Wong Tzyy Yue, Chang Chiung-Hsin, Yu Chen-Hsiang, Huang Lynn L H
Institute of Biotechnology, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan.
Department of Obstetrics and Gynecology, National Cheng Kung University, Tainan, Taiwan.
Aging Cell. 2017 Jun;16(3):451-460. doi: 10.1111/acel.12567.
Hyaluronan (HA), an abundant polysaccharide found in human bodies, plays a role in the mesenchymal stem cells (MSCs) maintenance. We had previously found that HA prolonged the lifespan, and prevented the cellular aging of murine adipose-derived stromal cells. Recently, we had also summarized the potential pathways associated with HA regulation in human MSCs. In this study, we used the human placenta-derived MSCs (PDMSC) to investigate the effectiveness of HA in maintaining the PDMSC. We found that coating the culture surface coated with 30 μg cm of HA (C) led to cluster growth of PDMSC, and maintained a higher number of PDMSC in quiescence compared to those grown on the normal tissue culture surface (T). PDMSC were treated for either 4 (short-term) or 19 (long-term) consecutive passages. PDMSC which were treated with HA for 19 consecutive passages had reduced cell enlargement, preserved MSCs biomarker expressions and osteogenic potential when compared to those grown only on T. The PDMSC transferred to T condition after long-term HA treatment showed preserved replicative capability compared to those on only T. The telomerase activity of the HA-treated PDMSC was also higher than that of untreated PDMSC. These data suggested a connection between HA and MSC maintenance. We suggest that HA might be regulating the distribution of cytoskeletal proteins on cell spreading in the event of quiescence to preserve MSC stemness. Maintenance of MSCs stemness delayed cellular aging, leading to the anti-aging phenotype of PDMSC.
透明质酸(HA)是人体中一种丰富的多糖,在间充质干细胞(MSC)的维持中发挥作用。我们之前发现,HA可延长小鼠脂肪来源的基质细胞的寿命,并防止其细胞衰老。最近,我们还总结了与人类间充质干细胞中HA调节相关的潜在途径。在本研究中,我们使用人胎盘来源的间充质干细胞(PDMSC)来研究HA在维持PDMSC方面的有效性。我们发现,用30μg/cm²的HA包被培养表面(C)会导致PDMSC呈集落生长,并且与在正常组织培养表面(T)上生长的细胞相比,在静止状态下维持了更多数量的PDMSC。对PDMSC进行连续4代(短期)或19代(长期)处理。与仅在T表面生长的细胞相比,连续19代用HA处理的PDMSC细胞增大减少,保留了间充质干细胞生物标志物的表达和成骨潜能。长期HA处理后转移到T条件下的PDMSC与仅在T表面生长的细胞相比,显示出保留的复制能力。HA处理的PDMSC的端粒酶活性也高于未处理的PDMSC。这些数据表明HA与间充质干细胞的维持之间存在联系。我们认为,在静止状态下,HA可能通过调节细胞铺展时细胞骨架蛋白的分布来维持间充质干细胞的干性。维持间充质干细胞的干性可延缓细胞衰老,从而导致PDMSC的抗衰老表型。