Feng Qian, Zhu Meiling, Wei Kongchang, Bian Liming
Division of Biomedical Engineering, the Chinese University of Hong Kong, Hong Kong, the People's Republic of China; Department of Mechanical and Automation Engineering and the Shun Hing Institute of Advanced Engineering, the Chinese University of Hong Kong, Hong Kong, the People's Republic of China.
Division of Biomedical Engineering, the Chinese University of Hong Kong, Hong Kong, the People's Republic of China; Department of Mechanical and Automation Engineering and the Shun Hing Institute of Advanced Engineering, the Chinese University of Hong Kong, Hong Kong, the People's Republic of China; The Chinese University of Hong Kong Shenzhen Research Institute, the People's Republic of China.
PLoS One. 2014 Jun 9;9(6):e99587. doi: 10.1371/journal.pone.0099587. eCollection 2014.
Photocrosslinked methacrylated hyaluronic acid (MeHA) hydrogels support chondrogenesis of encapsulated human mesenchymal stem cells (hMSCs). However, the covalent crosslinks formed via chain polymerization in these hydrogels are hydrolytically non-degradable and restrict cartilage matrix spatial distribution and cell spreading. Meanwhile, cells are known to remodel their surrounding extracellular matrix (ECM) by secreting catabolic enzymes, such as MMPs. Hydrogels that are created with bifunctional crosslinkers containing MMP degradable peptide sequences have been shown to influence hMSC differentiations. However, crosslinks formed in the MMP-degradable hydrogels of these previous studies are also prone to hydrolysis, thereby confounding the effect of MMP-mediated degradation. The objective of this study is to develop a MMP-sensitive but hydrolytically stable hydrogel scaffold and investigate the effect of MMP-mediated hydrogel degradation on the chondrogenesis of the encapsulated hMSCs. Hyaluronic acid macromers were modified with maleimide groups and crosslinked with MMP-cleavable peptides or control crosslinkers containing dual thiol groups. The chondrogenesis of the hMSCs encapsulated in the hydrolytically stable MMP-sensitive HA hydrogels were compared with that of the MMP-insensitive HA hydrogels. It was found that hMSCs encapsulated in the MMP-sensitive hydrogels switched to a more spreaded morphology while cells in the MMP-insensitive hydrogels remained in round shape. Furthermore, hMSCs in the MMP-sensitive hydrogels expressed higher level of chondrogenic marker genes but lower level of hypertrophic genes compared to cells in the MMP-insensitive hydrogels. As a result, more cartilage specific matrix molecules but less calcification was observed in the MMP-degradable hydrogels than in the MMP-insensitive hydrogels. Findings from this study demonstrate that cell-mediated scaffold degradation regulates the chondrogenesis and hypertrophy of hMSCs encapsulated in HA hydrogels.
光交联甲基丙烯酸化透明质酸(MeHA)水凝胶可支持封装的人间充质干细胞(hMSC)的软骨生成。然而,这些水凝胶中通过链式聚合形成的共价交联在水解时不可降解,限制了软骨基质的空间分布和细胞铺展。同时,已知细胞会通过分泌分解代谢酶(如基质金属蛋白酶,MMPs)来重塑其周围的细胞外基质(ECM)。含有MMP可降解肽序列的双功能交联剂制备的水凝胶已被证明会影响hMSC的分化。然而,这些先前研究中在MMP可降解水凝胶中形成的交联也容易水解,从而混淆了MMP介导的降解作用。本研究的目的是开发一种对MMP敏感但水解稳定的水凝胶支架,并研究MMP介导的水凝胶降解对封装的hMSC软骨生成的影响。用马来酰亚胺基团修饰透明质酸大分子单体,并与MMP可裂解肽或含有双硫醇基团的对照交联剂交联。将封装在水解稳定的MMP敏感HA水凝胶中的hMSC的软骨生成与MMP不敏感的HA水凝胶中的进行比较。发现封装在MMP敏感水凝胶中的hMSC转变为更铺展的形态,而MMP不敏感水凝胶中的细胞保持圆形。此外,与MMP不敏感水凝胶中的细胞相比,MMP敏感水凝胶中的hMSC表达更高水平的软骨生成标记基因,但肥大基因水平较低。结果,在MMP可降解水凝胶中观察到比MMP不敏感水凝胶中更多的软骨特异性基质分子,但钙化较少。本研究结果表明,细胞介导的支架降解调节了封装在HA水凝胶中的hMSC的软骨生成和肥大。