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通过细胞归巢实现解剖形态牙和牙周组织再生。

Anatomically shaped tooth and periodontal regeneration by cell homing.

机构信息

Columbia University College of Dental Medicine, 630 W. 168th St., PH7E - CDM, New York, NY 10032, USA.

出版信息

J Dent Res. 2010 Aug;89(8):842-7. doi: 10.1177/0022034510370803. Epub 2010 May 6.

Abstract

Tooth regeneration by cell delivery encounters translational hurdles. We hypothesized that anatomically correct teeth can regenerate in scaffolds without cell transplantation. Novel, anatomically shaped human molar scaffolds and rat incisor scaffolds were fabricated by 3D bioprinting from a hybrid of poly-epsilon-caprolactone and hydroxyapatite with 200-microm-diameter interconnecting microchannels. In each of 22 rats, an incisor scaffold was implanted orthotopically following mandibular incisor extraction, whereas a human molar scaffold was implanted ectopically into the dorsum. Stromal-derived factor-1 (SDF1) and bone morphogenetic protein-7 (BMP7) were delivered in scaffold microchannels. After 9 weeks, a putative periodontal ligament and new bone regenerated at the interface of rat incisor scaffold with native alveolar bone. SDF1 and BMP7 delivery not only recruited significantly more endogenous cells, but also elaborated greater angiogenesis than growth-factor-free control scaffolds. Regeneration of tooth-like structures and periodontal integration by cell homing provide an alternative to cell delivery, and may accelerate clinical applications.

摘要

细胞递送的牙齿再生遇到了转化障碍。我们假设在没有细胞移植的情况下,支架内可以再生解剖学上正确的牙齿。新型的、解剖形状的人磨牙支架和大鼠切牙支架是通过 3D 生物打印从聚己内酯和羟基磷灰石的混合物中制造的,具有 200 微米直径的互连微通道。在 22 只大鼠中,在切除下颌切牙后将切牙支架原位植入,而将人磨牙支架异位植入背部。基质衍生因子 1(SDF1)和骨形态发生蛋白 7(BMP7)在支架微通道中递送。9 周后,在大鼠切牙支架与天然牙槽骨的界面处出现了牙周韧带和新骨的再生。SDF1 和 BMP7 的递送不仅招募了更多的内源性细胞,而且比生长因子免费的对照支架更能促进血管生成。通过细胞归巢实现牙齿样结构和牙周整合的再生提供了一种替代细胞递送的方法,并可能加速临床应用。

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