Literature DB >> 7813680

Morphological characteristics of cultured olfactory bulb cells.

S P Fracek1, L Guo, R Schafer.   

Abstract

Cultured olfactory bulb cells from embryonic mice had ultrastructural characteristics similar to those of many cell types in the intact adult mouse olfactory bulb. Identified cultured cells included mitral/tufted cells, granule cells, short-axon cells, and fibrous and protoplasmic astrocytes. Cultured neurons were found as individual cells, clusters or aggregates. Clusters consisted of a loose array of neurons that appeared to be densely interconnected by neurites. However, few neurites or fascicles emanated from clusters to adjoining areas. Aggregates consisted of many small, usually rounded, neurons piled on top of one larger neuron, or on more than one, with typically many neurites and fascicles projecting to adjacent aggregates, clusters or individual neurons. Neurites of cultured olfactory bulb cells were well developed, and some were several millimeters long. Synapses were very prominent in these cultures, especially in aggregates, clusters, and fascicles. Electron-lucent, dense-core, and coated vesicles were present. Polarity, shape, and length of the long axis (size) of 815 cultured neurons, identified by positive anti-microtubule-associated protein 2 staining, were documented. Cultured neurons varied in size from 9 to 27 microns, with an average size of 16 microns. Elliptical bipolar (35%), triangular multipolar (21%), and round unipolar (15%) were the most common polarity/shape combinations found in culture. Multipolar, triangular, triangular multipolar, and elliptical bipolar cells increased in size with increasing age of culture. The relative proportions of triangular, multipolar, elliptical multipolar, and triangular multipolar cells decreased, whereas the relative proportions of round, unipolar, and round unipolar cells increased with increasing age of culture. These changes in population subtypes and cell size may indicate continued differentiation and maturation of cultured neurons.

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Year:  1994        PMID: 7813680     DOI: 10.1007/bf02738402

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  42 in total

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Authors:  M E Hatten; M Lynch; R E Rydel; J Sanchez; J Joseph-Silverstein; D Moscatelli; D B Rifkin
Journal:  Dev Biol       Date:  1988-02       Impact factor: 3.582

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Authors:  J H McLean; M T Shipley
Journal:  J Neurosci       Date:  1988-10       Impact factor: 6.167

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Authors:  J H Peacock; D F Rush; L H Mathers
Journal:  Brain Res       Date:  1979-06-22       Impact factor: 3.252

4.  Patterns of neuronal differentiation in developing cultures of neonatal mouse cerebellum: a living and silver impregnation study.

Authors:  C D Allerand
Journal:  J Comp Neurol       Date:  1971-06       Impact factor: 3.215

5.  Adhesion of cultured mammalian central nervous system neurons to flame-modified hydrophobic surfaces.

Authors:  J H Lucas; L E Czisny; G W Gross
Journal:  In Vitro Cell Dev Biol       Date:  1986-01

6.  Laminar organization of mitral and tufted cells in the main olfactory bulb of the adult hamster.

Authors:  F Macrides; S P Schneider
Journal:  J Comp Neurol       Date:  1982-07-10       Impact factor: 3.215

7.  Expression of dopaminergic phenotypes in the mouse olfactory bulb induced by the calcitonin gene-related peptide.

Authors:  S Denis-Donini
Journal:  Nature       Date:  1989-06-29       Impact factor: 49.962

8.  [3H]GABA uptake as a marker for cell type in primary cultures of cerebellum and olfactory bulb.

Authors:  D N Currie; G R Dutton
Journal:  Brain Res       Date:  1980-10-20       Impact factor: 3.252

9.  The morphology of the granule cells of the olfactory bulb.

Authors:  J L Price; T P Powell
Journal:  J Cell Sci       Date:  1970-07       Impact factor: 5.285

10.  Astroglial cells provide a template for the positioning of developing cerebellar neurons in vitro.

Authors:  M E Hatten; R K Liem
Journal:  J Cell Biol       Date:  1981-09       Impact factor: 10.539

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