Abstract
A number of transcription factors (TFs) have been reported that play crucial roles in hematopoiesis. However, only little is known about how these factors are involved in the mechanisms of hematopoietic development and lineage commitment. To investigate the roles of TFs in human B-cell precursors (BCPs), the present study analyzed the expression of the following 16 hematopoietic TFs: AML1, C/EBPα, C/EBPβ, C/EBPγ, C/EBPε, E2A, Ets-1, GATA-1, GATA-2, GATA-3, Ikaros, IRF-1, Pax5, PU.1, T-bet and TCF-1 in 30 human BCP-leukemia cell lines. All BCP-leukemia cell lines were found to be positive for the expression of AML1, C/EBPγ, E2A, Ets-1, IRF-1, Pax5 and PU.1 at the mRNA level. The mRNA expression of C/EBPα, C/EBPβ, C/EBPε, GATA-2, Ikaros, T-bet and TCF-1 was detected in 2 to 29 of the cell lines. Eight BCP-cell lines showed positivity for the dominant negative Ikaros isoform Ik6, while others were positive for expression of Ik1, 2, 3 and 4. GATA-1 and GATA-3 were universally negative. The expression of C/EBPα, PU.1 and T-bet was positive at the protein level in five, 29 and four out of 30 BCP-cell lines, respectively. Cell lines were stimulated with interleukin (IL)-7 and/or interferon (IFN)-γ to investigate the regulation of TF expression. T-bet was clearly induced in the two cell lines NALM-19 and NALM-29 after stimulation. C/EBPβ and IRF-1 were up-regulated in both cell lines and TCF-1 was down-regulated in NALM-19. No significant changes were observed for the other 12 TFs. The present report could provide useful information in the study of the role of TFs on normal and malignant human BCPs.
| Original language | English |
|---|---|
| Pages (from-to) | 841-848 |
| Number of pages | 8 |
| Journal | Leukemia Research |
| Volume | 29 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - Jul 2005 |
Fingerprint
Keywords
- B-cell precursor-leukemia
- Cell line
- Interferon-γ
- Interleukin-7
- Transcription factor
ASJC Scopus subject areas
- Cancer Research
- Hematology
- Oncology
Cite this
Transcription factor expression in B-cell precursor-leukemia cell lines : Preferential expression of T-bet. / Harashima, Akira; Matsuo, Yoshinobu; Drexler, Hans G.; Okochi, Ayumi; Motoda, Ryuichi; Tanimoto, Mitsune; Orita, Kunzo.
In: Leukemia Research, Vol. 29, No. 7, 07.2005, p. 841-848.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Transcription factor expression in B-cell precursor-leukemia cell lines
T2 - Preferential expression of T-bet
AU - Harashima, Akira
AU - Matsuo, Yoshinobu
AU - Drexler, Hans G.
AU - Okochi, Ayumi
AU - Motoda, Ryuichi
AU - Tanimoto, Mitsune
AU - Orita, Kunzo
PY - 2005/7
Y1 - 2005/7
N2 - A number of transcription factors (TFs) have been reported that play crucial roles in hematopoiesis. However, only little is known about how these factors are involved in the mechanisms of hematopoietic development and lineage commitment. To investigate the roles of TFs in human B-cell precursors (BCPs), the present study analyzed the expression of the following 16 hematopoietic TFs: AML1, C/EBPα, C/EBPβ, C/EBPγ, C/EBPε, E2A, Ets-1, GATA-1, GATA-2, GATA-3, Ikaros, IRF-1, Pax5, PU.1, T-bet and TCF-1 in 30 human BCP-leukemia cell lines. All BCP-leukemia cell lines were found to be positive for the expression of AML1, C/EBPγ, E2A, Ets-1, IRF-1, Pax5 and PU.1 at the mRNA level. The mRNA expression of C/EBPα, C/EBPβ, C/EBPε, GATA-2, Ikaros, T-bet and TCF-1 was detected in 2 to 29 of the cell lines. Eight BCP-cell lines showed positivity for the dominant negative Ikaros isoform Ik6, while others were positive for expression of Ik1, 2, 3 and 4. GATA-1 and GATA-3 were universally negative. The expression of C/EBPα, PU.1 and T-bet was positive at the protein level in five, 29 and four out of 30 BCP-cell lines, respectively. Cell lines were stimulated with interleukin (IL)-7 and/or interferon (IFN)-γ to investigate the regulation of TF expression. T-bet was clearly induced in the two cell lines NALM-19 and NALM-29 after stimulation. C/EBPβ and IRF-1 were up-regulated in both cell lines and TCF-1 was down-regulated in NALM-19. No significant changes were observed for the other 12 TFs. The present report could provide useful information in the study of the role of TFs on normal and malignant human BCPs.
AB - A number of transcription factors (TFs) have been reported that play crucial roles in hematopoiesis. However, only little is known about how these factors are involved in the mechanisms of hematopoietic development and lineage commitment. To investigate the roles of TFs in human B-cell precursors (BCPs), the present study analyzed the expression of the following 16 hematopoietic TFs: AML1, C/EBPα, C/EBPβ, C/EBPγ, C/EBPε, E2A, Ets-1, GATA-1, GATA-2, GATA-3, Ikaros, IRF-1, Pax5, PU.1, T-bet and TCF-1 in 30 human BCP-leukemia cell lines. All BCP-leukemia cell lines were found to be positive for the expression of AML1, C/EBPγ, E2A, Ets-1, IRF-1, Pax5 and PU.1 at the mRNA level. The mRNA expression of C/EBPα, C/EBPβ, C/EBPε, GATA-2, Ikaros, T-bet and TCF-1 was detected in 2 to 29 of the cell lines. Eight BCP-cell lines showed positivity for the dominant negative Ikaros isoform Ik6, while others were positive for expression of Ik1, 2, 3 and 4. GATA-1 and GATA-3 were universally negative. The expression of C/EBPα, PU.1 and T-bet was positive at the protein level in five, 29 and four out of 30 BCP-cell lines, respectively. Cell lines were stimulated with interleukin (IL)-7 and/or interferon (IFN)-γ to investigate the regulation of TF expression. T-bet was clearly induced in the two cell lines NALM-19 and NALM-29 after stimulation. C/EBPβ and IRF-1 were up-regulated in both cell lines and TCF-1 was down-regulated in NALM-19. No significant changes were observed for the other 12 TFs. The present report could provide useful information in the study of the role of TFs on normal and malignant human BCPs.
KW - B-cell precursor-leukemia
KW - Cell line
KW - Interferon-γ
KW - Interleukin-7
KW - Transcription factor
UR - http://www.scopus.com/inward/record.url?scp=20344397664&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=20344397664&partnerID=8YFLogxK
U2 - 10.1016/j.leukres.2004.12.010
DO - 10.1016/j.leukres.2004.12.010
M3 - Article
C2 - 15927679
AN - SCOPUS:20344397664
VL - 29
SP - 841
EP - 848
JO - Leukemia Research
JF - Leukemia Research
SN - 0145-2126
IS - 7
ER -