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成骨细胞分化中的Runt同源结构域蛋白:AML3/CBFA1是骨特异性复合物的主要成分。

Runt homology domain proteins in osteoblast differentiation: AML3/CBFA1 is a major component of a bone-specific complex.

作者信息

Banerjee C, McCabe L R, Choi J Y, Hiebert S W, Stein J L, Stein G S, Lian J B

机构信息

Department of Cell Biology and Cancer Center, University of Massachusetts Medical Center, Worcester 01655, USA.

出版信息

J Cell Biochem. 1997 Jul 1;66(1):1-8. doi: 10.1002/(sici)1097-4644(19970701)66:1<1::aid-jcb1>3.0.co;2-v.

DOI:10.1002/(sici)1097-4644(19970701)66:1<1::aid-jcb1>3.0.co;2-v
PMID:9215522
Abstract

The AML/CBFA family of runt homology domain (rhd) transcription factors regulates expression of mammalian genes of the hematopoietic lineage. AML1, AML2 and AML3 are the three AML genes identified to date which influence myeloid cell growth and differentiation. Recently AML-related proteins were identified in an osteoblast-specific promoter binding complex that functionally modulates bone-restricted transcription of the osteocalcin gene. In the present study we demonstrate that in primary rat osteoblasts AML-3 is the AML family member present in the osteoblast-specific complex. Antibody specific for AML-3 completely supershifts this complex, in contrast to antibodies with specificity for AML-1 or AML-2, AML-3 is present as a single 5.4 kb transcript in bone tissues. To establish the functional involvement of AML factors in osteoblast differentiation, we pursued antisense strategies to alter expression of rhd genes. Treatment of osteoblast cultures with rhd antisense oligonucleotides significantly decreased three parameters which are linked to differentiation of normal diploid osteoblasts: the representation of alkaline phosphatase-positive cells, osteocalcin production, and the formation of mineralized nodules. Our findings indicate that AML-3 is a key transcription factor in bone cells and that the activity of rhd proteins is required for completion of osteoblast differentiation.

摘要

Runt同源结构域(RHD)转录因子的AML/CBFA家族调控造血谱系哺乳动物基因的表达。AML1、AML2和AML3是迄今为止已鉴定的影响髓样细胞生长和分化的三个AML基因。最近,在一个成骨细胞特异性启动子结合复合物中鉴定出了AML相关蛋白,该复合物在功能上调节骨钙素基因的骨限制性转录。在本研究中,我们证明在原代大鼠成骨细胞中,AML-3是存在于成骨细胞特异性复合物中的AML家族成员。与针对AML-1或AML-2的抗体相反,针对AML-3的特异性抗体完全使该复合物发生超迁移。AML-3在骨组织中以单一的5. kb转录本形式存在。为了确定AML因子在成骨细胞分化中的功能作用,我们采用反义策略来改变RHD基因的表达。用RHD反义寡核苷酸处理成骨细胞培养物,显著降低了与正常二倍体成骨细胞分化相关的三个参数:碱性磷酸酶阳性细胞的比例、骨钙素的产生以及矿化结节的形成。我们的研究结果表明,AML-3是骨细胞中的关键转录因子,并且RHD蛋白的活性是成骨细胞分化完成所必需的。

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