Institute for Tissue Engineering and Regenerative Medicine, The Chinese University of Hong Kong (CUHK), Shatin, Hong Kong SAR, China.
School of Biomedical Sciences, CUHK, Shatin, Hong Kong SAR, China.
J Mater Chem B. 2021 Sep 15;9(35):7205-7215. doi: 10.1039/d1tb00268f.
Hyaluronic acid (HA)-based biomaterials have been demonstrated to promote wound healing and tissue regeneration, owing to the intrinsic and important role of HA in these processes. A deeper understanding of the biological functions of HA would enable better informed decisions on applications involving HA-based biomaterial design. HA and fibronectin are both major components of the provisional extracellular matrix (ECM) during wound healing and regeneration. Both biomacromolecules exhibit the same spatiotemporal distribution, with fibronectin possessing direct binding sites for HA. As HA is one of the first components present in the wound healing bed, we hypothesized that HA may be involved in the deposition, and subsequently fibrillogenesis, of fibronectin. This hypothesis was tested by exposing cultures of mesenchymal stromal cells (MSCs), which are thought to be involved in the early phase of wound healing, to high molecular weight HA (HMWHA). The results showed that treatment of human bone marrow derived MSCs (bmMSCs) with exogenous HMWHA increased fibronectin fibril formation during early ECM deposition. On the other hand, partial depletion of endogenous HA led to a drastic impairment of fibronectin fibril formation, despite detectable granular presence of fibronectin in the perinuclear region, comparable to observations made under the well-established ROCK inhibition-mediated impairment of fibronectin fibrillogenesis. These findings suggest the functional involvement of HA in effective fibronectin fibrillogenesis. The hypothesis was further supported by the co-alignment of fibronectin, HA and integrin α5 at sites of ongoing fibronectin fibrillogenesis, suggesting that HA might be directly involved in fibrillar adhesions. Given the essential function of fibronectin in ECM assembly and maturation, HA may play a major enabling role in initiating and propagating ECM deposition. Thus, HA, as a readily available biomaterial, presents practical advantages for ECM-rich tissue formation in tissue engineering and regenerative medicine.
透明质酸(HA)基生物材料由于其在这些过程中的内在重要作用,已被证明可促进伤口愈合和组织再生。更深入地了解 HA 的生物学功能将使我们能够更好地了解基于 HA 的生物材料设计的应用。HA 和纤维连接蛋白都是伤口愈合和再生过程中临时细胞外基质(ECM)的主要成分。这两种生物大分子都具有相同的时空分布,纤维连接蛋白具有直接结合 HA 的结合位点。由于 HA 是伤口愈合床中最早存在的成分之一,我们假设 HA 可能参与纤维连接蛋白的沉积和随后的纤维原纤维形成。这一假设通过暴露于骨髓间充质基质细胞(MSCs)培养物中进行了测试,这些细胞被认为参与了伤口愈合的早期阶段,向其中添加高分子量 HA(HMWHA)。结果表明,用外源性 HMWHA 处理人骨髓来源的间充质基质细胞(bmMSCs)会增加早期 ECM 沉积过程中纤维连接蛋白纤维的形成。另一方面,内源性 HA 的部分耗竭导致纤维连接蛋白纤维的形成严重受损,尽管在核周区域可见纤维连接蛋白的颗粒状存在,这与在广泛建立的 ROCK 抑制介导的纤维连接蛋白纤维原纤维形成受损的情况下的观察结果相当。这些发现表明 HA 参与了纤维连接蛋白的有效纤维原纤维形成。该假说进一步得到了纤维连接蛋白、HA 和整合素 α5 在纤维连接蛋白纤维原纤维形成部位共定位的支持,表明 HA 可能直接参与纤维状黏附。鉴于纤维连接蛋白在 ECM 组装和成熟中的重要功能,HA 可能在启动和传播 ECM 沉积方面发挥主要的促进作用。因此,HA 作为一种现成的生物材料,在组织工程和再生医学中具有促进富含 ECM 的组织形成的实际优势。