Oct4 expression revisited:: potential pitfalls for data misinterpretation in stem cell research

被引:141
作者
Liedtke, Stefanie [1 ]
Stephan, Milaid [1 ]
Koegler, Gesine [1 ]
机构
[1] Univ Dusseldorf, Med Ctr, Inst Transplantat Diagnost & Cell Therapeut, D-40225 Dusseldorf, Germany
关键词
adult stem cells; alternative splicing; differentiated cells; pluripotency; stem cell marker;
D O I
10.1515/BC.2008.098
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The octamer-binding transcription factor 4 gene encodes a nuclear protein (Oct4, also known as Pou5F1 and Oct3/4) that belongs to a family of transcription factors containing the POU DNA-binding domain. Expression can be detected in embryonic stem cells as well as in adult stem cells, such as bone marrow-derived mesenchymal stem cells. Expression of Oct4 is downregulated coincident with stem cell differentiation and loss of expression leading to differentiation. A role for maintaining pluripotency and self-renewal of embryonic stem cells is ascribed to Oct4 as a pluripotency marker. Results describing Oct4 expression in differentiated cells, including peripheral blood mononuclear cells (PBMCs), neonatal and adult stem cells, as well as cancer cells, must be interpreted with caution. In several publications, Oct4 has been ascribed a function in maintaining self-renewal of adult stem cells. In contrast, other publications reported Oct4 expression in human tumor cells. Here, we summarize the recent findings on Oct4 expression and present possibilities and reasons why several false positive results on Oct4 expression still occur in the recent literature. Also, simple solutions are provided to avoid these positive signals.
引用
收藏
页码:845 / 850
页数:6
相关论文
共 35 条
  • [21] Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells
    Niwa, H
    Miyazaki, J
    Smith, AG
    [J]. NATURE GENETICS, 2000, 24 (04) : 372 - 376
  • [22] Multiple retropseudogenes from pluripotent cell-specific gene expression indicates a potential signature for novel gene identification
    Pain, D
    Chirn, GW
    Strassel, C
    Kemp, DM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (08) : 6265 - 6268
  • [23] Expression of the PDGF α-receptor 1.5 kb transcript, OCT-4, and c-KIT in human normal and malignant tissues.: Implications for the early diagnosis of testicular germ cell tumours for our understanding of regulatory mechanisms
    Palumbo, C
    van Roozendaal, K
    Gillis, AJ
    van Gurp, RH
    de Munnik, H
    Oosterhuis, JW
    van Zoelen, EJ
    Looijenga, LH
    [J]. JOURNAL OF PATHOLOGY, 2002, 196 (04) : 467 - 477
  • [24] Oct-4:: Gatekeeper in the beginnings of mammalian development
    Pesce, M
    Schöler, HR
    [J]. STEM CELLS, 2001, 19 (04) : 271 - 278
  • [25] Oct-4, Rex-1, and Gata-4 expression in human MSC increase the differentiation efficiency but not hTERT expression
    Roche, Stephane
    Richard, Marie-Jeanne
    Favrot, Marie-Christine
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 2007, 101 (02) : 271 - 280
  • [26] CD14+CD34low cells with stem cell phenotypic and functional features are the major source of circulating endothelial progenitors
    Romagnani, P
    Annunziato, F
    Liotta, F
    Lazzeri, E
    Mazzinghi, B
    Frosali, F
    Cosmi, L
    Maggi, L
    Lasagni, L
    Scheffold, A
    Kruger, M
    Dimmeler, S
    Marra, F
    Gensini, G
    Maggi, E
    Romagnani, S
    [J]. CIRCULATION RESEARCH, 2005, 97 (04) : 314 - 322
  • [27] REGULATION OF TRANSCRIPTION AND CELL IDENTITY BY POU DOMAIN PROTEINS
    RUVKUN, G
    FINNEY, M
    [J]. CELL, 1991, 64 (03) : 475 - 478
  • [28] POU domain family values: Flexibility, partnerships, and developmental codes
    Ryan, AK
    Rosenfeld, MG
    [J]. GENES & DEVELOPMENT, 1997, 11 (10) : 1207 - 1225
  • [29] NEW TYPE OF POU DOMAIN IN GERM LINE-SPECIFIC PROTEIN OCT-4
    SCHOLER, HR
    RUPPERT, S
    SUZUKI, N
    CHOWDHURY, K
    GRUSS, P
    [J]. NATURE, 1990, 344 (6265) : 435 - 439
  • [30] Oct4 pseudogenes are transcribed in cancers
    Suo, GL
    Han, J
    Wang, X
    Zhang, JY
    Zhao, YN
    Zhao, YH
    Dai, JW
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 337 (04) : 1047 - 1051