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基于纳米凝胶的支架递送前列腺素E(2)受体特异性激动剂并联合低剂量生长因子可治愈小鼠的临界尺寸骨缺损。

Nanogel-based scaffold delivery of prostaglandin E(2) receptor-specific agonist in combination with a low dose of growth factor heals critical-size bone defects in mice.

作者信息

Kamolratanakul Paksinee, Hayata Tadayoshi, Ezura Yoichi, Kawamata Aya, Hayashi Chikako, Yamamoto Yuka, Hemmi Hiroaki, Nagao Masashi, Hanyu Ryo, Notomi Takuya, Nakamoto Tetsuya, Amagasa Teruo, Akiyoshi Kazunari, Noda Masaki

机构信息

Tokyo Medical and Dental University, Tokyo, Japan.

出版信息

Arthritis Rheum. 2011 Apr;63(4):1021-33. doi: 10.1002/art.30151.

Abstract

OBJECTIVE

Regeneration of bone requires the combination of appropriate drugs and an appropriate delivery system to control cell behavior. However, the delivery of multiple drugs to heal bone is complicated by the availability of carriers. The aim of this study was to explore a new system for delivery of a selective EP4 receptor agonist (EP4A) in combination with low-dose bone morphogenetic protein 2 (BMP-2).

METHODS

Combined delivery of EP4A and BMP-2 was carried out with a nanogel-based scaffold in the shape of a disc, to repair critical-size circle-shaped bone defects in calvariae that otherwise did not heal spontaneously.

RESULTS

Combination treatment with EP4A and low-dose BMP-2 in nanogel efficiently activated bone cells to regenerate calvarial bone by forming both outer and inner cortical plates as well as bone marrow tissue to regenerate a structure similar to that of intact calvaria. EP4A enhanced low-dose BMP-2-induced cell differentiation and activation of transcription events in osteoblasts.

CONCLUSION

These data indicate that combined delivery of EP4A and low-dose BMP-2 via nanogel-based hydrogel provides a new system for bone repair.

摘要

目的

骨再生需要合适的药物与适当的递送系统相结合来控制细胞行为。然而,多种药物用于骨愈合的递送因载体的可用性而变得复杂。本研究的目的是探索一种新的系统,用于联合递送选择性EP4受体激动剂(EP4A)和低剂量骨形态发生蛋白2(BMP-2)。

方法

采用圆盘状纳米凝胶基支架实现EP4A和BMP-2的联合递送,以修复颅骨中临界尺寸的圆形骨缺损,否则这些缺损不会自发愈合。

结果

纳米凝胶中EP4A与低剂量BMP-2联合治疗通过形成外层和内层皮质板以及骨髓组织,有效激活骨细胞以再生颅骨,从而再生出与完整颅骨相似的结构。EP4A增强了低剂量BMP-2诱导的成骨细胞分化和转录事件激活。

结论

这些数据表明,通过纳米凝胶基水凝胶联合递送EP4A和低剂量BMP-2为骨修复提供了一种新系统。

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