Abstract
In this study, we investigated the secretome of human oligodendrocytes (F3.Olig2 cells) generated from human neural stem cells by transduction with the gene encoding the Olig2 transcription factor. Using mRNA sequencing and protein cytokine arrays, we identified a number of biologically important secretory proteins whose expression has not been previously reported in oligodendrocytes. We found that F3.Olig2 cells secrete IL-6, PDGF-AA, GRO, GM-CSF, and M-CSF, and showed prominent expression of their corresponding receptors. Co-expression of ligands and receptors suggests that autocrine signaling loops may play important roles in both differentiation and maintenance of oligodendrocytes. We also found that F3.Olig2 cells secrete matrix metalloproteinases and matrix metalloproteinase-associated proteins associated with functional competence of oligodendrocytes. The results of our secretome analysis provide insights into the functional and molecular details of human oligodendrocytes. To the best of our knowledge, this is the first systematic analysis of the secretome of oligodendrocytes.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Basic Helix-Loop-Helix Transcription Factors / genetics
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Basic Helix-Loop-Helix Transcription Factors / metabolism
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Biomarkers
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Cell Differentiation* / genetics
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Cytokines / genetics
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Cytokines / metabolism
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Gene Expression
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Gene Expression Profiling
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Gene Expression Regulation, Developmental
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Humans
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Nerve Tissue Proteins / genetics
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Nerve Tissue Proteins / metabolism
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Neural Stem Cells / cytology*
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Neural Stem Cells / metabolism
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Oligodendrocyte Transcription Factor 2
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Oligodendroglia / cytology*
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Oligodendroglia / metabolism*
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Organ Specificity / genetics
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Proteome*
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Proteomics* / methods
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Receptors, Cell Surface / genetics
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Receptors, Cell Surface / metabolism
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Signal Transduction
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Transduction, Genetic
Substances
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Basic Helix-Loop-Helix Transcription Factors
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Biomarkers
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Cytokines
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Nerve Tissue Proteins
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OLIG2 protein, human
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Oligodendrocyte Transcription Factor 2
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Proteome
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Receptors, Cell Surface
Grants and funding
This research was supported by basic science research program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (NRF-2011-0014717). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.