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他克莫司或西罗莫司对血管壁细胞黏附的影响:体外对照比较研究。

Effects of Tacrolimus or Sirolimus on the adhesion of vascular wall cells: Controlled in-vitro comparison study.

作者信息

Krüger-Genge A, Hiebl B, Franke R P, Lendlein A, Jung F

机构信息

Institute of Biomaterial Science and Berlin-Brandenburg Center for Regenerative Therapies, Helmholtz-Zentrum Geesthacht, Teltow, Germany.

Institute for Animal Hygiene, Animal Welfare and Farm Animal Behavior, University of Veterinary Medicine Hannover, Hannover, Germany.

出版信息

Clin Hemorheol Microcirc. 2017;67(3-4):309-318. doi: 10.3233/CH-179211.

Abstract

In drug eluting stents the cytostatic drugs Sirolimus or Tacrolimus are used to inhibit blood vessel restenosis by limiting the proliferation of smooth muscle cells. However, the cytostatic activity of both drugs was shown to be not cell specific and could also affect the stent endothelialisation, respectively. Currently, only limited in vitro data are available about the impact of Sirolimus and Tacrolimus on endothelial cell proliferation over a broad concentration range. To answer this question the following study was performed.Commercially obtained HUVEC were expanded with DMEM cell culture medium (GIBCO, Germany) supplemented with 5 vol% fetal calf serum on non-coated regular polystyrene-based 24-multiwell plates. For drug testings 2×104 cells/cm2 were seeded and grown for 24 h until 30-40% of the multiwell surfaces were covered and then exposed to Sirolimus (1.0×10-11 - 1.0×10-5 mol/l) or Tacrolimus (2.0×10-8 - 6.2×10-5 mol/l), both dissolved in DMSO. 12, 24 and 48 h after adding the drugs cell numbers per area were quantified by counting the cells in six wells with four fields of view per well, representing 0.6 mm2, using a confocal laser microscope.After 48 h of cell growth in the drug-free cell culture medium, the HUVEC number increased from 2.0×104 to 3.55×104 cells/cm2 (mean cell doubling time: 53.6 h, n = 6). At lower concentrations (≤2.0×10-6 mol/l) Tacrolimus reduced the number of adherent HUVEC significantly less than Sirolimus (p < 0.05). However, at higher concentrations (≥2.07×10-5 mol/l) the effect of Tacrolimus on the number of adherent endothelial cells was significantly greater than that of Sirolimus (p < 0.05). At the highest concentration applied (6.22×10-5 mol/l), Tacrolimus induced detachment of all HUVECs within 12 h after drug application. The number of adherent HUVEC decreased only slightly (about 9%) after Sirolimus application at the highest concentration (1.09×10-5 mol/l).These data show that in a non-flow model the cytostatic drug Tacrolimus reduced the number of adherent endothelial cells less than Sirolimus, as long as the drug concentration did not surpass 10-6 mol/l. At the limits of solubility, Sirolimus (1×10-5 mol/l) reduced the number of adherent endothelial cells less than Tacrolimus (6×10-5 mol/l), which induced detachment of endothelial cells.

摘要

在药物洗脱支架中,使用细胞生长抑制药物西罗莫司或他克莫司通过限制平滑肌细胞的增殖来抑制血管再狭窄。然而,这两种药物的细胞生长抑制活性并非细胞特异性的,也会分别影响支架的内皮化。目前,关于西罗莫司和他克莫司在较宽浓度范围内对内皮细胞增殖影响的体外数据有限。为回答这个问题,进行了以下研究。

通过在未包被的常规聚苯乙烯材质的24孔板中,用添加了5%体积分数胎牛血清的DMEM细胞培养基(德国GIBCO公司)扩增从商业途径获得的人脐静脉内皮细胞(HUVEC)。进行药物测试时,以2×10⁴个细胞/cm²的密度接种细胞并培养24小时,直至多孔板表面30 - 40%被覆盖,然后将细胞暴露于溶解在二甲基亚砜(DMSO)中的西罗莫司(1.0×10⁻¹¹ - 1.0×10⁻⁵mol/L)或他克莫司(2.0×10⁻⁸ - 6.2×10⁻⁵mol/L)。添加药物后12、24和48小时,使用共聚焦激光显微镜通过对六个孔中每个孔四个视野(代表0.6mm²)的细胞进行计数来量化单位面积内的细胞数量。

在无药物的细胞培养基中培养48小时后,HUVEC数量从2.0×10⁴个细胞/cm²增加到3.55×10⁴个细胞/cm²(平均细胞倍增时间:53.6小时,n = 6)。在较低浓度(≤2.0×10⁻⁶mol/L)时,他克莫司对贴壁HUVEC数量的减少作用明显小于西罗莫司(p < 0.05)。然而,在较高浓度(≥2.07×10⁻⁵mol/L)时,他克莫司对贴壁内皮细胞数量的影响明显大于西罗莫司(p < 0.05)。在应用的最高浓度(6.22×10⁻⁵mol/L)下,他克莫司在给药后12小时内导致所有HUVEC脱离。在最高浓度(1.09×10⁻⁵mol/L)下应用西罗莫司后,贴壁HUVEC数量仅略有减少(约减少9%)。

这些数据表明,在非流动模型中,只要药物浓度不超过10⁻⁶mol/L,细胞生长抑制药物他克莫司对贴壁内皮细胞数量的减少作用小于西罗莫司。在溶解度极限时,西罗莫司(1×10⁻⁵mol/L)对贴壁内皮细胞数量的减少作用小于他克莫司(6×10⁻⁵mol/L),后者会导致内皮细胞脱离。

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