Rabie A Bakr M, Tang Guo Hua, Hägg Urban
Hard Tissue Biology and Repair Research Group and Orthodontics, Faculty of Dentistry, Prince Philip Dental Hospital, The University of Hong Kong, 34 Hospital Road, Hong Kong SAR, China.
Arch Oral Biol. 2004 Feb;49(2):109-18. doi: 10.1016/j.archoralbio.2003.09.006.
Core binding factor a1 (Cbfa1) is a crucial transcription factor for osteoblasts differentiation and chondrocytes maturation in embryonic skeletal genesis, but little is known about its function in mandibular condylar growth. The aim of this study was to determine the temporal and spatial pattern of Cbfa1 expression in condylar cartilage during natural growth. Mandibular condyles were harvested from 50 female Sprague-Dawley rats at age of 38, 42, 49, 56 and 65 days. Alcian blue and PAS staining was used for histological analysis. Type A antibody raised against Cbfa1 isoform II was observed in the pre-hypertrophic and hypertrophic chondrocytes in condylar cartilage, and in the mature osteocytes in trabecular bone. Type B antibody raised against 17 aa sequence present after the Runt domain was detected in tartrate resistant acid phosphatase (TRAP) positive osteoclasts in the erosive front of cartilage, and also in the osteoblasts on the sub-chondral bone surface. In situ hybridisation was carried out with a probe containing a fragment in exon 8 of the cDNA. Cbfa1 transcripts were localised in the osteoblasts and chondrocytes, but not in osteoclasts. Quantitative analysis demonstrated that both types of Cbfa1 proteins reached their maximum level on day 56, which coincided with the terminal maturation of hypertrophic chondrocytes and the aggregation of mineralisation deposits in extracellular matrix. These results suggest that Cbfa1 is a master gene controlling the functions of all the skeletal cell lineages by synthesising different functional isoforms. Furthermore, Cbfa1 couples the process of chondrocytes maturation, extracellular matrix mineralisation and degradation, as well as osteoblasts invasion during endochondral bone formation. Beyond its function on embryonic development, Cbfa1 regulates the postnatal growth of mandibular condyle.
核心结合因子a1(Cbfa1)是胚胎骨骼发育过程中骨细胞分化和软骨细胞成熟的关键转录因子,但对其在下颌髁突生长中的功能了解甚少。本研究的目的是确定自然生长过程中髁突软骨中Cbfa1表达的时空模式。从50只38、42、49、56和65日龄的雌性Sprague-Dawley大鼠中采集下颌髁突。采用阿尔辛蓝和PAS染色进行组织学分析。在髁突软骨的前肥大和肥大软骨细胞以及小梁骨的成熟骨细胞中观察到针对Cbfa1同工型II产生的A型抗体。在软骨侵蚀前沿的抗酒石酸酸性磷酸酶(TRAP)阳性破骨细胞以及软骨下骨表面的成骨细胞中检测到针对Runt结构域后出现的17个氨基酸序列产生的B型抗体。用包含cDNA外显子8片段的探针进行原位杂交。Cbfa1转录本定位于成骨细胞和软骨细胞,但不在破骨细胞中。定量分析表明,两种类型的Cbfa1蛋白在第56天达到最高水平,这与肥大软骨细胞的终末成熟以及细胞外基质中矿化沉积物的聚集相一致。这些结果表明,Cbfa1是通过合成不同功能同工型来控制所有骨骼细胞谱系功能的主控基因。此外,Cbfa1在软骨内骨形成过程中耦合软骨细胞成熟、细胞外基质矿化和降解以及成骨细胞侵入的过程。除了其在胚胎发育中的功能外,Cbfa1还调节下颌髁突的出生后生长。