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A proteomic analysis during serial subculture and osteogenic differentiation of human mesenchymal stem cell

Authors
 Hyun Jin Sun  ;  Young Yil Bahk  ;  Yon Rak Choi  ;  Jung Hye Shim  ;  Seung Hwan Han  ;  Jin Woo Lee 
Citation
 JOURNAL OF ORTHOPAEDIC RESEARCH, Vol.24(11) : 2059-2071, 2006 
Journal Title
JOURNAL OF ORTHOPAEDIC RESEARCH
ISSN
 0736-0266 
Issue Date
2006
MeSH
Adolescent ; Adult ; Biomarkers/metabolism ; Bone Marrow Cells/cytology ; Bone Marrow Cells/metabolism ; Cell Culture Techniques ; Cell Differentiation ; Cell Proliferation ; Cells, Cultured ; Chaperonin Containing TCP-1 ; Chaperonins ; Chloride Channels/genetics ; Chloride Channels/metabolism ; Down-Regulation ; Female ; Heat-Shock Proteins/genetics ; Heat-Shock Proteins/metabolism ; Histocytochemistry ; Humans ; Male ; Mesenchymal Stem Cells/cytology ; Mesenchymal Stem Cells/metabolism* ; Middle Aged ; Molecular Chaperones/genetics ; Molecular Chaperones/metabolism ; Osteogenesis/physiology* ; Proteome ; Proteomics ; RNA, Messenger/metabolism
Keywords
human mesenchymal stem cells ; subculture ; osteogenic differentiation ; regulatory factors ; proteome analysis
Abstract
Although previous studies have reported the effects of extensive subculturing on proliferation rates and osteogenic potential of human mesenchymal stem cells (hMSCs), the results remain controversial. The aim of our study was to characterize the proliferation and osteogenic potential of hMSCs during serial subculture, and also to identify proteins that are differentially regulated in hMSCs during serial subculture and osteogenic differentiation using proteome analysis. Here we show that the proliferation and osteogenic capacity of hMSCs decrease during serial subculturing. Several proteins were shown to be differentially regulated during serial subculture; among these the expression of T-complex protein 1 α subunit (TCP-1α), a protein known to be associated with cell proliferation, cell cycle, morphological changes, and apoptosis, gradually decreased during serial subculture. Among proteins that were differentially regulated during osteogenic differentiation, chloride intracellular channel 1 (CLIC1) was downregulated only during the early passages eukaryotic translation elongation factor, and acidic ribosomal phosphoprotein P0 was downregulated during the middle passages, while annexin V, LIM, and SH3 domain protein 1 (LASP-1), and 14-3-3 protein gamma (YWHAG) were upregulated during the later passage. These studies suggest that differentially regulated passage-specific proteins may play a role in the decrease of osteogenic differentiation potential under serial subculturing.
Full Text
http://onlinelibrary.wiley.com/doi/10.1002/jor.20273/abstract
DOI
10.1002/jor.20273
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Orthopedic Surgery (정형외과학교실) > 1. Journal Papers
Yonsei Authors
Lee, Jin Woo(이진우) ORCID logo https://orcid.org/0000-0002-0293-9017
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/110490
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