학술논문

Exosomes Derived from Human Primed Mesenchymal Stem Cells Induce Mitosis and Potentiate Growth Factor Secretion
Document Type
article
Source
Stem Cells and Development. 28(6)
Subject
Biochemistry and Cell Biology
Biological Sciences
Stem Cell Research
Regenerative Medicine
Stem Cell Research - Nonembryonic - Non-Human
Biotechnology
Stem Cell Research - Nonembryonic - Human
1.1 Normal biological development and functioning
Underpinning research
Adolescent
Adult
Cell Line
Tumor
Exosomes
Female
Humans
Intercellular Signaling Peptides and Proteins
Male
Mesenchymal Stem Cells
Middle Aged
Mitosis
mesenchymal stem cells
exosomes
proteomics
HiRIEF LC-MS
MS
proliferation
extracellular matrix
HiRIEF LC-MS/MS
Technology
Medical and Health Sciences
Developmental Biology
Immunology
Biological sciences
Language
Abstract
Mesenchymal stem cells (MSCs) facilitate functional recovery in numerous animal models of inflammatory and ischemic tissue-related diseases with a growing body of research suggesting that exosomes mediate many of these therapeutic effects. It remains unclear, however, which types of proteins are packaged into exosomes compared with the cells from which they are derived. In this study, using comprehensive proteomic analysis, we demonstrated that human primed MSCs secrete exosomes (pMEX) that are packaged with markedly higher fractions of specific protein subclasses compared with their cells of origin, indicating regulation of their contents. Notably, we found that pMEX are also packaged with substantially elevated levels of extracellular-associated proteins. Fibronectin was the most abundant protein detected, and data established that fibronectin mediates the mitogenic properties of pMEX. In addition, treatment of SHSY5Y cells with pMEX induced the secretion of growth factors known to possess mitogenic and neurotrophic properties. Taken together, our comprehensive analysis indicates that pMEX are packaged with specific protein subtypes, which may provide a molecular basis for their distinct functional properties.