Literature DB >> 2576508

Calcium-induced neuronal degeneration: a normal growth cone regulating signal gone awry (?).

S B Kater1, M P Mattson, P B Guthrie.   

Abstract

The neuronal growth cone is involved in neurite elongation, directional pathfinding, and target recognition. These activities are essential for proper assembly of functional circuits within the developing nervous system, for regeneration of functional circuitry following damage, and also, perhaps, for remodeling of the nervous system in response to environmental stimuli. Our studies of both molluscan and mammalian neurons in culture have shown that neurite outgrowth can only proceed when intracellular calcium levels lie within a specific outgrowth-permissive range. Cessation of outgrowth can be induced by a variety of signals normally used for communication within the adult nervous system, including neurotransmitters, and action potentials; all of these signals elevate levels of intracellular calcium above the outgrowth-permissive range. For example, glutamate, whether added to the medium or released from co-cultured entorhinal explants, can selectively inhibit dendritic outgrowth. Conversely, inhibitory neurotransmitters can block the outgrowth-inhibitory effects of glutamate and actually promote expansion of dendritic arbors. Dendritic outgrowth is therefore regulated by a balance between excitatory and inhibitory neurotransmitter activity. Extreme excitatory imbalance in neurotransmitter input to pyramidal neurons causes cell death. Each of these changes in neuroarchitecture is mediated by changes in levels of intracellular calcium. We therefore put forward the hypothesis that key mechanisms which normally control the development and plasticity of neural circuitry, are also involved in neurodegeneration. Local, moderate elevations in calcium result in dendritic pruning. Higher, global elevations in calcium result in cell death. This cell death may serve an important function during normal development; aging may result in the same mechanism being employed pathologically. When intracellular calcium levels are not regulated within normal limits, as may occur in aging, neurodegeneration may occur.

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Year:  1989        PMID: 2576508     DOI: 10.1111/j.1749-6632.1989.tb12514.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  5 in total

1.  Tetrodotoxin prevents motor unit enlargement after partial denervation in rat hindlimb muscles.

Authors:  S L Tam; V Archibald; N Tyreman; T Gordon
Journal:  J Physiol       Date:  2002-09-01       Impact factor: 5.182

2.  Evidence supporting a role for the calcium-sensing receptor in Alzheimer disease.

Authors:  Yvette P Conley; Ankur Mukherjee; Candace Kammerer; Steven T DeKosky; M Ilyas Kamboh; David N Finegold; Robert E Ferrell
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2009-07-05       Impact factor: 3.568

3.  Self-organized criticality in developing neuronal networks.

Authors:  Christian Tetzlaff; Samora Okujeni; Ulrich Egert; Florentin Wörgötter; Markus Butz
Journal:  PLoS Comput Biol       Date:  2010-12-02       Impact factor: 4.475

4.  The formation of multi-synaptic connections by the interaction of synaptic and structural plasticity and their functional consequences.

Authors:  Michael Fauth; Florentin Wörgötter; Christian Tetzlaff
Journal:  PLoS Comput Biol       Date:  2015-01-15       Impact factor: 4.475

Review 5.  Opposing Effects of Neuronal Activity on Structural Plasticity.

Authors:  Michael Fauth; Christian Tetzlaff
Journal:  Front Neuroanat       Date:  2016-06-28       Impact factor: 3.856

  5 in total

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