Department of Health Sciences, Sagrado Coração University - USC, Rua Irmã Arminda 10-50, 17011-160, Bauru, SP, Brazil.
Department of Basic Sciences, São Paulo State University (Unesp), School of Dentistry, Rua José Bonifácio 1193, 16015-050, Araçatuba, SP, Brazil.
Mater Sci Eng C Mater Biol Appl. 2020 Feb;107:110229. doi: 10.1016/j.msec.2019.110229. Epub 2019 Oct 11.
Knowledge about the action of immune system in the recognition of biomaterials has been extremely helpful when it comes about understanding host response and biomaterials' fate in human body. This study aimed to investigate inflammatory response and macrophage polarization during bone healing process of rat's calvaria critical defects using different bone materials in order to evaluate their influence on bone repair and on the quality of the newly formed bone tissue. Eighty male albinus Wistar rats underwent surgical procedure for the confectioning of a 5-mm diameter bone defect in their right parietal bone, and divided in four groups (n = 20 each), according the biomaterial: AG - Control, particulate intramembranous autogenous bone graft, HA/TCP - particulate biphasic calcium phosphate with HA/TCP (60/40), DBB - particulate deproteinized bovine bone, VC - particulate bioactive vitroceramic. After 3, 7, 21, and 45 days, the specimens were removed and prepared for microcomputed tomography (microCT), light and polarized microscopy, immunohistochemical analysis, and histomorphometry. No significant differences were detected considering percentage of leukocytes among the groups and periods, as well as in relation to immunolabeling for inflammatory (M1) and reparative (M2) macrophages. However, immunolabeling for bone marker indicated a delayed osteoblast differentiation in VC group, resulting in a decrease in mineralized bone matrix parameters in this group, revealed by microCT. In addition, AG and HA/TCP presented a satisfactory bone collagenous content. Despite the distinct origins and physicochemical properties of the tested biomaterials, they presented similar immune-inflammatory responses in the present experimental model, influencing bone-related proteins and bone quality, which must be considered according to their use.
当涉及到理解宿主反应和生物材料在人体中的命运时,关于免疫系统在识别生物材料方面的作用的知识是非常有帮助的。本研究旨在通过使用不同的骨材料来研究大鼠颅骨临界缺损骨愈合过程中的炎症反应和巨噬细胞极化,以评估它们对骨修复和新形成的骨组织质量的影响。80 只雄性白化 Wistar 大鼠在其右侧顶骨上进行手术,制作 5mm 直径的骨缺损,并根据生物材料分为四组(每组 20 只):AG-对照、颗粒状膜内自体骨移植物、HA/TCP-颗粒状双相磷酸钙(HA/TCP60/40)、DBB-颗粒状脱蛋白牛骨、VC-颗粒状生物活性 vitroceramic。在 3、7、21 和 45 天后,取出标本并进行微计算机断层扫描(microCT)、光镜和偏光显微镜、免疫组织化学分析和组织形态计量学分析。在各组和各时期的白细胞百分比以及与炎症(M1)和修复(M2)巨噬细胞的免疫标记物方面,未检测到显著差异。然而,骨标志物的免疫标记物表明 VC 组成骨细胞分化延迟,导致该组矿化骨基质参数减少,microCT 显示。此外,AG 和 HA/TCP 具有令人满意的骨胶原含量。尽管测试的生物材料具有不同的起源和物理化学性质,但它们在本实验模型中表现出相似的免疫炎症反应,影响与骨相关的蛋白质和骨质量,这必须根据它们的用途加以考虑。