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在全髋关节置换术(THR)无菌性松动时,巨噬细胞集落刺激因子(M-CSF)在假体周围组织的滑膜样膜中增加。

Macrophage-colony stimulating factor (M-CSF) is increased in the synovial-like membrane of the periprosthetic tissues in the aseptic loosening of total hip replacement (THR).

作者信息

Xu J W, Konttinen Y T, Waris V, Pätiälä H, Sorsa T, Santavirta S

机构信息

ORTON Research Institute, Invalid Foundation, and Department of Anatomy, Institute of Biomedicine, University of Helsinki, Finland.

出版信息

Clin Rheumatol. 1997 May;16(3):243-8. doi: 10.1007/BF02238958.

Abstract

The aim of the study was to assess the eventual presence, cellular localization and extent of expression of the osteoclast activating cytokine M-CSF (CSF-1) in the periprosthetic tissues around loose total hip replacement (THR). Synovial-like membrane was obtained from the implant-to-bone interface and pseudocapsule from ten total hip revisions performed for aseptic loosening and compared to ten hip synovial tissue samples obtained from ten patients who had primary THR for osteoarthritis. Avidin-biotinperoxidase complex (ABC) and alkaline phosphatase-anti-alkaline phosphatase (APAAP) methods were used for staining and VIDAS image analysis for quantification. M-CSF was mainly produced by macrophages, which often contained wear particles, but also by some fibroblasts and vascular endothelial cells. The number of cells containing (per one mm2 tissue) clearly increased in the interface (1585 +/- 212; p < 0.01) and pseudocapsular (1456 +/- 248; p < 0.01) tissue compared to synovial tissue (543 +/- 118). The present findings suggest, that inflammatory foreign-body type of response enhances expression of M-CSF in cases of aseptic loosening of THR. M-CSF produced in the synovial-like membrane in the implant-bone interface may contribute to activation of osteoclasts in periprosthetic bone and thus to loosening.

摘要

本研究的目的是评估破骨细胞激活细胞因子M-CSF(CSF-1)在松动全髋关节置换术(THR)周围假体周围组织中的最终存在情况、细胞定位及表达程度。从10例因无菌性松动而进行的全髋关节翻修手术的植入物与骨界面处获取滑膜样组织,从假体囊获取假包膜,并与10例因骨关节炎接受初次THR手术的患者的10份髋关节滑膜组织样本进行比较。采用抗生物素蛋白-生物素过氧化物酶复合物(ABC)法和碱性磷酸酶-抗碱性磷酸酶(APAAP)法进行染色,并使用VIDAS图像分析进行定量分析。M-CSF主要由巨噬细胞产生,这些巨噬细胞通常含有磨损颗粒,一些成纤维细胞和血管内皮细胞也可产生M-CSF。与滑膜组织(543±118)相比,界面组织(1585±212;p<0.01)和假包膜组织(1456±248;p<0.01)中含M-CSF的细胞数量(每平方毫米组织)明显增加。目前的研究结果表明,在THR无菌性松动的情况下,炎症性异物反应会增强M-CSF的表达。植入物-骨界面处滑膜样组织中产生的M-CSF可能有助于假体周围骨中破骨细胞的激活,从而导致松动。

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