Literature DB >> 6493482

Isolation and partial characterisation of neuronal growth cones from neonatal rat forebrain.

P R Gordon-Weeks, R O Lockerbie.   

Abstract

We have devised a method for the isolation of viable neuronal growth cones from neonatal rat forebrain. The method involves differential and density gradient centrifugation and exploits the relatively low buoyant density (approximately 1.018 g/cm3) of growth cones. There are no known biochemical markers for growth cones and it was necessary therefore to monitor for their presence during the isolation using transmission electron microscopy. Several criteria were used to identify isolated growth cones including the presence of filopodia, an extensive system of branching, tubular smooth endoplasmic reticulum and a region rich in microfilaments subjacent to the plasma membrane. These morphological features are similar to those of growth cones identified unequivocally in intact developing brain and in tissue culture. Electron microscopical analysis showed that greater than 90% of membrane-bound, identifiable objects in one fraction were growth cones by these criteria. The major contaminant consisted of membrane sacs and vesicles of unidentified origin. There were only small amounts of isolated rough endoplasmic reticulum and mitochondria. Isolated growth cones were roughly spherical in shape with a diameter of 1.9 +/- 0.5 micron (mean +/- 1 SD). They usually contained mitochondria, large granular vesicles and small vesicles, and occasionally contained coated vesicles, lysosomes, lamellar bodies and multivesicular bodies, and only very rarely, intermediate filaments. Occasionally, growth cones had rudimentary synapses on them. The viability of isolated growth cones was investigated by observing their behaviour in short-term culture. After a few hours in culture on poly-D-lysine-coated coverslips, growth cones flattened down and extended filopodia-like processes. This behaviour was inhibited by cytochalasin B and reversibly by cold (4 degrees C). We conclude that physiologically active growth cones can be isolated rapidly and in large numbers by the method described here.

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Year:  1984        PMID: 6493482     DOI: 10.1016/0306-4522(84)90264-1

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  7 in total

Review 1.  Role of the growth cone in neuronal differentiation.

Authors:  C O Van Hooff; A B Oestreicher; P N De Graan; W H Gispen
Journal:  Mol Neurobiol       Date:  1989 Spring-Summer       Impact factor: 5.590

2.  Characterization of a monoclonal antibody directed against a sulphoglycolipid that is evolutionarily conserved and developmentally regulated in rat brain.

Authors:  E Borroni; E A Derrington; V P Whittaker
Journal:  Cell Tissue Res       Date:  1989       Impact factor: 5.249

3.  Gαz regulates BDNF-induction of axon growth in cortical neurons.

Authors:  Rainbo Hultman; Udhaya Kumari; Nadine Michel; Patrick J Casey
Journal:  Mol Cell Neurosci       Date:  2013-12-07       Impact factor: 4.314

4.  DCX, a new mediator of the JNK pathway.

Authors:  Amos Gdalyahu; Indraneel Ghosh; Talia Levy; Tamar Sapir; Sivan Sapoznik; Yael Fishler; David Azoulai; Orly Reiner
Journal:  EMBO J       Date:  2004-02-05       Impact factor: 11.598

5.  Posttranslational membrane attachment and dynamic fatty acylation of a neuronal growth cone protein, GAP-43.

Authors:  J H Skene; I Virág
Journal:  J Cell Biol       Date:  1989-02       Impact factor: 10.539

Review 6.  Molecular basis of the functions of the mammalian neuronal growth cone revealed using new methods.

Authors:  Michihiro Igarashi
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2019       Impact factor: 3.493

7.  Novel inhibitory action of tunicamycin homologues suggests a role for dynamic protein fatty acylation in growth cone-mediated neurite extension.

Authors:  S I Patterson; J H Skene
Journal:  J Cell Biol       Date:  1994-02       Impact factor: 10.539

  7 in total

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