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天然、去细胞化和再接种猪牙芽基质的特性研究。

Characterization of natural, decellularized and reseeded porcine tooth bud matrices.

机构信息

Department of Oral and Maxillofacial Pathology, Division of Craniofacial and Molecular Genetics, Tufts University, Boston, MA 02111, USA.

出版信息

Biomaterials. 2012 Jul;33(21):5287-96. doi: 10.1016/j.biomaterials.2012.04.010. Epub 2012 Apr 30.

Abstract

Dental tissue engineering efforts have yet to identify scaffolds that instruct the formation of bioengineered teeth of predetermined size and shape. Here we investigated whether extracellular matrix (ECM) molecules present in natural tooth scaffolds can provide insight on how to achieve this goal. We describe methods to effectively decellularize and demineralize porcine molar tooth buds, while preserving natural ECM protein gradients. Natural tooth ECM composition was assessed using histological and immunohistochemical (IHC) analyses of fibrillar and basement membrane proteins. Our results showed that Collagen I, Fibronectin, Collagen IV, and Laminin gradients were detected in natural tooth tissues, and retained in decellularized samples. Second harmonic generation (SHG) image analysis and 3D reconstructions were used to show that natural tooth tissue exhibited higher collagen fiber density, and less oriented and less organized collagen fibers, as compared to decellularized tooth tissue. We also found that reseeded decellularized tooth scaffolds exhibited distinctive collagen content and organization as compared to decelluarized scaffolds. Our results show that SHG allows for quantitative assessment of ECM features that are not easily characterized using traditional histological analyses. In summary, our results demonstrate the potential for natural decellularized molar tooth ECM to instruct dental cell matrix synthesis, and lay the foundation for future use of biomimetic scaffolds for dental tissue engineering applications.

摘要

牙组织工程的努力尚未确定支架,以指示预定大小和形状的生物工程牙齿的形成。在这里,我们研究了天然牙支架中存在的细胞外基质(ECM)分子是否可以提供如何实现这一目标的见解。我们描述了有效脱细胞和脱矿化猪磨牙芽的方法,同时保留天然 ECM 蛋白梯度。使用纤维状和基底膜蛋白的组织学和免疫组织化学(IHC)分析评估天然牙 ECM 的组成。我们的结果表明,天然牙组织中检测到胶原 I、纤连蛋白、胶原 IV 和层粘连蛋白梯度,并保留在脱细胞样本中。二次谐波产生(SHG)图像分析和 3D 重建用于表明与脱细胞牙组织相比,天然牙组织具有更高的胶原纤维密度、更少定向和组织化的胶原纤维。我们还发现,与脱细胞支架相比,重新接种的脱细胞牙支架表现出独特的胶原含量和组织。我们的结果表明,SHG 允许对 ECM 特征进行定量评估,而这些特征很难用传统的组织学分析来描述。总之,我们的结果表明,天然脱细胞磨牙 ECM 具有指导牙齿细胞基质合成的潜力,为未来仿生支架在牙科组织工程应用中的应用奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5982/3374342/c838a2066a92/nihms375348f1.jpg

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