Publication Type:

Journal Article

Source:

Proteomics, Volume 11, Number 20, p.4007-4020 (2011)

URL:

http://www.scopus.com/inward/record.url?eid=2-s2.0-80053983347&partnerID=40&md5=bde25b677c34900517bd0c2cefd1fad5

Keywords:

Animals, apolipoprotein E, article, bone morphogenetic protein, cell differentiation, Cell Lineage, cell maturation, embryonic stem cell, Embryonic Stem Cells, fatty acid binding protein 4, Gas Chromatography-Mass Spectrometry, glia cell, human, human cell, Humans, immunohistochemistry, liquid chromatography, Mice, Mouse mammary tumor virus, myelination, nerve cell adhesion molecule, neural stem cell, oligodendroglia, priority journal, protein database, protein expression, proteomics, stem cell, Stem cells, tandem mass spectrometry, tenascin, time, Transferrin, upregulation

Abstract:

Oligodendrocytes (OLs) are glial cells of the central nervous system, which produce myelin. Cultured OLs provide immense therapeutic opportunities for treating a variety of neurological conditions. One of the most promising sources for such therapies is human embryonic stem cells (ESCs) as well as providing a model to study human OL development. For these purposes, an investigation of proteome level changes is critical for understanding the process of OL differentiation. In this report, an iTRAQ-based quantitative proteomic approach was used to study multiple steps during OL differentiation including neural progenitor cells, glial progenitor cells and oligodendrocyte progenitor cells (OPCs) compared to undifferentiated ESCs. Using a 1% false discovery rate cutoff,  3145 proteins were quantitated and several demonstrated progressive stage-specific expression. Proteins such as transferrin, neural cell adhesion molecule 1, apolipoprotein E and wingless-related MMTV integration site 5A showed increased expression from the neural progenitor cell to the OPC stage. Several proteins that have demonstrated evidence or been suspected in OL maturation were also found upregulated in OPCs including fatty acid-binding protein 4, THBS1, bone morphogenetic protein 1, CRYAB, transferrin, tenascin C, COL3A1, TGFBI and EPB41L3. Thus, by providing the first extensive proteomic profiling of human ESC differentiation into OPCs, this study provides many novel proteins that are potentially involved in OL development. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Notes:

cited By (since 1996)8

Cite this Research Publication

Rab Chaerkady, Letzen, Bc, Renuse, Sab d, Sahasrabuddhe, N. Aab e, Kumar, Pb, All, A. Hf, Thakor, N. Vf, Delanghe, Bg, Gearhart, J. Dh, Pandey, Aai, and Kerr, C. Lc, “Quantitative temporal proteomic analysis of human embryonic stem cell differentiation into oligodendrocyte progenitor cells”, Proteomics, vol. 11, pp. 4007-4020, 2011.