Literature DB >> 2579242

Morphological properties and membrane channels of the growth cones induced in PC12 cells by nerve growth factor.

P H O'Lague, S L Huttner, C A Vandenberg, K Morrison-Graham, R Horn.   

Abstract

Large growth cones were produced in vitro by nerve growth factor (NGF) treatment of multinucleate cells produced by chemical fusion of cells of the neuron-like clone PC12. These endings were studied both at the light microscopic and ultrastructural levels. The activity of ionic channels at growth cones was recorded with intracellular microelectrodes, patch recording of single channels, and whole cone recording from mechanically isolated growth cones. Morphologically, these large growth cones were characterized by the presence of microspikes and filopodia, by the presence of actin demonstrated immunohistochemically, and by the presence of catecholamine fluorescence. At the ultrastructural level they contained a broad spectrum of organelles with a distribution characteristic of neuronal growth cones, including dense core vesicles, abundant smooth membrane cisternae, microtubules, and a filamentous network. The presence of channels capable of generating action potentials was revealed by intracellular microelectrode recording from the growth cone in the presence of locally applied tetraethylammonium (TEA). TEA appeared to block outward current channels that could effectively shunt inward current activated by depolarization. Action potentials elicited by depolarizing current in the presence of TEA could be blocked reversibly by Cd2+, a specific blocker of Ca channels. These action potentials were often followed by a long after-hyperpolarization lasting hundreds of milliseconds. This after-hyperpolarization was similar to that recorded in the cell body of PC12 cells where it appears to be mediated by Ca-activated K current. Single channel recording from outside-out excised patches of membrane from the growth cones perfused with KF revealed the presence of voltage sensitive Na channels, Ca-activated K channels, and K channels resembling delayed rectifier K channels. Macroscopic currents recorded from mechanically isolated growth cones in the "whole cone" configuration showed rapid inward currents at potentials greater than or equal to -40 mV, followed by delayed outward currents at more positive potentials, a finding providing additional evidence for the presence of Na and K channels in growth cones.

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Year:  1985        PMID: 2579242     DOI: 10.1002/jnr.490130120

Source DB:  PubMed          Journal:  J Neurosci Res        ISSN: 0360-4012            Impact factor:   4.164


  16 in total

1.  Selection of transmitter responses at sites of neurite contact during synapse formation between identified leech neurons.

Authors:  S Ching; S Catarsi; P Drapeau
Journal:  J Physiol       Date:  1993-08       Impact factor: 5.182

2.  Neurotrophin regulation of ionic currents and cell size depends on cell context.

Authors:  N T Sherwood; S S Lesser; D C Lo
Journal:  Proc Natl Acad Sci U S A       Date:  1997-05-27       Impact factor: 11.205

3.  Action potentials, macroscopic and single channel currents recorded from growth cones of Aplysia neurones in culture.

Authors:  F Belardetti; S Schacher; S A Siegelbaum
Journal:  J Physiol       Date:  1986-05       Impact factor: 5.182

4.  Nerve growth factor modulates the drug sensitivity of neurotransmitter release from PC-12 cells.

Authors:  S Kongsamut; R J Miller
Journal:  Proc Natl Acad Sci U S A       Date:  1986-04       Impact factor: 11.205

5.  Calcium current in growth balls from isolated Helix aspersa neuronal growth cones.

Authors:  S Marom; D Dagan
Journal:  Pflugers Arch       Date:  1987-08       Impact factor: 3.657

6.  Selective induction of brain type II Na+ channels by nerve growth factor.

Authors:  G Mandel; S S Cooperman; R A Maue; R H Goodman; P Brehm
Journal:  Proc Natl Acad Sci U S A       Date:  1988-02       Impact factor: 11.205

7.  Characterization of sodium currents in mammalian sensory neurons cultured in serum-free defined medium with and without nerve growth factor.

Authors:  G Omri; H Meiri
Journal:  J Membr Biol       Date:  1990-04       Impact factor: 1.843

8.  EGFP-tagged vasopressin precursor protein sorting into large dense core vesicles and secretion from PC12 cells.

Authors:  Bing-Jun Zhang; Mitsuo Yamashita; Ray Fields; Kiyoshi Kusano; Harold Gainer
Journal:  Cell Mol Neurobiol       Date:  2005-06       Impact factor: 5.046

9.  Fluorescent saxitoxins for live cell imaging of single voltage-gated sodium ion channels beyond the optical diffraction limit.

Authors:  Alison E Ondrus; Hsiao-lu D Lee; Shigeki Iwanaga; William H Parsons; Brian M Andresen; W E Moerner; J Du Bois
Journal:  Chem Biol       Date:  2012-07-27

10.  Voltage dependent calcium currents in PC12 growth cones and cells during NGF-induced cell growth.

Authors:  J Streit; H D Lux
Journal:  Pflugers Arch       Date:  1987-05       Impact factor: 3.657

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