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透明质酸钠补充培养基作为一种新型人间充质干细胞软骨分化培养基模型用于筛选潜在的软骨修复疗法。

Sodium Hyaluronate Supplemented Culture Media as a New hMSC Chondrogenic Differentiation Media-Model for Screening of Potential Cartilage Repair Therapies.

作者信息

Monaco Graziana, El Haj Alicia Jennifer, Alini Mauro, Stoddart Martin James

机构信息

AO Research Institute Davos, Davos, Switzerland.

School of Pharmacy and Bioengineering, Faculty of Medicine and Health Sciences, Keele University, Guy Hilton Research Centre, Thornburrow Drive, Stoke-on-Trent, United Kingdom.

出版信息

Front Bioeng Biotechnol. 2020 Mar 31;8:243. doi: 10.3389/fbioe.2020.00243. eCollection 2020.

Abstract

Surgical strategies to treat articular cartilage injury such as microfracture, expose human bone marrow stem cells (hMSCs) to synovial fluid and its components. High molecular weight hyaluronan (hMwt HA) is one of the most abundant bioactive macromolecules of healthy synovial fluid (hSF) and it plays an important role in the protection of opposing articular cartilage surfaces within the synovial joint. Although hMwt HA has been extensively used to attempt the engineering of the cartilage tissue, its effect as media supplement has not been established. Indeed, current media are often simple in their composition and doesn't recapitulate the rheological and biological features of hSF. In addition, critical molecules that can potentially change the chondrogenic behavior of hBMSCs to make the results more predictive of the real outcome, are lacking. In order to be one step closer to the physiology of hSF, a new culture media supplemented with physiological level of hMwt HA was developed and the effect of the hMwt HA on the chondrogenesis of hMSCs that would be present in a traumatic defect after marrow stimulation techniques, was investigated. hBMSC-seeded fibrin-polyurethane constructs were cultured in a serum free chondropermissive control medium (HA- TGFβ-). This medium was further supplemented with 10 ng/mL TGFβ1 (HA- TGFβ+) or 2 mg/ml hMwt HA 1.8 MDa (HA+ TGFβ-) or both (HA+ TGFβ+). Alternatively, 1 MDa HA was mixed with the fibrin at 0.2 mg/ml (HASc TGFβ+). The effect of hMwt HA on hMSC differentiation was investigated at the gene expression level by RT-qPCR and total DNA, sulfated glycosaminoglycans and Safranin O staining were evaluated. Addition of hMwt HA to the culture media, significantly increased the synthesis of sulfated glycosaminoglycans, especially in the early days of chondrogenesis, and reduced the upregulation of the hypertrophic cartilage marker collagen X. hMwt HA added inside the fibrin gel(HASc TGF+) led to the best matrix deposition. hMwt HA can be one key medium component in a more reliable system to reduce artifacts, enable more accurate pre-screening of potential cartilage repair therapies and reduce the need for animal studies.

摘要

治疗关节软骨损伤的手术策略,如微骨折,会使人类骨髓干细胞(hMSCs)暴露于滑液及其成分中。高分子量透明质酸(hMwt HA)是健康滑液(hSF)中最丰富的生物活性大分子之一,在保护滑膜关节内相对的关节软骨表面方面发挥着重要作用。尽管hMwt HA已被广泛用于尝试软骨组织工程,但它作为培养基补充剂的效果尚未得到证实。事实上,目前的培养基成分往往很简单,无法重现hSF的流变学和生物学特性。此外,缺乏能够潜在改变hBMSCs软骨形成行为从而使结果更能预测实际效果的关键分子。为了更接近hSF的生理状态,开发了一种补充生理水平hMwt HA的新型培养基,并研究了hMwt HA对骨髓刺激技术后创伤性缺损中存在的hMSCs软骨形成的影响。将接种hBMSC的纤维蛋白-聚氨酯构建体在无血清软骨诱导对照培养基(HA - TGFβ -)中培养。该培养基进一步补充10 ng/mL TGFβ1(HA - TGFβ +)或2 mg/ml 1.8 MDa的hMwt HA 1(HA + TGFβ -)或两者(HA + TGFβ +)。或者,将1 MDa HA与纤维蛋白以0.2 mg/ml混合(HASc TGFβ +)。通过RT - qPCR在基因表达水平上研究hMwt HA对hMSC分化的影响,并评估总DNA、硫酸化糖胺聚糖和番红O染色。向培养基中添加hMwt HA显著增加了硫酸化糖胺聚糖的合成,尤其是在软骨形成的早期,并降低了肥大软骨标志物胶原蛋白X的上调。添加到纤维蛋白凝胶内的hMwt HA(HASc TGF +)导致最佳的基质沉积。hMwt HA可以成为更可靠系统中的一个关键培养基成分,以减少假象,实现对潜在软骨修复疗法更准确的预筛选,并减少动物研究的需求。

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