Identification and characterization of hADSC‐derived exosome proteins from different isolation methods

• Published in: Journal of cellular and molecular medicine 2021-08, Vol.25 (15), p.7436-7450
• Main Authors: Huang, Lien‐Hung, Rau, Cheng‐Shyuan, Wu, Shao‐Chun, Wu, Yi‐Chan, Wu, Chia‐Jung, Tsai, Chia‐Wen, Lin, Chia‐Wei, Lu, Tsu‐Hsiang, Hsieh, Ching‐Hua
• Format: Article
• Language: English
• Subjects: Adipocytes - chemistry; and iTRAQ; Apoptosis; Cameras; Cardiac function; Cell culture; Cell differentiation; Cell Fractionation - methods; Cell proliferation; Cells, Cultured; ExoQuick‐TC; ExoQuick‐TC ULTRA; Exosomes; Exosomes - chemistry; Exosomes - metabolism; hADSC; Human Umbilical Vein Endothelial Cells - chemistry; Human Umbilical Vein Endothelial Cells - metabolism; Humans; Labeling; Lipopolysaccharides; Mesenchymal Stem Cells - chemistry; Mesenchymal Stem Cells - metabolism; Mesenchyme; Metabolic Networks and Pathways; Original; Paracrine signalling; Peptides; Polymers; Protein composition; Proteins; Proteome - chemistry; Proteomics - methods; Signal transduction; size exclusion chromatography; Stem cells; Ultracentrifugation; Ultrafiltration
• ISSN: 1582-1838; 1582-4934
• DOI: 10.1111/jcmm.16775

Exosomes are secreted into the extracellular space by most cell types and contain various molecular constituents, which play roles in many biological processes. Adipose‐derived mesenchymal stem cells (ADSCs) can differentiate into a variety of cell types and secrete a series of paracrine factors through exosomes. ADSC‐derived exosomes have shown diagnostic and therapeutic potential in many clinical diseases. The molecular components are critical for their mechanisms. Several methods have been developed for exosome purification, including ultracentrifugation, ultrafiltration, density gradient purification, size‐based isolation, polymer precipitation and immuno‐affinity purification. Thus, we employed four methods to isolate exosomes from the hADSC culture medium, including ultracentrifugation, size exclusion chromatography, ExoQuick‐TC precipitation and ExoQuick‐TC ULTRA isolation. Following exosome isolation, we performed quantitative proteomic analysis of the exosome proteins using isobaric tags for relative and absolute quantification (iTRAQ) labelling, combined with 2D‐LC‐MS/MS. There were 599 universal and 138 stably expressed proteins in hADSC‐derived exosomes. We proved that these proteins were potential hADSC‐derived exosomes markers, including CD109, CD166, HSPA4, TRAP1, RAB2A, RAB11B and RAB14. From the quantitative proteomic analysis, we demonstrated that hADSC‐derived exosome protein expression varied, with lipopolysaccharide (LPS) treatment, in the different isolation methods. Pathway analysis and proliferation, migration and endothelial tube formation assays showed varying effects in cells stimulated with hADSC‐derived exosomes from different isolation methods. Our study revealed that different isolation methods might introduce variations in the protein composition in exosomes, which reflects their effects on biological function. The pros and cons of these methods are important points to consider for downstream research applications.