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Mechanical adaptation of synoviocytes A and B to immobilization and remobilization: a study in the rat knee flexion model.
Journal of Molecular Histology ( IF 2.9 ) Pub Date : 2020-08-10 , DOI: 10.1007/s10735-020-09902-8
Haodong Zhou 1, 2 , Guy Trudel 2, 3 , Odette Laneuville 1, 2
Affiliation  

The objective of this study was to quantify the in vivo response of synoviocytes type A and B in the posterior joint capsule to knee immobilization and remobilization. Also, to correlate the immunohistochemical data with selected mRNA expression in the posterior joint capsule. Forty-two adult male Sprague–Dawley rats had one knee joint immobilized in flexion for durations of 1–4 weeks. Fifteen were harvested after immobilization and 15 were remobilized for 4 weeks. They were analyzed immunohistochemically with CD68 and CD55 antibodies as markers for synoviocytes type A and type B, respectively. Controls were 15 age-matched rats. The remaining 12 rats had their posterior capsule harvested and synoviocyte-specific CD68, CD55, and uridine diphosphoglucose dehydrogenase (UDPGD) mRNA expression was measured. Controls were 12 sham-operated knees. Knee immobilization for 2 weeks significantly increased synoviocytes A:B staining ratio compared to controls (3.88 ± 1.39 vs. 1.83 ± 0.76; p < 0.05). Remobilization for 4 weeks abolished the increase. Remobilization of knees that were immobilized for 1 week also significantly lowered the synoviocytes A:B staining ratios compared to immobilized-only knees (0.66 ± 0.23 vs. 2.19 ± 0.54; p < 0.05) and to controls (0.66 ± 0.23 vs. 1.32 ± 0.29; p < 0.05). Consistent with the immunohistochemistry, mRNA expression of synoviocyte type B-specific CD55 and UDPGD genes were significantly lower in the capsules immobilized for 2 weeks (both p < 0.05). Knee immobilization and remobilization significantly modulated synoviocytes in vivo, stressing their mechanosensitive nature and possible contribution to immobility-induced changes of the joint capsule.



中文翻译:

滑膜细胞A和B对固定和固定的机械适应:在大鼠膝盖屈曲模型中的研究。

这项研究的目的是量化后关节囊中的A型和B型滑膜细胞对膝关节固定和固定的体内反应。同样,将免疫组织化学数据与后关节囊中选定的mRNA表达相关。42只成年雄性Sprague-Dawley大鼠的一只膝关节屈曲固定,持续1-4周。固定后收获15只,固定15只,持续4周。用CD68和CD55抗体分别作为A型和B型滑膜细胞的标记进行了免疫组织化学分析。对照是15只年龄匹配的大鼠。其余12只大鼠的后囊被收获,并且滑膜细胞特异性CD68,CD55和尿苷二磷酸葡萄糖脱氢酶(UDPGD)mRNA表达被测量。对照是12只假手术的膝盖。与对照组相比,膝关节固定2周显着增加了滑膜细胞A:B染色率(3.88±1.39对1.83±0.76; p <0.05)。复员4周取消了增加。与仅固定膝盖相比(0.66±0.23 vs. 2.19±0.54; p <0.05)和对照组(0.66±0.23 vs 1.32± 0.29; p <0.05)。与免疫组织化学一致,滑膜细胞B型特异性CD55和UDPGD基因的mRNA表达在固定化2周的胶囊中显着降低(均p <0.05)。膝盖固定和固定在体内显着调节滑膜细胞,

更新日期:2020-08-11
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