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分析基于胶原的屏障膜骨化与潜在骨缺损之间的细胞相互作用。

Analyses of the Cellular Interactions between the Ossification of Collagen-Based Barrier Membranes and the Underlying Bone Defects.

机构信息

BerlinAnalytix GmbH, 12109 Berlin, Germany.

Clinic and Policlinic for Dermatology and Venereology, University Medical Center Rostock, 18057 Rostock, Germany.

出版信息

Int J Mol Sci. 2023 Apr 6;24(7):6833. doi: 10.3390/ijms24076833.

DOI:10.3390/ijms24076833
PMID:37047808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10095555/
Abstract

Barrier membranes are an essential tool in guided bone Regeneration (GBR), which have been widely presumed to have a bioactive effect that is beyond their occluding and space maintenance functionalities. A standardized calvaria implantation model was applied for 2, 8, and 16 weeks on Wistar rats to test the interactions between the barrier membrane and the underlying bone defects which were filled with bovine bone substitute materials (BSM). In an effort to understand the barrier membrane's bioactivity, deeper histochemical analyses, as well as the immunohistochemical detection of macrophage subtypes (M1/M2) and vascular endothelial cells, were conducted and combined with histomorphometric and statistical approaches. The native collagen-based membrane was found to have ossified due to its potentially osteoconductive and osteogenic properties, forming a "bony shield" overlying the bone defects. Histomorphometrical evaluation revealed the resorption of the membranes and their substitution with bone matrix. The numbers of both M1- and M2-macrophages were significantly higher within the membrane compartments compared to the underlying bone defects. Thereby, M2-macrophages significantly dominated the tissue reaction within the membrane compartments. Statistically, a correlation between M2-macropahges and bone regeneration was only found at 2 weeks post implantationem, while the pro-inflammatory limb of the immune response correlated with the two processes at 8 weeks. Altogether, this study elaborates on the increasingly described correlations between barrier membranes and the underlying bone regeneration, which sheds a light on the understanding of the immunomodulatory features of biomaterials.

摘要

屏障膜是引导骨再生(GBR)的重要工具,人们普遍认为其具有生物活性作用,超出了其封闭和空间维持功能。本研究应用标准化的颅顶植入模型,在 Wistar 大鼠上进行了 2、8 和 16 周的实验,以测试屏障膜与用牛骨替代材料(BSM)填充的骨缺损之间的相互作用。为了了解屏障膜的生物活性,我们进行了更深入的组织化学分析,以及巨噬细胞亚型(M1/M2)和血管内皮细胞的免疫组织化学检测,并结合组织形态计量学和统计方法。由于其潜在的骨传导性和成骨特性,天然胶原基膜发生了骨化,在骨缺损上方形成了一个“骨性盾牌”。组织形态计量学评估显示,膜被吸收并被骨基质取代。与骨缺损相比,膜腔中的 M1 和 M2 巨噬细胞数量明显更高。因此,M2 巨噬细胞在膜腔组织反应中明显占主导地位。统计分析表明,M2 巨噬细胞与骨再生之间仅在植入后 2 周存在相关性,而免疫反应的促炎支与这两个过程在 8 周时相关。总之,本研究阐述了屏障膜与骨再生之间越来越多的描述性关联,这有助于了解生物材料的免疫调节特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d14/10095555/dbccfd744e18/ijms-24-06833-g007.jpg
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