Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/34024
Title: Mutant huntingtin impairs the post-Golgi trafficking of brain-derived neurotrophic factor but not its Val66Met polymorphism.
Author: Toro, Daniel del
Canals i Coll, Josep M.
Ginés Padrós, Silvia
Kojima, Masami
Egea Guri, Gustavo
Alberch i Vié, Jordi
Keywords: Corea de Huntington
Malalties del sistema nerviós
Aparell de Golgi
Huntington's chorea
Nervous System Diseases
Golgi apparatus
Issue Date: 6-Dec-2006
Abstract: Brain-derived neurotrophic factor (BDNF) polymorphism is associated with the pathophysiology of several neurodegenerative disorders, including Huntington"s disease. In view ofthese data andthe involvement of huntingtin in intracellular trafficking, we examined the intracellular transport and release of Val66Val BDNF (Val-BDNF) and Val66Met BDNF (Met-BDNF) in transfected striatal knock-in cells expressing wild-type or mutant full-length huntingtin. Colocalization studies with specific markers for endoplasmic reticulum showed no differences between the Val-BDNF and Met-BDNF and were not modified by mutant huntingtin. However, post-Golgi trafficking was altered by mutant huntingtin dependent on the BDNF form. Thus, fluorescence recovery after photobleaching (FRAP) and inverse FRAP analysis showed retention of Met-BDNF inthe Golgi apparatus with respectto Val-BDNF in wild-type cells. Strikingly, mutant huntingtin diminished post-Golgi trafficking of Val-BDNF, whereas Met-BDNF was not modified. Accordingly, a reduction in the number of transport vesicles was only observed in mutant huntingtin cells transfected with Val-BDNF but not Met-BDNF. Moreover, mutant huntingtin severely affectedthe KCl-evoked release of Val-BDNF, although it had little effect on Met-BDNF regulated release. The constitutive release of Val-BDNF or Met-BDNF in mutant cells was only slightly reduced. Interestingly, mutant huntingtin only perturbed post-Golgi trafficking of proteins that follow the regulated secretory pathway (epidermal growth factor receptor or atrial natriuretic factor), whereas it did not change those that follow the constitutive pathway (p75 NTR ). We conclude that mutant huntingtin differently affects intracellular transport and release of Val-BDNF and Met-BDNF. In addition, our findings reveal a new role for huntingtin in the regulation of the post-Golgi trafficking of the regulated secretory pathway.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1523/JNEUROSCI.3873-06.2006
It is part of: Journal of Neuroscience, 2006, vol. 26, num. 49, p. 12748-12757
Related resource: http://dx.doi.org/10.1523/JNEUROSCI.3873-06.2006
URI: http://hdl.handle.net/2445/34024
ISSN: 0270-6474
Appears in Collections:Articles publicats en revistes (Biomedicina)

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