Literature DB >> 10383119

Are there differences between the secretion characteristics of NGF and BDNF? Implications for the modulatory role of neurotrophins in activity-dependent neuronal plasticity.

O Griesbeck1, M Canossa, G Campana, A Gärtner, M C Hoener, H Nawa, R Kolbeck, H Thoenen.   

Abstract

In previous experiments the activity-dependent secretion of nerve growth factor (NGF) from native hippocampal slices and from NGF-cDNA transfected hippocampal neurons showed unusual characteristics [Blochl and Thoenen (1995) Eur J Neurosci 7:1220-1228; (1996) Mol Cell Neurosci 7:173-190]. In both hippocampal slices and cultured hippocampal neurons the activity-dependent secretion proved to be independent of extracellular calcium, but dependent on the release of calcium from intracellular stores. Under different experimental conditions, Goodman et al. [(1996) Mol Cell Neurosci 7:222-238] reported that the high potassium-mediated secretion of brain-derived neurotrophic factor (BDNF) from hippocampal cultures was dependent on extracellular calcium. Mowla et al. [(1997) Proc 27th Annu Meet Soc Neurosci New Orleans 875.10] reported on even further-reaching differences between NGF and BDNF secretion, namely, that in hippocampal neurons and in pituitary cell lines NGF was secreted exclusively according to the constitutive pathway, whereas BDNF was exclusively sorted according to the activity-dependent regulated pathway. In view of the crucial importance of such potential differences between the processing, sorting, and secretory mechanisms of different neurotrophins for their modulatory roles in activity-dependent neuronal plasticity, a thorough analysis under comparable experimental conditions was mandatory. We demonstrate that in native hippocampal slices and adenoviral-transduced hippocampal neurons there are no differences between NGF and BDNF with respect to the subcellular distribution and mechanism of secretion; that the activity-dependent secretion of both NGF and BDNF is dependent on intact intracellular calcium stores; and that the differences between our own observations and those of Goodman et al. (ibid.) regarding the dependence on extracellular calcium do not reflect differences between NGF and BDNF sorting and secretion, but reflect the differing experimental conditions used.

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Year:  1999        PMID: 10383119     DOI: 10.1002/(SICI)1097-0029(19990515/01)45:4/5<262::AID-JEMT10>3.0.CO;2-K

Source DB:  PubMed          Journal:  Microsc Res Tech        ISSN: 1059-910X            Impact factor:   2.769


  37 in total

1.  Regulated secretion of neurotrophins by metabotropic glutamate group I (mGluRI) and Trk receptor activation is mediated via phospholipase C signalling pathways.

Authors:  M Canossa; A Gärtner; G Campana; N Inagaki; H Thoenen
Journal:  EMBO J       Date:  2001-04-02       Impact factor: 11.598

2.  Effects of early visual experience and diurnal rhythms on BDNF mRNA and protein levels in the visual system, hippocampus, and cerebellum.

Authors:  G S Pollock; E Vernon; M E Forbes; Q Yan; Y T Ma; T Hsieh; R Robichon; D O Frost; J E Johnson
Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

3.  Coordinate action of pre- and postsynaptic brain-derived neurotrophic factor is required for AMPAR trafficking and acquisition of in vitro classical conditioning.

Authors:  W Li; J Keifer
Journal:  Neuroscience       Date:  2008-06-25       Impact factor: 3.590

4.  Bridging the gap between traditional cell cultures and bioreactors applied in regenerative medicine: practical experiences with the MINUSHEET perfusion culture system.

Authors:  Will W Minuth; Lucia Denk
Journal:  Cytotechnology       Date:  2015-04-17       Impact factor: 2.058

5.  Mechanisms of the release of anterogradely transported neurotrophin-3 from axon terminals.

Authors:  XiaoXia Wang; Rafal Butowt; Michael R Vasko; Christopher S von Bartheld
Journal:  J Neurosci       Date:  2002-02-01       Impact factor: 6.167

6.  Calcitonin gene-related peptide enhances release of native brain-derived neurotrophic factor from trigeminal ganglion neurons.

Authors:  Ilya Buldyrev; Nathan M Tanner; Hui-ya Hsieh; Emily G Dodd; Loi T Nguyen; Agnieszka Balkowiec
Journal:  J Neurochem       Date:  2006-10-25       Impact factor: 5.372

7.  Synaptic secretion of BDNF after high-frequency stimulation of glutamatergic synapses.

Authors:  M Hartmann; R Heumann; V Lessmann
Journal:  EMBO J       Date:  2001-11-01       Impact factor: 11.598

8.  Brain-derived neurotrophic factor signal enhances and maintains the expression of AMPA receptor-associated PDZ proteins in developing cortical neurons.

Authors:  Hussam Jourdi; Yuriko Iwakura; Mako Narisawa-Saito; Kyoko Ibaraki; Huabao Xiong; Masahiko Watanabe; Yasunori Hayashi; Nobuyuki Takei; Hiroyuki Nawa
Journal:  Dev Biol       Date:  2003-11-15       Impact factor: 3.582

Review 9.  BDNF signaling in the formation, maturation and plasticity of glutamatergic and GABAergic synapses.

Authors:  Kurt Gottmann; Thomas Mittmann; Volkmar Lessmann
Journal:  Exp Brain Res       Date:  2009-09-24       Impact factor: 1.972

10.  A simple role for BDNF in learning and memory?

Authors:  Carla Cunha; Riccardo Brambilla; Kerrie L Thomas
Journal:  Front Mol Neurosci       Date:  2010-02-09       Impact factor: 5.639

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