Inserm, UMR-S 1229, R-MeS Lab, Nantes, 44042, France; Université de Nantes, UMR-S 1229 R-MeS Lab, UFR odontologie, Nantes, 44042, France; STEMCIS, Besançon, France.
Inserm, UMR-S 1229, R-MeS Lab, Nantes, 44042, France; Université de Nantes, UMR-S 1229 R-MeS Lab, UFR odontologie, Nantes, 44042, France; CHU de Nantes, PHU 4 OTONN, Nantes, 44042, France; CHU de Nantes, clinique de stomatologie et chirurgie maxillo-faciale, Nantes, 44042, France.
J Stomatol Oral Maxillofac Surg. 2019 Nov;120(5):432-442. doi: 10.1016/j.jormas.2019.01.002. Epub 2019 Jan 11.
In craniofacial reconstruction, the gold standard procedure for bone regeneration is the autologous bone graft (BG). However, this procedure requiring bone harvesting is a source of morbidity. Bone substitutes, such as biphasic calcium phosphate (BCP), represent an interesting alternative but are not sufficient for bone healing in hypoplastic conditions. In such conditions, osteoprogenitors are essential to provide osteoinduction. Previous studies have shown that BCP associated with total bone marrow (TBM) provides same bone reconstruction as bone graft in a rat model of calvaria defect. Furthermore, adipose tissue stromal vascular fraction (SVF) seems to be another promising source of osteoprogenitor cells that can be used intra-operatively. This study aimed to combine, intra-operative BCP-based bone tissue engineering strategies with TBM or SVF from human sources.
5 mm critical-size calvaria defects were performed in 18 nude rat. The defects were filled with intra-operative bone tissue engineering procedures: human BG, human TBM + BCP, human SVF + BCP and, rat TBM + BCP. Animals were sacrificed 8 weeks after implantation and calvaria were processed for histological and radiological examinations. Implanted cells were labelled with a fluorochrome.
Micro-CT analysis revealed partial repair of bone defect. Only hBG significantly succeeded in healing the defect (43.1%). However, low rate of newly formed bone tissue was observed in all tissue engineering conditions (hTBM, hSVF, ratTBM).
The lack of bone formation observed in this study could possibly be attributed to the model.
This study combined with a literature analysis show the stringency of the nude rat calvaria model in term of bone regeneration.
在颅面重建中,骨再生的金标准程序是自体骨移植(BG)。然而,这种需要进行骨采集的手术会带来一定的发病率。骨替代物,如双相磷酸钙(BCP),是一种很有前途的替代品,但在骨发育不全的情况下,其骨愈合效果并不理想。在这种情况下,成骨前体细胞对于提供成骨诱导是必不可少的。先前的研究表明,BCP 与全骨髓(TBM)联合应用在颅骨缺损的大鼠模型中可提供与骨移植相同的骨重建效果。此外,脂肪组织基质血管部分(SVF)似乎是另一种有前途的成骨前体细胞来源,可以在手术中使用。本研究旨在将基于 BCP 的术中骨组织工程策略与来自人体的 TBM 或 SVF 相结合。
在 18 只裸鼠中进行了 5mm 临界尺寸的颅骨缺损。通过术中骨组织工程程序对这些缺陷进行填充:人 BG、人 TBM+BCP、人 SVF+BCP 和大鼠 TBM+BCP。植入 8 周后处死动物,对颅骨进行组织学和影像学检查。植入的细胞用荧光染料标记。
微 CT 分析显示骨缺损部分修复。只有 hBG 能显著成功地治愈缺陷(43.1%)。然而,在所有组织工程条件下(hTBM、hSVF、ratTBM),新形成的骨组织率都很低。
本研究中观察到的骨形成不足可能归因于模型。
本研究结合文献分析表明,裸鼠颅骨模型在骨再生方面的严格性。