic reticulum and the nuclear membrane, leading to questions about its specificity. Perycites apposed to the blood vessels also showed very consistent labeling. Our results suggest that selected structures in the adult CNS in addition to dendritic spines are enriched in F-actin.

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Year:  2001        PMID: 11743966     DOI: 10.1016/s0006-8993(01)03189-4

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  16 in total

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2.  Postsynaptic enrichment of Eps8 at dendritic shaft synapses of unipolar brush cells in rat cerebellum.

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3.  Histochemical localization of caldesmon in the CNS and ganglia of the mouse.

Authors:  Christoph N Köhler
Journal:  J Histochem Cytochem       Date:  2011-03-16       Impact factor: 2.479

4.  Loss of Microtubule-Associated Protein 2 Immunoreactivity Linked to Dendritic Spine Loss in Schizophrenia.

Authors:  Micah A Shelton; Jason T Newman; Hong Gu; Allan R Sampson; Kenneth N Fish; Matthew L MacDonald; Caitlin E Moyer; James V DiBitetto; Karl-Anton Dorph-Petersen; Peter Penzes; David A Lewis; Robert A Sweet
Journal:  Biol Psychiatry       Date:  2015-01-30       Impact factor: 13.382

Review 5.  Receptors, ion channels, and signaling mechanisms underlying microglial dynamics.

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6.  Density of small dendritic spines and microtubule-associated-protein-2 immunoreactivity in the primary auditory cortex of subjects with schizophrenia.

Authors:  Brandon C McKinney; Matthew L MacDonald; Jason T Newman; Micah A Shelton; Rebecca A DeGiosio; Ryan M Kelly; Kenneth N Fish; Allan R Sampson; David A Lewis; Robert A Sweet
Journal:  Neuropsychopharmacology       Date:  2019-02-22       Impact factor: 7.853

7.  Phosphorylation of ezrin/radixin/moesin proteins by LRRK2 promotes the rearrangement of actin cytoskeleton in neuronal morphogenesis.

Authors:  Loukia Parisiadou; Chengsong Xie; Hyun Jin Cho; Xian Lin; Xing-Long Gu; Cai-Xia Long; Evy Lobbestael; Veerle Baekelandt; Jean-Marc Taymans; Lixin Sun; Huaibin Cai
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Journal:  J Comp Neurol       Date:  2009-03-01       Impact factor: 3.215

9.  Drebrin-induced stabilization of actin filaments.

Authors:  Mouna A Mikati; Elena E Grintsevich; Emil Reisler
Journal:  J Biol Chem       Date:  2013-05-21       Impact factor: 5.157

Review 10.  Microglia as therapeutic targets after neurological injury: strategy for cell therapy.

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Journal:  Expert Opin Ther Targets       Date:  2021-06-01       Impact factor: 6.902

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