A BDNF autocrine loop in adult sensory neurons prevents cell death
@article{Acheson1995ABA, title={A BDNF autocrine loop in adult sensory neurons prevents cell death}, author={Ann L. Acheson and Joanne C Conover and James P. Fandl and Thomas M. Dechiara and Michelle Russell and Anupriya Thadani and Stephen P. Squinto and George D. Yancopoulos and Ronald M. Lindsay}, journal={Nature}, year={1995}, volume={374}, pages={450-453} }
DURING the initial phase of their development, sensory neurons of the dorsal root ganglion (DRG) require target-derived trophic support for their survival1–3, but as they mature they lose this requirement. Because many of these neurons express BDNF (brain-derived neurotrophic factor) messenger RNA4,5, we hypo-thesized that BDNF might act as an autocrine survival factor in adult DRG neurons, thus explaining their lack of dependence on exogenous growth factors. When cultured adult DRG cells were…
705 Citations
TrkB expression and early sensory neuron survival are independent of endogenous BDNF
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- 2000
These studies of sensory neuron development in BDNF‐deficient embryos have demonstrated that endogenous BDNF is neither required for the early survival of these neurons nor for the induction of TrkB expression.
Non target-derived roles of the neurotrophins.
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The BDNF autocrine loop that is proposed to be present in sensory neurons may be representative of a broader phenomenon in the nervous system as a whole, where the balance of neurotrophic support may shift during development from target-derived to paracrine or autocrine modes.
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The use of pharmacological inhibitors of cellular signalling pathways confirmed the importance of the phosphoinositide kinase-3 (PI 3-K) and protein kinase C (PKC) pathways in this neurotrophin-independent neuronal survival.
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It is shown that the rescuing by GDNF requires the presence of endogenous cortical BDNF, implicating a central role of this neurotrophin in the trophic support of axotomized CSNs and a troPHic cross-talk between BDNF and GDNF regarding the maintenance of lesioned CSNs.
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BDNF expressed in adult-born GCs plays a critical role in dendrite development by acting as an autocrine factor and was required for the development of normal density of spines and normal percentage of sp spine containing the postsynaptic marker PSD-95, suggesting autocrine BDNF regulation of synaptogenesis.
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