For electrophysiology experiment transfection of hippocampal neurons with miRNA was achieved using NeuroMag.
This paper shows the high efficiency of NeuroMag from OZ Biosciences to transfect miRNA into primary rat hippocampal neurons.article reference: Proc Natl Acad Sci U S A. 2014 Apr 21.
Dystroglycan mediates homeostatic synaptic plasticity at GABAergic synapses.
Abstract
Dystroglycan (DG), a
cell adhesion molecule well known to be essential for skeletal muscle
integrity and formation of neuromuscular synapses, is also present at
inhibitory synapses in the central nervous system. Mutations that affect
DG function not only result in muscular dystrophies, but also in severe
cognitive deficits and epilepsy. Here we demonstrate a role of DG
during activity-dependent homeostatic regulation of hippocampal
inhibitory synapses. Prolonged elevation of neuronal activity
up-regulates DG expression and glycosylation, and its localization to
inhibitory synapses. Inhibition of protein synthesis prevents the
activity-dependent increase in synaptic DG and GABAA receptors (GABAARs),
as well as the homeostatic scaling up of GABAergic synaptic
transmission. RNAi-mediated knockdown of DG blocks homeostatic scaling
up of inhibitory synaptic strength, as does knockdown of
like-acetylglucosaminyltransferase (LARGE)-a glycosyltransferase
critical for DG function. In contrast, DG is not required for the
bicuculline-induced scaling down of excitatory synaptic strength or the
tetrodotoxin-induced scaling down of inhibitory synaptic strength. The
DG ligand agrin increases GABAergic synaptic strength in a DG-dependent
manner that mimics homeostatic scaling up induced by increased activity,
indicating that activation of this pathway alone is sufficient to
regulate GABAAR trafficking. These data demonstrate that DG
is regulated in a physiologically relevant manner in neurons and that DG
and its glycosylation are essential for homeostatic plasticity at
inhibitory synapses.
No comments:
Post a Comment