Department of Orthopedic Surgery, Physical Medicine and Rehabilitation, University Hospital Munich, Campus Grosshadern, LMU, Munich, Bavaria, Germany.
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
J Gene Med. 2021 Mar;23(3):e3311. doi: 10.1002/jgm.3311. Epub 2021 Feb 1.
Fragments of subcutaneous adipose tissue that have been genetically modified to express bone morphogenetic protein-2 (BMP-2) regenerate large segmental osseous lesions in rodents. Gene-activated adipose tissue can be implanted into osseous defects without prior cell extraction and cell culture. The present study aimed to explore whether the heterodimers BMP-2/6 or BMP-2/7 exceed the osteoinductive effect of BMP-2 on adipose tissue.
In an in vitro tissue culture system, freshly harvested rat subcutaneous adipose tissue was cultivated in the presence of either BMP-2 or BMP-2/6 or BMP-2/7 at a high (200 ng/ml) and low (50 ng/ml) concentration. Gene expression analysis as well as histological and immunohistochemical methods were applied to test for osteoinduction.
A concentration of 200 ng/ml of homodimeric BMP-2 induced osteogenic differentiation most potently, showing more calcification and a higher expression level of bone markers than both concentrations of BMP-2/6 or -2/7. A concentration of 50 ng/ml of BMP-2 was a significantly stronger osteogenic inducer than both concentrations of BMP-2/6 and the low concentration of BMP-2/7. The most potent heterodimeric driver of osteoinduction was BMP-2/7 at a high concentration, demonstrating effects similar to those of BMP-2 at a low concentration.
Homodimeric BMP-2 evoked osteoinduction within adipose tissue more potently and at a lower concentration than heterodimeric BMP-2/6 or BMP-2/7. This result agrees well with the fact that it might be easier to translate adipose grafts activated by homodimeric BMP-2 clinically. Preclinical in vivo gene transfer studies are necessary to confirm the results of the present study.
经基因修饰表达骨形态发生蛋白-2(BMP-2)的皮下脂肪组织碎片可在啮齿动物中再生大段节段性骨缺损。基因激活的脂肪组织可在无需预先细胞提取和细胞培养的情况下植入骨缺损部位。本研究旨在探讨 BMP-2/6 或 BMP-2/7 异二聚体是否超过 BMP-2 对脂肪组织的成骨诱导作用。
在体外组织培养系统中,将新鲜收获的大鼠皮下脂肪组织在高(200ng/ml)和低(50ng/ml)浓度下分别培养于 BMP-2 或 BMP-2/6 或 BMP-2/7 中。采用基因表达分析以及组织学和免疫组织化学方法检测成骨诱导作用。
浓度为 200ng/ml 的同源二聚体 BMP-2 诱导成骨分化的能力最强,表现出比 BMP-2/6 或 BMP-2/7 的两种浓度更多的钙化和更高的骨标志物表达水平。浓度为 50ng/ml 的 BMP-2 是比 BMP-2/6 的两种浓度和 BMP-2/7 的低浓度更强的成骨诱导剂。浓度为 200ng/ml 的最有效的异二聚体成骨诱导剂是 BMP-2/7,其作用类似于低浓度的 BMP-2。
同源二聚体 BMP-2 在较低浓度下比异二聚体 BMP-2/6 或 BMP-2/7 更强烈地引发脂肪组织的成骨诱导。这一结果与同源二聚体 BMP-2 更易于在临床上转化为激活脂肪移植物的事实相吻合。需要进行临床前体内基因转移研究来证实本研究的结果。