Gorji Mona, Ghasemi Nazem, Setayeshmehr Mohsen, Zargar Anooshe, Kazemi Mohammad, Soleimani Mitra, Hashemibeni Batool
Department of Anatomical Sciences and Molecular Biology, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Department of Advanced Medical Technology, Biomaterials Nanaotechnology and Tissue Engineering Group, Isfahan University of Medical Sciences, Isfahan, Iran.
Adv Biomed Res. 2020 Feb 25;9:6. doi: 10.4103/abr.abr_143_19. eCollection 2020.
Nowadays, cartilage tissue engineering is the best candidate for regeneration of cartilage defects. This study evaluates the effect of fibrin/icariin (ICA) nanoparticles (F/I NPs) on chondrogenesis of stem cells.
F/I NPs were characterized by Dynamic Light Scattering DLS. Poly (lactic-co-glycolic) acid (PLGA)-F/I NP scaffold was fabricated and assessed by scanning electron microscope. Human adipose-derived stem cells (hADSCs) were seeded on scaffold and induced for chondrogenesis. After 14 days, cell viability and gene expression were analyzed by the 3-(4, 5- dimethylthiazol-2yl)-2, 5-diphenyltetrazolium bromide (MTT) assay. MTT assay and real-time polymerase chain reaction (RT-PCR).
The size and surface charge of F/I NP were about 28-30 nm and - 17, respectively. The average of pore size of PLGA and PLGA-fibrin/ICA was 230 and 340 μm, respectively. Cell viability of differentiated cells in P/F group was higher than others significantly ( ≤ 0.05). Furthermore, quantitative RT-PCR analysis demonstrated that ICA upregulated cartilaginous-specific gene expression. Furthermore, the results of the expression of type I collagen revealed that ICA downregulated this gene significantly ( < 0.01).
The results indicated that F/I NP could be a potential factor for chondrogenesis of stem cells and downregulation of fibrocartilage marker.
如今,软骨组织工程是软骨缺损再生的最佳选择。本研究评估了纤维蛋白/淫羊藿苷(ICA)纳米颗粒(F/I NPs)对干细胞软骨生成的影响。
通过动态光散射(DLS)对F/I NPs进行表征。制备聚(乳酸-共-乙醇酸)(PLGA)-F/I NP支架,并通过扫描电子显微镜进行评估。将人脂肪来源干细胞(hADSCs)接种在支架上并诱导其软骨生成。14天后,通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法分析细胞活力和基因表达。采用MTT法和实时聚合酶链反应(RT-PCR)。
F/I NP的尺寸和表面电荷分别约为28 - 30 nm和 - 17。PLGA和PLGA-纤维蛋白/ICA的平均孔径分别为230和340μm。P/F组中分化细胞的细胞活力显著高于其他组(≤0.05)。此外,定量RT-PCR分析表明ICA上调了软骨特异性基因表达。此外,I型胶原蛋白表达结果显示ICA显著下调了该基因(<0.01)。
结果表明F/I NP可能是干细胞软骨生成和纤维软骨标志物下调的潜在因素。