Zhao Yongjie, Yin Gang, Du Rui, Wang Limin, Deng Mingming, Guan Guofeng, Sun Guangchao, Liu Ying
Department of Foot and Ankle Surgery, Binzhou Medical University Hospital, Binzhou Shandong, 256603, P. R. China.
Beijing Weidafeng Medical Biomaterials Co., Ltd, Beijing, 102200, P. R. China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2023 Aug 15;37(8):945-951. doi: 10.7507/1002-1892.202303132.
To measure the concentration of bone morphogenetic protein 2 (BMP-2) in demineralized bone matrix (DBM) prepared from different long bones and to evaluate the osteoinductivity of different DBM on MC3T3-E1 cells.
Different bones from the same cadaver donor were used as the initial materials for making DBM, which were divided into ulna group (uDBM), humerus group (hDBM), tibia group (tDBM), and femur group (fDBM) according to the origins, and boiled DBM (cDBM) was taken as the control group. The proteins of DBM were extracted by guanidine hydrochloride, and the concentrations of BMP-2 were determined by ELISA assay. Then the DBM were co-cultured with MC3T3-E1 cells, the proliferation of MC3T3-E1 cells was observed by cell counting kit 8 (CCK-8) assay. The osteogenic differentiation ability of MC3T3-E1 cells was qualitatively observed by alizarin red, alkaline phosphatase (ALP), and Van Gieson staining, and the osteogenic differentiation ability of MC3T3-E1 cells was quantitatively analyzed by ALP content. Linear regression was used to analyze the effect of BMP-2 concentration in DBM on ALP synthesis.
There were significant differences in the concentration of BMP-2 among the DBM groups (<0.05). The concentrations of BMP-2 in the lower limb long bone were higher than those in the upper limb long bone, and the concentration of BMP-2 in the fDBM group was about 35.5 times that in the uDBM group. CCK-8 assay showed that the cells in each group continued to proliferate within 5 days of co-culture, and the absorbance () values at different time points were in the order of cDBM group<uDBM group<hDBM group<tDBM group<fDBM group. After co-culture for 14 days, the expressions of ALP, calcified nodules, and collagen fibers in each group were consistent with the distribution of BMP-2 concentration in DBM. The order of ALP content from low to high was cDBM group<uDBM group<hDBM group<tDBM group<fDBM group, and the differences between the groups were significant (<0.05). Linear regression analysis showed that =0.361+0.017, the effect of BMP-2 concentration in DBM on cellular ALP content was significant (=3.552, =0.005); for every 1 ng/g increase in BMP-2 concentration, ALP content would increase by 0.017 [95% (0.006, 0.027)] U/100 mL.
The concentration of natural BMP-2 in different long bones varies greatly, and the lower limb long bone is higher than the upper limb long bone. The harvested location of bone material was an important factor affecting the osteoinductivity of DBM.
测定不同长骨制备的脱矿骨基质(DBM)中骨形态发生蛋白2(BMP - 2)的浓度,并评估不同DBM对MC3T3 - E1细胞的成骨诱导活性。
选取同一尸体供体的不同骨骼作为制备DBM的初始材料,根据来源分为尺骨组(uDBM)、肱骨组(hDBM)、胫骨组(tDBM)和股骨组(fDBM),并以煮沸的DBM(cDBM)作为对照组。采用盐酸胍提取DBM中的蛋白质,通过酶联免疫吸附测定(ELISA)法测定BMP - 2的浓度。然后将DBM与MC3T3 - E1细胞共培养,采用细胞计数试剂盒8(CCK - 8)法观察MC3T3 - E1细胞的增殖情况。通过茜素红、碱性磷酸酶(ALP)和Van Gieson染色定性观察MC3T3 - E1细胞的成骨分化能力,并通过ALP含量定量分析MC3T3 - E1细胞的成骨分化能力。采用线性回归分析DBM中BMP - 2浓度对ALP合成的影响。
各DBM组间BMP - 2浓度差异有统计学意义(<0.05)。下肢长骨中BMP - 2的浓度高于上肢长骨,fDBM组中BMP - 2的浓度约为uDBM组的35.5倍。CCK - 8法检测结果显示,共培养5天内各组细胞均持续增殖,不同时间点的吸光度()值顺序为cDBM组<uDBM组<hDBM组<tDBM组<fDBM组。共培养14天后,各组中ALP、钙化结节和胶原纤维的表达与DBM中BMP - 2浓度分布一致。ALP含量由低到高的顺序为cDBM组<uDBM组<hDBM组<tDBM组<fDBM组,组间差异有统计学意义(<0.05)。线性回归分析显示=0.361 + 0.017,DBM中BMP - 2浓度对细胞ALP含量的影响有统计学意义(=3.552,=0.005);BMP - 2浓度每增加1 ng/g,ALP含量将增加0.017 [95%(0.006,0.027)] U/100 mL。
不同长骨中天然BMP - 2的浓度差异较大,下肢长骨高于上肢长骨。骨材料的采集部位是影响DBM成骨诱导活性的重要因素。