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ε-氨基己酸是一种对软骨组织工程有用的纤维蛋白降解抑制剂。

Epsilon-aminocaproic acid is a useful fibrin degradation inhibitor for cartilage tissue engineering.

作者信息

Kupcsik Laszlo, Alini Mauro, Stoddart Martin J

机构信息

Biomaterials and Tissue Engineering Program, AO Research Institute , Davos Platz, Switzerland.

出版信息

Tissue Eng Part A. 2009 Aug;15(8):2309-13. doi: 10.1089/ten.tea.2008.0400.

Abstract

Fibrin is a hydrogel carrier widely used in cartilage tissue engineering. It is rapidly degraded by plasmin, which is produced by the cells. epsilon-Aminocaproic acid (EACA) can be used to inhibit this enzyme and thus save the fibrin carrier. In this study we investigated the effect of EACA on the transforming growth factor beta-1-induced chondrogenic differentiation of human bone marrow-derived mesenchymal stem cells (hMSCs). To assess this, we used the standard pellet culture system, and EACA treatment was compared to an untreated chondrogenic control. To investigate differentiation, real-time RT-PCR was used on chondrocytic marker genes: aggrecan, collagen types II and X, and the SRY-related HMG-box gene 9 (SOX9). Also, specific glycosaminoglycan production was measured. Safranin-O/fast green staining was used to localize proteoglycans and collagens within the pellet. All results concur that EACA did not affect the chondrogenic differentiation process at 5 muM concentration, which is adequate to inhibit fibrin degradation. Therefore, it is a useful plasmin inhibitor for cartilage tissue engineering with hMSCs.

摘要

纤维蛋白是一种广泛应用于软骨组织工程的水凝胶载体。它会被细胞产生的纤溶酶迅速降解。ε-氨基己酸(EACA)可用于抑制这种酶,从而保护纤维蛋白载体。在本研究中,我们调查了EACA对转化生长因子β-1诱导的人骨髓间充质干细胞(hMSCs)软骨分化的影响。为了评估这一点,我们使用了标准的微团培养系统,并将EACA处理组与未处理的软骨分化对照组进行比较。为了研究分化情况,我们对软骨细胞标记基因:聚集蛋白聚糖、II型和X型胶原蛋白以及SRY相关的HMG盒基因9(SOX9)进行了实时RT-PCR检测。此外,还测量了特定糖胺聚糖的产生。番红O/固绿染色用于定位微团内的蛋白聚糖和胶原蛋白。所有结果均表明,在5μM浓度下,EACA不会影响软骨分化过程,该浓度足以抑制纤维蛋白降解。因此,它是一种用于hMSCs软骨组织工程的有用的纤溶酶抑制剂。

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