Liu J, Hu Y, Ma Z
Institute of Orthopaedics of People's Liberation Army, Fourth Military Medical University Xi'an.
Zhonghua Wai Ke Za Zhi. 1996 Oct;34(10):585-8.
The role of BMP3 in fracture repair and its basic mechanisms at the molecular aspect has been studied. Fourty-eight New Zealand white rabbits with the fractures in the middle of bilateral radial shafts were used as animal models, and divided randomly into six groups for calluses at the 1st, 2nd, 3rd, 4th, 6th and 8th week after the onset of fracture. The levels and the cellular localizations of expression of BMP3 mRNA were investigated with the nucleotide hybridization techniques. The results revealed that BMP3 gene expression was highly increased in the early phase of fracture repair, and reached its peak at the second week (about 3.4-fold of that of the normal control). The strong expression of BMP3 gene was localized in mesenchymal cells, chondroblasts and osteoblasts. The results suggest that BMP3 plays an important role of bone-induction in the early stage of fracture repair and it works by the way of autocrine or/and paracrine pathway.
BMP3在骨折修复中的作用及其在分子层面的基本机制已得到研究。选取48只双侧桡骨中段骨折的新西兰白兔作为动物模型,随机分为6组,分别在骨折后第1、2、3、4、6和8周取材观察骨痂情况。采用核酸杂交技术检测BMP3 mRNA的表达水平及细胞定位。结果显示,BMP3基因在骨折修复早期表达显著增加,在第2周达到高峰(约为正常对照的3.4倍)。BMP3基因的强表达定位于间充质细胞、成软骨细胞和成骨细胞。结果表明,BMP3在骨折修复早期发挥重要的骨诱导作用,其作用方式为自分泌或/和旁分泌途径。