REST/NRSF governs the expression of dense-core vesicle gliosecretion in astrocytes.


Autoria(s): Prada I.; Marchaland J.; Podini P.; Magrassi L.; D'Alessandro R.; Bezzi P.; Meldolesi J.
Data(s)

2011

Resumo

Astrocytes are the brain nonnerve cells that are competent for gliosecretion, i.e., for expression and regulated exocytosis of clear and dense-core vesicles (DCVs). We investigated whether expression of astrocyte DCVs is governed by RE-1-silencing transcription factor (REST)/neuron-restrictive silencer factor (NRSF), the transcription repressor that orchestrates nerve cell differentiation. Rat astrocyte cultures exhibited high levels of REST and expressed neither DCVs nor their markers (granins, peptides, and membrane proteins). Transfection of a dominant-negative construct of REST induced the appearance of DCVs filled with secretogranin 2 and neuropeptide Y (NPY) and distinct from other organelles. Total internal reflection fluorescence analysis revealed NPY-monomeric red fluorescent protein-labeled DCVs to undergo Ca(2+)-dependent exocytosis, which was largely prevented by botulinum toxin B. In the I-II layers of the human temporal brain cortex, all neurons and microglia exhibited the expected inappreciable and high levels of REST, respectively. In contrast, astrocyte REST was variable, going from inappreciable to high, and accompanied by a variable expression of DCVs. In conclusion, astrocyte DCV expression and gliosecretion are governed by REST. The variable in situ REST levels may contribute to the well-known structural/functional heterogeneity of astrocytes.

Identificador

https://serval.unil.ch/?id=serval:BIB_7A9515F0EB54

isbn:1540-8140 (Electronic)

pmid:21536750

doi:10.1083/jcb.201010126

isiid:000290676400012

http://my.unil.ch/serval/document/BIB_7A9515F0EB54.pdf

http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_7A9515F0EB541

Idioma(s)

en

Direitos

info:eu-repo/semantics/openAccess

Fonte

Journal of Cell Biology, vol. 193, no. 3, pp. 537-549

Palavras-Chave #Animals; Astrocytes/metabolism; Brain/metabolism; Exocytosis; Green Fluorescent Proteins/metabolism; Humans; Kinetics; Neuroglia/metabolism; Neurons/metabolism; Neuropeptide Y/metabolism; PC12 Cells; Rats; Repressor Proteins/metabolism; Secretogranin II/metabolism; Secretory Vesicles/metabolism
Tipo

info:eu-repo/semantics/article

article