Madeline C. Cramer , William A. D'Angelo , Marley J. Dewey , Allison M. Manuel , Steven J. Mullett , Stacy G. Wendell , Dobrawa Napierala , Peng Jiang , Stephen F. Badylak
{"title":"存在于骨骼、血液和细胞外基质中的细胞外小泡具有独特的特征和生物学作用","authors":"Madeline C. Cramer , William A. D'Angelo , Marley J. Dewey , Allison M. Manuel , Steven J. Mullett , Stacy G. Wendell , Dobrawa Napierala , Peng Jiang , Stephen F. Badylak","doi":"10.1016/j.regen.2022.100066","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>Extracellular vesicles (EV) have long been recognized as an important means of cell to cell communication, but current metrics to delineate various subpopulations of EV are limited. Recently, a distinctive subpopulation of EV embedded within the extracellular matrix of soft tissues, termed matrix-bound nanovesicles (MBV), has been described. Although the lipid membrane composition and intravesicular cargo of MBV clearly differ from liquid phase EV (i.e. exosomes), a more comprehensive characterization of the physical and biologic properties of MBV vs. exosomes and those of a separate subpopulation of EV, specifically bone matrix vesicles, would contribute to our understanding of the biogenesis and physiologic role of these three EV subpopulations.</p></div><div><h3>Results</h3><p>The physical characteristics, protein and miRNA cargo profiling, vesicle membrane lipidomics, and immunomodulatory activity were used to compare skeletal muscle-derived MBV, liquid phase plasma exosomes, and mineralization-competent matrix vesicles of provisional bone matrix. We show that despite similar physical characteristics, these three preparations of EV represent distinct entities with different biologic activity.</p></div><div><h3>Conclusion</h3><p>These results inform metrics for the categorization of EV and provide tools for the isolation of EV for potential diagnostic and therapeutic applications.</p></div>","PeriodicalId":94333,"journal":{"name":"Journal of immunology and regenerative medicine","volume":"18 ","pages":"Article 100066"},"PeriodicalIF":0.0000,"publicationDate":"2022-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2468498822000087/pdfft?md5=5428d500883dc7f68f8347445f9bec5d&pid=1-s2.0-S2468498822000087-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Extracellular vesicles present in bone, blood and extracellular matrix have distinctive characteristics and biologic roles\",\"authors\":\"Madeline C. Cramer , William A. D'Angelo , Marley J. Dewey , Allison M. Manuel , Steven J. Mullett , Stacy G. Wendell , Dobrawa Napierala , Peng Jiang , Stephen F. Badylak\",\"doi\":\"10.1016/j.regen.2022.100066\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><p>Extracellular vesicles (EV) have long been recognized as an important means of cell to cell communication, but current metrics to delineate various subpopulations of EV are limited. Recently, a distinctive subpopulation of EV embedded within the extracellular matrix of soft tissues, termed matrix-bound nanovesicles (MBV), has been described. Although the lipid membrane composition and intravesicular cargo of MBV clearly differ from liquid phase EV (i.e. exosomes), a more comprehensive characterization of the physical and biologic properties of MBV vs. exosomes and those of a separate subpopulation of EV, specifically bone matrix vesicles, would contribute to our understanding of the biogenesis and physiologic role of these three EV subpopulations.</p></div><div><h3>Results</h3><p>The physical characteristics, protein and miRNA cargo profiling, vesicle membrane lipidomics, and immunomodulatory activity were used to compare skeletal muscle-derived MBV, liquid phase plasma exosomes, and mineralization-competent matrix vesicles of provisional bone matrix. We show that despite similar physical characteristics, these three preparations of EV represent distinct entities with different biologic activity.</p></div><div><h3>Conclusion</h3><p>These results inform metrics for the categorization of EV and provide tools for the isolation of EV for potential diagnostic and therapeutic applications.</p></div>\",\"PeriodicalId\":94333,\"journal\":{\"name\":\"Journal of immunology and regenerative medicine\",\"volume\":\"18 \",\"pages\":\"Article 100066\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2468498822000087/pdfft?md5=5428d500883dc7f68f8347445f9bec5d&pid=1-s2.0-S2468498822000087-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of immunology and regenerative medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2468498822000087\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of immunology and regenerative medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468498822000087","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Extracellular vesicles present in bone, blood and extracellular matrix have distinctive characteristics and biologic roles
Introduction
Extracellular vesicles (EV) have long been recognized as an important means of cell to cell communication, but current metrics to delineate various subpopulations of EV are limited. Recently, a distinctive subpopulation of EV embedded within the extracellular matrix of soft tissues, termed matrix-bound nanovesicles (MBV), has been described. Although the lipid membrane composition and intravesicular cargo of MBV clearly differ from liquid phase EV (i.e. exosomes), a more comprehensive characterization of the physical and biologic properties of MBV vs. exosomes and those of a separate subpopulation of EV, specifically bone matrix vesicles, would contribute to our understanding of the biogenesis and physiologic role of these three EV subpopulations.
Results
The physical characteristics, protein and miRNA cargo profiling, vesicle membrane lipidomics, and immunomodulatory activity were used to compare skeletal muscle-derived MBV, liquid phase plasma exosomes, and mineralization-competent matrix vesicles of provisional bone matrix. We show that despite similar physical characteristics, these three preparations of EV represent distinct entities with different biologic activity.
Conclusion
These results inform metrics for the categorization of EV and provide tools for the isolation of EV for potential diagnostic and therapeutic applications.