Manigrasso Michaele B, O'Connor J Patrick
Department of Biochemistry and Molecular Biology, UMDNJ-New Jersey Medical School and Graduate School of Biomedical Sciences, 185 South Orange Avenue, Newark, NJ 07103, USA.
Calcif Tissue Int. 2008 Jun;82(6):465-74. doi: 10.1007/s00223-008-9144-3.
Quantitative trait locus analysis can be used to identify genes critically involved in biological processes. No such analysis has been applied to identifying genes that control bone fracture healing. To determine the feasibility of such an approach, healing of femur fractures was measured between C57BL/6, DBA/2, and C3H inbred strains of mice. Healing was assessed by radiography and histology and measured by histomorphometry and biomechanical testing. In all strains, radiographic bridging of the fracture was apparent after 3 weeks of healing. Histology showed that healing occurred through endochondral ossification in all strains. Histomorphometric measurements found more bone in the C57BL/6 fracture calluses 7 and 10 days after fracture. In contrast, more cartilage was present after 7 days in the C3H callus, which rapidly declined to levels less than those of C57BL/6 or DBA/2 mice by 14 days after fracture. An endochondral ossification index was calculated by multiplying the callus percent cartilage and bone areas as a measure of endochondral ossification. At 7 and 10 days after fracture, this value was higher in C57BL/6 mice. Using torsional mechanical testing, normalized structural and material properties of the C57BL/6 healing femurs were higher than values from the DBA/2 or C3H mice 4 weeks after fracture. The data indicate that fracture healing proceeds more rapidly in C57BL/6 mice and demonstrate that genetic variability significantly contributes to the process of bone regeneration. Large enough differences exist between C57BL/6 and DBA/2 or C3H mice to permit a quantitative trait locus analysis to identify genes controlling bone regeneration.
数量性状基因座分析可用于识别在生物过程中起关键作用的基因。尚未有此类分析应用于识别控制骨折愈合的基因。为了确定这种方法的可行性,在C57BL/6、DBA/2和C3H近交系小鼠中测量了股骨骨折的愈合情况。通过X线摄影和组织学评估愈合情况,并通过组织形态计量学和生物力学测试进行测量。在所有品系中,骨折愈合3周后X线片上可见骨折处骨桥形成。组织学显示所有品系均通过软骨内成骨实现愈合。组织形态计量学测量发现,骨折后7天和10天时,C57BL/6骨折痂中的骨量更多。相比之下,C3H骨折痂在7天时软骨更多,但在骨折后14天时迅速降至低于C57BL/6或DBA/2小鼠的水平。通过将痂软骨百分比和骨面积相乘计算软骨内成骨指数,作为软骨内成骨的一个指标。在骨折后7天和10天时,C57BL/6小鼠的该值更高。使用扭转力学测试,C57BL/6愈合股骨的标准化结构和材料特性在骨折后4周高于DBA/2或C3H小鼠的值。数据表明C57BL/6小鼠的骨折愈合更快,并证明遗传变异性对骨再生过程有显著贡献。C57BL/6与DBA/2或C3H小鼠之间存在足够大的差异,足以进行数量性状基因座分析以识别控制骨再生的基因。