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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >In vitro culture and characterization of alveolar bone osteoblasts isolated from type 2 diabetics
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In vitro culture and characterization of alveolar bone osteoblasts isolated from type 2 diabetics

机译:从2型糖尿病患者中分离出牙槽骨成骨细胞的体外培养和鉴定

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In order to understand the mechanisms of poor osseointegration following dental implants in type 2 diabetics, it is important to study the biological properties of alveolar bone osteoblasts isolated from these patients. We collected alveolar bone chips under aseptic conditions and cultured them in vitro using the tissue explants adherent method. The biological properties of these cells were characterized using the following methods: alkaline phosphatase (ALP) chemical staining for cell viability, Alizarin red staining for osteogenic characteristics, MTT test for cell proliferation, enzyme dynamics for ALP contents, radio-immunoassay for bone gla protein (BGP) concentration, and ELISA for the concentration of type I collagen (COL-I) in the supernatant. Furthermore, we detected the adhesion ability of two types of cells from titanium slices using non-specific immunofluorescence staining and cell count. The two cell forms showed no significant difference in morphology under the same culture conditions. However, the alveolar bone osteoblasts received from type 2 diabetic patients had slower growth, lower cell activity and calcium nodule formation than the normal ones. The concentration of ALP, BGP and COL-I was lower in the supernatant of alveolar bone osteoblasts received from type 2 diabetic patients than in that received from normal subjects (P < 0.05). The alveolar bone osteoblasts obtained from type 2 diabetic patients can be successfully cultured in vitro with the same morphology and biological characteristics as those from normal patients, but with slower growth and lower concentration of specific secretion and lower combining ability with titanium than normal ones.
机译:为了了解2型糖尿病患者种植牙后骨整合不良的机制,重要的是研究从这些患者中分离出的牙槽骨成骨细胞的生物学特性。我们在无菌条件下收集牙槽骨碎片,并使用组织外植体粘附方法在体外进行培养。使用以下方法表征这些细胞的生物学特性:碱性磷酸酶(ALP)化学染色法测定细胞活力,茜素红染色法测定成骨特性,MTT法测定细胞增殖,酶动力学测定ALP含量,放射免疫法测定骨gla蛋白(BGP)浓度,以及用于上清液中I型胶原蛋白(COL-1)浓度的ELISA。此外,我们使用非特异性免疫荧光染色和细胞计数检测了钛切片中两种类型细胞的粘附能力。在相同的培养条件下,两种细胞形式在形态上均无显着差异。但是,与正常人相比,从2型糖尿病患者中获得的牙槽骨成骨细胞的生长较慢,细胞活性较低,钙结节形成较慢。从2型糖尿病患者接受的牙槽骨成骨细胞上清液中ALP,BGP和COL-1的浓度低于正常受试者(P <0.05)。从2型糖尿病患者获得的牙槽骨成骨细胞可以成功地体外培养,具有与正常患者相同的形态和生物学特征,但与正常人相比,其生长速度较慢,特异性分泌物的浓度较低,与钛的结合能力较低。

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