30 nM siRNA were efficienctly transfected into primary mouse hippocampal neurons with NeuroMag transfection reagent.
This paper shows the high efficiency of NeuroMag transfection reagent from OZ Biosciences to silence gene expression into primary hippocampal neurons using siRNA.paper reference: Proc Natl Acad Sci U S A. 2013 Apr 25.
Modulation of the endoplasmic reticulum-mitochondria interface in Alzheimer's disease and related models.Hedskog L, Pinho CM, Filadi R, Rönnbäck A, Hertwig L, Wiehager B, Larssen P, Gellhaar S, Sandebring A, Westerlund M, Graff C, Winblad B, Galter D, Behbahani H, Pizzo P, Glaser E, Ankarcrona M.
Abstract
It is well-established that subcompartments of endoplasmic reticulum (ER) are in physical contact with the mitochondria. These lipid raft-like regions of ER are referred to as mitochondria-associated
ER membranes (MAMs), and they play an important role in, for example,
lipid synthesis, calcium homeostasis, and apoptotic signaling.
Perturbation of MAM function has previously been suggested in Alzheimer's disease
(AD) as shown in fibroblasts from AD patients and a neuroblastoma cell
line containing familial presenilin-2 AD mutation. The effect of AD
pathogenesis on the ER-mitochondria interplay in the brain has so far remained unknown. Here, we studied ER-mitochondria contacts in human AD brain and related AD mouse and neuronal cell models.
We found uniform distribution of MAM in neurons. Phosphofurin acidic
cluster sorting protein-2 and σ1 receptor, two MAM-associated proteins,
were shown to be essential for neuronal survival, because siRNA
knockdown resulted in degeneration. Up-regulated MAM-associated proteins
were found in the AD brain and amyloid precursor protein (APP)Swe/Lon mouse model, in which up-regulation was observed before the appearance of plaques. By studying an ER-mitochondria
bridging complex, inositol-1,4,5-triphosphate
receptor-voltage-dependent anion channel, we revealed that nanomolar
concentrations of amyloid β-peptide increased
inositol-1,4,5-triphosphate receptor and voltage-dependent anion channel
protein expression and elevated the number of ER-mitochondria contact points and mitochondrial calcium concentrations. Our data suggest an important role of ER-mitochondria contacts and cross-talk in AD pathology.
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