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1,25-二羟维生素D及其类似物卡泊三醇在伤口愈合模型中抑制人滑膜细胞和间充质基质细胞的迁移——与糖皮质激素的比较。

1,25(OH)D and its analogue calcipotriol inhibit the migration of human synovial and mesenchymal stromal cells in a wound healing model - A comparison with glucocorticoids.

作者信息

Huovinen Jere, Palosaari Sanna, Pesonen Paula, Huhtakangas Johanna A, Lehenkari Petri

机构信息

Research Unit of Translational Medicine, Medical Research Center Oulu, Oulu University Hospital and University of Oulu, P.O.Box 5000, FI-90014 Oulu, Finland.

Research Unit of Translational Medicine, Medical Research Center Oulu, Oulu University Hospital and University of Oulu, P.O.Box 5000, FI-90014 Oulu, Finland.

出版信息

J Steroid Biochem Mol Biol. 2023 Oct;233:106373. doi: 10.1016/j.jsbmb.2023.106373. Epub 2023 Aug 8.

Abstract

Vitamin D analogue calcipotriol is currently used in the local treatment of psoriasis. However, it also has antiproliferative and anti-inflammatory effects in the cells of the joint - suggesting a possible benefit in local treatment of arthritis. In this study, calcipotriol was studied in different in vitro methods to find out its effect on synovial and mesenchymal stromal cells. Primary human cell lines of osteoarthritis or rheumatoid arthritis patients (five mesenchymal stromal cells, MSC, and four synovial stromal cells, SSC) were cultured to study migration and proliferation of the cells in a wound healing model. The media was supplemented with calcipotriol, 1,25(OH)D, dexamethasone, betamethasone, methylprednisolone or control solution in 1-100 nM concentrations. To see possible toxic effects of calcipotriol, concentrations up to 10 µM in SSCs and MSCs were studied in apoptosis and necrosis assays in four cell lines. Calcipotriol and 1,25(OH)D, as well as the three glucocorticoids, reduced the migration of both SSCs and MSCs. In SSCs, the effect of calcipotriol and 1,25(OH)D was at least as effective as with glucocorticoids, while with MSCs, the glucocorticoids were stronger inhibitors of migration. The antimigratory of calcipotriol and 1,25(OH)D was consistently maintained in 10 µM and 1 µM. Calcipotriol was not toxic to MSCs and SSCs up to concentrations of 10 µM. Calcipotriol, as well as 1,25(OH)D, exerts antimigratory and antiproliferative effects on human SSCs and MSCs of the joint. These effects are not caused by apoptosis or necrosis. Both calcipotriol and 1,25(OH)D have similar effects as glucocorticoids without apparent toxicity, suggesting that calcipotriol might be an eligible candidate to the local treatment of arthritis with a broad therapeutic window.

摘要

维生素D类似物卡泊三醇目前用于银屑病的局部治疗。然而,它在关节细胞中也具有抗增殖和抗炎作用,这表明其在关节炎局部治疗中可能有益。在本研究中,采用不同的体外方法研究卡泊三醇,以了解其对滑膜细胞和间充质基质细胞的影响。培养骨关节炎或类风湿关节炎患者的原代人细胞系(五个间充质基质细胞,MSC,和四个滑膜基质细胞,SSC),以在伤口愈合模型中研究细胞的迁移和增殖。培养基中添加浓度为1-100 nM的卡泊三醇、1,25(OH)D、地塞米松、倍他米松、甲基泼尼松龙或对照溶液。为了观察卡泊三醇可能的毒性作用,在四种细胞系的凋亡和坏死试验中研究了SSC和MSC中高达10 μM的浓度。卡泊三醇、1,25(OH)D以及三种糖皮质激素均降低了SSC和MSC的迁移。在SSC中,卡泊三醇和1,25(OH)D的作用至少与糖皮质激素一样有效,而在MSC中,糖皮质激素是更强的迁移抑制剂。卡泊三醇和1,25(OH)D在10 μM和1 μM时持续保持抗迁移作用。卡泊三醇在浓度高达10 μM时对MSC和SSC无毒。卡泊三醇以及1,25(OH)D对人关节的SSC和MSC具有抗迁移和抗增殖作用。这些作用不是由凋亡或坏死引起的。卡泊三醇和1,25(OH)D具有与糖皮质激素相似的作用且无明显毒性,这表明卡泊三醇可能是关节炎局部治疗的合适候选药物,具有广阔的治疗窗口。

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