Prisell P T, Edwall D, Lindblad J B, Levinovitz A, Norstedt G
Center for Biotechnology, NOVUM S-14157, Huddinge, Sweden.
Calcif Tissue Int. 1993 Sep;53(3):201-5. doi: 10.1007/BF01321838.
Bone formation was studied after intramuscular implantation of demineralized bone matrix. Ash weight determinations were used to verify the bone-forming ability of implants, and confirmed that no bone was formed when nonactive implants (stripped of their bone-forming ability) were used. A solution hybridization/RNase protection assay was used for the detection of specific mRNA transcripts in the implants and surrounding tissue. Analysis of insulin-like growth factor I (IGF-I) mRNA showed a transient increase peaking on day 3 following implantation. Radioimmunoassay (RIA) for IGF-I-like immunoreactivity indicated a corresponding increase of IGF-I peptide in extracts from the implants at that time point. IGF-II mRNA and alkaline phosphatase mRNA reached highest levels around day 11 following implantation. Bone formation in old rats, 50 weeks of age, was associated with lower IGF-I mRNA levels 3 days after implantation compared with young animals. IGF-II mRNA levels were also affected and tended to be higher 12 days after implantation compared with young animals. These results indicate that IGFs could be paracrine or autocrine factors in the bone-forming process. During this process, IGF-I mRNA is expressed at an early stage, in correlation with the recruitment and proliferation of surrounding mesenchymal cells, whereas IGF-II mRNA is activated significantly later, correlating to the beginning of the actual calcifying process during endochondral bone formation.
在脱矿骨基质肌内植入后对骨形成进行了研究。通过测定灰重来验证植入物的骨形成能力,并证实当使用无活性植入物(丧失其骨形成能力)时不会形成骨。采用溶液杂交/RNase保护分析法检测植入物及周围组织中的特异性mRNA转录本。胰岛素样生长因子I(IGF-I)mRNA分析显示,植入后第3天出现短暂升高并达到峰值。对IGF-I样免疫反应性的放射免疫测定(RIA)表明,在该时间点植入物提取物中的IGF-I肽相应增加。IGF-II mRNA和碱性磷酸酶mRNA在植入后第11天左右达到最高水平。与年轻动物相比,50周龄的老年大鼠在植入后3天骨形成与较低的IGF-I mRNA水平相关。IGF-II mRNA水平也受到影响,与年轻动物相比,植入后12天往往更高。这些结果表明,IGF可能是骨形成过程中的旁分泌或自分泌因子。在此过程中,IGF-I mRNA在早期表达,与周围间充质细胞的募集和增殖相关,而IGF-II mRNA在软骨内骨形成过程中实际钙化过程开始时显著激活,激活时间明显较晚。