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纳米载体融合骨形态发生蛋白-4 增强体内成骨作用。

Enhanced in vivo osteogenesis by nanocarrier-fused bone morphogenetic protein-4.

机构信息

Department of Orthopedic Surgery, Okayama University, Kita-ku, Okayama, Japan.

出版信息

Int J Nanomedicine. 2013;8:1349-60. doi: 10.2147/IJN.S44124. Epub 2013 Apr 9.

Abstract

PURPOSE

Bone defects and nonunions are major clinical skeletal problems. Growth factors are commonly used to promote bone regeneration; however, the clinical impact is limited because the factors do not last long at a given site. The introduction of tissue engineering aimed to deter the diffusion of these factors is a promising therapeutic strategy. The purpose of the present study was to evaluate the in vivo osteogenic capability of an engineered bone morphogenetic protein-4 (BMP4) fusion protein.

METHODS

BMP4 was fused with a nanosized carrier, collagen-binding domain (CBD), derived from fibronectin. The stability of the CBD-BMP4 fusion protein was examined in vitro and in vivo. Osteogenic effects of CBD-BMP4 were evaluated by computer tomography after intramedullary injection without a collagen-sponge scaffold. Recombinant BMP-4, CBD, or vehicle were used as controls. Expressions of bone-related genes and growth factors were compared among the groups. Osteogenesis induced by CBD-BMP4, BMP4, and CBD was also assessed in a bone-defect model.

RESULTS

In vitro, CBD-BMP4 was retained in a collagen gel for at least 7 days while BMP4 alone was released within 3 hours. In vivo, CBD-BMP4 remained at the given site for at least 2 weeks, both with or without a collagen-sponge scaffold, while BMP4 disappeared from the site within 3 days after injection. CBD-BMP4 induced better bone formation than BMP4 did alone, CBD alone, and vehicle after the intramedullary injection into the mouse femur. Bone-related genes and growth factors were expressed at higher levels in CBD-BMP4-treated mice than in all other groups, including BMP4-treated mice. Finally, CBD-BMP4 potentiated more bone formation than did controls, including BMP4 alone, when applied to cranial bone defects without a collagen scaffold.

CONCLUSION

Altogether, nanocarrier-CBD enhanced the retention of BMP4 in the bone, thereby promoting augmented osteogenic responses in the absence of a scaffold. These results suggest that CBD-BMP4 may be clinically useful in facilitating bone formation.

摘要

目的

骨缺损和骨不连是主要的临床骨骼问题。生长因子常用于促进骨再生;然而,由于这些因子在特定部位不能持续很长时间,因此其临床效果有限。引入旨在阻止这些因子扩散的组织工程学是一种很有前途的治疗策略。本研究的目的是评估工程化骨形态发生蛋白 4(BMP4)融合蛋白的体内成骨能力。

方法

将 BMP4 与源自纤连蛋白的纳米载体、胶原结合结构域(CBD)融合。在体外和体内检查 CBD-BMP4 融合蛋白的稳定性。通过不使用胶原海绵支架进行髓内注射后,通过计算机断层扫描评估 CBD-BMP4 的成骨作用。重组 BMP-4、CBD 或载体用作对照。比较各组之间与骨相关的基因和生长因子的表达。还在骨缺损模型中评估了 CBD-BMP4、BMP4 和 CBD 诱导的成骨作用。

结果

在体外,CBD-BMP4 在胶原凝胶中至少保留 7 天,而单独的 BMP4 在 3 小时内释放。在体内,CBD-BMP4 至少在有或没有胶原海绵支架的情况下,在注射部位保留至少 2 周,而 BMP4 在注射后 3 天内从注射部位消失。与单独使用 BMP4、CBD 或载体相比,CBD-BMP4 经小鼠股骨髓内注射后诱导的骨形成更好。与所有其他组(包括 BMP4 处理组)相比,CBD-BMP4 处理的小鼠中表达的与骨相关的基因和生长因子水平更高。最后,当不使用胶原支架应用于颅骨缺损时,CBD-BMP4 比单独使用 BMP4 或其他对照组更能促进骨形成。

结论

总之,纳米载体-CBD 增强了 BMP4 在骨中的保留,从而在没有支架的情况下促进了增强的成骨反应。这些结果表明,CBD-BMP4 可能在促进骨形成方面具有临床应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c21/3626372/015336b06d2b/ijn-8-1349f1.jpg

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