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Updated: Sep 16, 2026

Isolation of Whole Cell Protein Lysates from Mouse Facial Processes and Cultured Palatal Mesenchyme Cells for Phosphoprotein Analysis
Published on: April 1, 2022
Proteomic Atlas of Notochordal Cell-Derived Extracellular Vesicles Highlights EV-Specific NF-κB Modulation and
Josette C van Maanen1, Chantal Voskamp1, Frank M Riemers1
1Department of Clinical Sciences Faculty of Veterinary Medicine Utrecht University Utrecht the Netherlands.
Abstract:
The notochord is a central signalling hub during embryonic development. After regression of the notochord, notochordal cells (NCs) reside within the developing intervertebral disc. The NC-secretome, including matrix, proteins and extracellular vesicles (NC-EVs), promotes regeneration of degenerate intervertebral discs and cartilage. This study aims to unravel the NC-EV-associated proteome and modulatory role in regenerative processes. NC-EVs were isolated from conditioned medium from porcine NC-rich tissue using differential centrifugation, size exclusion chromatography and density gradient centrifugation. Proteomic analysis of NC-EVs was performed using LC-MS/MS and identified 4042 unique proteins, including EV-associated markers, matrisome proteins and proteins associated with critical nodes in canonical signalling pathways. To test NC-EV bioactivity, functional analysis was performed using SBE, TCF/LEF and NF-κB luciferase reporters. NC-EVs activated SMAD3 and inhibited IL-1β-mediated NF-κB signalling. NC-EV depleted controls showed similar effects, indicating that co-isolated proteins played a major role in modulating signalling. Therefore, NC-EVs were further purified and the GAG-rich biomolecular corona was modified with hyaluronidase. Post-hyaluronidase treatment, SMAD3 activation was enhanced only in methodological controls, while inhibition of IL-1β-mediated NF-κB signalling was NC-EV specific. This study is the first to reveal the NC-EV proteome and illustrates that proteins absorbed on the NC-EVs attribute to EV-mediated functional effects.
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