Molecular MedicineNeurosciencePeer-reviewed journal article
Extracellular vesicles from microglial cells activated by abnormal heparan sulfate oligosaccharides from Sanfilippo patients impair neuronal dendritic arborization
Chloé DiasiD, Nissrine BalloutiD, Guillaume MorlaiD, Katia AlilecheiD, Christophe SantiagoiD, Ida Chiara GuerreraiD, Adeline ChaubetiD, Jérôme AusseiliD, Stéphanie TrudeliD
Abstract
BackgroundIn mucopolysaccharidosis type III (MPS III), a pediatric neurodegenerative disorder, accumulation of abnormal glycosaminoglycans (GAGs) induces severe neuroinflammation by triggering the microglial pro-inflammatory cytokines production via a TLR4-dependent pathway. But the extent of the microglia contribution to the MPS III neuropathology remains unclear. Extracellular vesicles (EVs) mediate intercellular communication and are known to participate in the pathogenesis of adult neurodegenerative diseases. However, characterization of the molecular profiles of EVs released by MPS III microglia and their effects on neuronal functions have not been described. MethodsHere, we isolated EVs secreted by the microglial cells after treatment with GAGs purified from urines of MPS III patients (MPS III-EVs) to explore the EVs proteins and small RNA profiles using LC-MS/MS and RNA sequencing. We next performed a functional assay by immunofluorescence following wild-type (WT) or MPS III-EVs uptake by WT primary cortical neurons and analyzed their extensions metrics after staining of {beta}III-tubulin and MAP2 by confocal microscopy. ResultsFunctional enrichment analysis for both proteomics and RNA sequencing data from MPS III-EVs revealed a specific content involved in neuroinflammation and neurodevelopment pathways. Treatment of cortical neurons with MPS III-EVs induced a disease-associated phenotype demonstrated by a lower total neurite surface area, an impaired somatodendritic compartment, and a higher number of immature dendritic spines. ConclusionsThis study shows, for the first time, that GAGs from patients with MPS III can induce microglial secretion of EVs that deliver a specific molecular message to recipient naive neurons, while promoting the neuroinflammation, and depriving neurons of neurodevelopmental factors. This work provides a framework for further studies of biomarkers to evaluate efficiency of emerging therapies. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=117 SRC="FIGDIR/small/595318v2_ufig1.gif" ALT="Figure 1"> View larger version (28K): org.highwire.dtl.DTLVardef@8dfd3org.highwire.dtl.DTLVardef@9ece15org.highwire.dtl.DTLVardef@1ebc91eorg.highwire.dtl.DTLVardef@e10b00_HPS_FORMAT_FIGEXP M_FIG C_FIG
- organism: human
- assay: proteomics
- assay: bulk RNA-seq
- research focus: cell-cell communication
- approach: statistical model
- Citations
- 3
- FWCI
- 0.85
- Field percentile
- top 27%
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