Quantitative and sensitive in vitro assay for osteoinductive activity of dernineralized bone matrix

被引:80
作者
Han, B
Tang, BW
Nimni, ME
机构
[1] Univ So Calif, Keck Sch Med, Tissue Engn Lab, Dept Surg, Los Angeles, CA 90033 USA
[2] Univ So Calif, Keck Sch Med, Tissue Engn Lab, Dept Orthopaed, Los Angeles, CA 90033 USA
[3] Univ So Calif, Keck Sch Med, Tissue Engn Lab, Dept Biochem, Los Angeles, CA 90033 USA
[4] Univ So Calif, Keck Sch Med, Tissue Engn Lab, Dept Mol Biol, Los Angeles, CA 90033 USA
关键词
demineralized bone matrix; bioassay; C2C12; cells; osteoinductivity; alkaline phosphatase;
D O I
10.1016/S0736-0266(03)00005-6
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
A sensitive, rapid, reliable and quantitative method to check the bone forming potential of demineralized bone matrix (DBM) has been developed. The osteoinductivity of the bone morphogenetic proteins (BMPs), present in DBM, can be measured in vitro using a pluripotent myoblast C2C12 cell line. Alkaline phosphatase activity induced by co-incubation of DBM with C2C12 cells was dose-responsive and corresponds to the amount of active BMPs in DBM. Bone forming potential was simultaneously tested in vivo by implanting DBM intra-muscularly in nude rats. ALP activity induced in C2C12 cells, correlated with bone formation in vivo (r = 0.88), determined by alkaline phosphatase activity, mineralization density and histomorphology of the DBM explants. Results from DBM batches, originating from five established Bone Banks, showed good consistency between in vitro and in vivo assays. However, DBM activity varied widely from bank to bank as well as from batch to batch within the same bank. (C) 2003 Orthopaedic Research Society. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:648 / 654
页数:7
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