| Project/Area Number |
14571008
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Hematology
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| Research Institution | International Medical Center of Japan (Research Institute) |
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Principal Investigator |
SAEKI Kumiko Research Institute International Medical Center of Japan, Division of Hematopoietic Disorder, Department of Hematology, Division Chief, 血液疾患研究部・造血障害研究室, 室長 (80322717)
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| Project Period (FY) |
2002 – 2003
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| Project Status |
Completed (Fiscal Year 2003)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2003: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 2002: ¥2,200,000 (Direct Cost: ¥2,200,000)
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| Keywords | CREB / retinoic acid / PU.1 / cell adhesion / CD11b / respiratory burst / morphological maturation / cell growth / CRE / 細胞形態 / ラミン / ラミン受容体 / Cyclyn D3 / 蛋白メッセージ発現解離 / p67^<phox> |
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| Research Abstract |
We evaluated the involvement of cAMP-response element (CRE)-dependent transcriptions in all-trans retinoic acid (ATRA)-induced myeloid differentiation using human monoblastic U937 cells. ATRA treatment caused an increment in CRE-dependent transcription activity and induced a wide variety of differentiation phenotypes including the functional and morphological maturation. Indeed, ATRA treatment induced an expression of CCAAT/enhancer-binding protein β (C/EBPβ), a CRE-dependent transcription factor important for monocytic differentiation, and the inhibition of CRE enhancer activity by the expression of a dominant negative cAMP-response element-binding protein (dominant negative CREB, dn-CREB) abolished the induction of C/EBPβ. Functional maturation such as an enhancement in cell adhesion and respiratory burst activity were dramatically suppressed by the expression of dn-CREB. In accordance with these, the differentiation-dependent induction of adhesion molecule (CD11b), the phagocyte oxidase for the respiratory burst and the transcription factor PU.1 responsible for the phagocyte oxidase induction was all eradicated by dn-CREB. Quite surprisingly, morphological maturation including nuclear convolution and cytoplasmic vacuolar formation were augmented by dn-CREB. Under the same condition, the differentiation-associated cell growth arrest was not affected by the expression of dn-CREB. Our results clearly indicate that CRE-driven transcription plays at least three distinct roles during the single process of myeloid differentiation : it stimulates functional maturation but suppresses morphological maturation while giving no effects on cell growth arrest.
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