Proteomics

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CNS-derived extracellular vesicles from superoxide dismutase 1 (SOD1)G93A ALS mice originate from astrocytes and neurons and carry misfolded SOD1


ABSTRACT: Extracellular vesicles (EVs) are secreted by myriad cells in culture and also by unicellular organisms, and their identification in mammalian fluids suggests that EV release also occurs at the organism level. However, although it is clearly important to better understand EVs' roles in organismal biology, EVs in solid tissues have received little attention. Here, we modified a protocol for EV isolation from primary neural cell culture to collect EVs from frozen whole murine and human neural tissues by serial centrifugation and purification on a sucrose gradient. Quantitative proteomics comparing brain-derived EVs from nontransgenic (NTg) and a transgenic amyotrophic lateral sclerosis (ALS) mouse model, superoxide dismutase 1 (SOD1) G93A , revealed that these EVs contain canonical exosomal markers and are enriched in synaptic and RNA-binding proteins. The compiled brain EV proteome contained numerous proteins implicated in ALS, and EVs from SOD1 G93A mice were significantly depleted in myelin-oligodendrocyte glycoprotein compared with those from NTg animals. We observed that brain- and spinal cord–derived EVs, from NTg and SOD1 G93A mice, are positive for the astrocyte marker GLAST and the synaptic marker SNAP25, whereas CD11b, a microglial marker, was largely absent. EVs from brains and spinal cords of the SOD1 G93A ALS mouse model, as well as from human SOD1 familial ALS patient spinal cord, contained abundant misfolded and nonnative disulfide-cross-linked aggregated SOD1. Our results indicate that CNS-derived EVs from an ALS animal model contain pathogenic disease-causing proteins and suggest that brain astrocytes and neurons, but not microglia, are the main EV source.

INSTRUMENT(S): Bruker Daltonics instrument model

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Brain

DISEASE(S): Amyotrophic Lateral Sclerosis

SUBMITTER: Jenny Moon  

LAB HEAD: Neil R. Cashman

PROVIDER: PXD021396 | Pride | 2020-09-11

REPOSITORIES: Pride

Dataset's files

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Max-Pellet1_A9_01_6927.d.zip Other
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Publications

CNS-derived extracellular vesicles from superoxide dismutase 1 (SOD1)<sup>G93A</sup> ALS mice originate from astrocytes and neurons and carry misfolded SOD1.

Silverman Judith M JM   Christy Darren D   Shyu Chih Cheih CC   Moon Kyung-Mee KM   Fernando Sarah S   Gidden Zoe Z   Cowan Catherine M CM   Ban Yuxin Y   Stacey R Greg RG   Grad Leslie I LI   McAlary Luke L   Mackenzie Ian R IR   Foster Leonard J LJ   Cashman Neil R NR  

The Journal of biological chemistry 20190111 10


Extracellular vesicles (EVs) are secreted by myriad cells in culture and also by unicellular organisms, and their identification in mammalian fluids suggests that EV release also occurs at the organism level. However, although it is clearly important to better understand EVs' roles in organismal biology, EVs in solid tissues have received little attention. Here, we modified a protocol for EV isolation from primary neural cell culture to collect EVs from frozen whole murine and human neural tissu  ...[more]

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