Roxadustat pre-conditioning and cyclic uniaxial stretching improve tenogenic differentiation potential of human adipose derived mesenchymal stromal cells

IF 2.5 4区 生物学 Q1 ANATOMY & MORPHOLOGY Tissue & cell Pub Date : 2025-02-27 DOI:10.1016/j.tice.2025.102828
Amirah Zulkifli , Hui Yin Nam , Wuey Min Ng , Nor Faissal Yasin , Tunku Kamarul
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Abstract

Tendon injuries represent a significant challenge to treat owing to their limited intrinsic reparative capacity. The use of mesenchymal stem cells (MSC) offers promising alternative therapeutic option to augments tendon repair. It is hypothesised that the activation of hypoxia inducible factor-1 alpha (HIF-1α), could facilitate the tendon repair process by promoting the proliferation and tenogenic differentiation of MSCs. To demonstrate this, a study was conducted incorporating the use of Roxadustat, a specific hypoxia mimetic mediator and cyclic uniaxial stretching at a frequency of 1 Hz and 8 % strain on adipose derived-mesenchymal stromal cells (ADMSCs). Methods: Cellular morphology, proliferation rate, tenogenic protein and gene expression levels from 8 different treatment groups were compared. These groups include untreated ADMSCs (Control), Roxadustat pre-conditioned ADMSCs (ROX), ADMSCs subjected CAY10585 treatment only (CAY), Roxadustat pre-conditioned ADMSCs with CAY10585 inhibition (ROX+CAY), ADMSCs subjected to uniaxial stretching only (S), Roxadustat pre-conditioned ADMSCs with uniaxial stretching (ROX+S), ADMSCs subjected CAY10585 with uniaxial stretching (CAY+S) and primary tenocytes (Tenocytes). Results: ROX+S group exhibited the highest expression of HIF-1α and demonstrated a significant up-regulation of collagen I and III expressions, increasing by 4.9 and 5.6-fold compared to ROX group, respectively. There is a significant increase of SCX, TNC, TNMD, COLI and COLIII expression in this combination treatment group; (SCX= 9.9, TNC= 12.6, TNMD= 7.0, COLI= 8.0 and COLIII= 10.0-fold). Conversely, the expression of the markers markedly reduced with HIF-1α inhibitor CAY10585. However, uniaxial stretching effectively counteracted the inhibitory effects of CAY10585 in the CAY+ S group, resulting in a 3.9-fold increase in SCX expression compared to CAY treatment alone. Conclusion: HIF-1α accumulation promotes superior tenogenic differentiation of ADMSCs, suggesting that the combination of Roxadustat and cyclic uniaxial stretching may be a potential therapeutic mediator in tendon repair strategies.
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罗沙司他预处理和循环单轴拉伸可提高人脂肪间充质基质细胞的成腱分化潜力
肌腱损伤由于其有限的内在修复能力,是治疗的一个重大挑战。间充质干细胞(MSC)的使用为增强肌腱修复提供了有希望的替代治疗选择。假设缺氧诱导因子-1α (HIF-1α)的激活可以通过促进MSCs的增殖和成肌腱分化来促进肌腱修复过程。为了证明这一点,研究人员对脂肪源间充质间质细胞(ADMSCs)进行了一项研究,包括使用Roxadustat(一种特定的模拟缺氧介质)和频率为1 Hz和8 % strain的循环单轴拉伸。方法:比较8个不同处理组的细胞形态、增殖率、成腱蛋白及基因表达水平。这些组包括未经处理的ADMSCs (Control),罗沙司他预处理的ADMSCs (ROX),仅接受CAY10585处理的ADMSCs (CAY),罗沙司他预处理的ADMSCs具有CAY10585抑制作用(ROX+CAY),仅接受单轴拉伸的ADMSCs (S),罗沙司他预处理的ADMSCs具有单轴拉伸(ROX+S),接受CAY10585单轴拉伸的ADMSCs (CAY+S)和原代细胞(tenocytes)。结果:ROX+S组HIF-1α表达最高,I、III胶原表达显著上调,分别较ROX组增加4.9倍、5.6倍。联合治疗组SCX、TNC、TNMD、COLI、COLIII表达明显升高;(SCX= 9.9, TNC= 12.6, TNMD= 7.0, COLI= 8.0, COLIII= 10.0)。相反,HIF-1α抑制剂CAY10585显著降低了这些标志物的表达。然而,单轴拉伸有效抵消了CAY10585在CAY+ S组中的抑制作用,导致SCX表达比单独CAY处理增加3.9倍。结论:HIF-1α的积累促进了ADMSCs的良好的肌腱分化,表明罗沙司他联合循环单轴拉伸可能是肌腱修复策略的潜在治疗介质。
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来源期刊
Tissue & cell
Tissue & cell 医学-解剖学与形态学
CiteScore
3.90
自引率
0.00%
发文量
234
期刊介绍: Tissue and Cell is devoted to original research on the organization of cells, subcellular and extracellular components at all levels, including the grouping and interrelations of cells in tissues and organs. The journal encourages submission of ultrastructural studies that provide novel insights into structure, function and physiology of cells and tissues, in health and disease. Bioengineering and stem cells studies focused on the description of morphological and/or histological data are also welcomed. Studies investigating the effect of compounds and/or substances on structure of cells and tissues are generally outside the scope of this journal. For consideration, studies should contain a clear rationale on the use of (a) given substance(s), have a compelling morphological and structural focus and present novel incremental findings from previous literature.
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