Gao F, Yang C X, Mo W, Liu Y W, He Y Q
Department of Laboratory Medicine, No. 6 People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200233, PR China.
Clin Invest Med. 2008;31(3):E106-16. doi: 10.25011/cim.v31i3.3467.
To determine if oligosaccharides of hyaluronan (o-HA) promotes wound recovery by accelerating angiogenesis and to study the mechanisms by which o-HA stimulates endothelial cell (EC) proliferation.
Using hyaluronidase digestion, we prepared a mixture of hyaluronan (HA) fragments sizesd 2 to 10 disaccharides units, and studied their effects on EC growth and migration in mimicking wound recovery in vitro. The effects of o-HA on EC growth in vitro were studied by counting cell numbers. The roles of 2 hyaluronan receptors on EC cells, CD44 and RHAMM (Receptor for HA-Mediated Motility), were studied in initiating signaling cascades, using immunoblot assay. Signal transduction was determined by blocking antibodies to CD44 and RHAMM. An in vitro wound healing model was prepared by scratching the cellular layer of cultured EC, and movement of cells into the denuded area was quantified.
o-HA was a strong stimulator to EC proliferation at low concentration 10microg/ml compared with native high molecular weight HA (n-HA) (P < 0.01). Signal transduction may be initiated by o-HA via RHAMM receptor on EC membrane, but not CD44. In the in vitro model, the lesion area was nearly completely recovered when the EC layer was exposed to o-HA 40hrs post-injury, whereas the wound area remained half recovered pretreated with native undegraded large HA and control medium.(P < 0.05 from 24 to 40hrs).
Hyaluronan oligosaccharides may play a role in wound healing by increasing angiogenesis. o-HA-RHAMM binding dependent signal transduction pathway may be important in the regulation of angiogenesis associated with EC proliferation.
确定透明质酸寡糖(o-HA)是否通过加速血管生成来促进伤口愈合,并研究o-HA刺激内皮细胞(EC)增殖的机制。
利用透明质酸酶消化,我们制备了大小为2至10个二糖单位的透明质酸(HA)片段混合物,并在体外模拟伤口愈合过程中研究了它们对EC生长和迁移的影响。通过计数细胞数量研究o-HA对体外EC生长的影响。利用免疫印迹分析研究了EC细胞上的两种透明质酸受体CD44和RHAMM(透明质酸介导的运动受体)在启动信号级联反应中的作用。通过针对CD44和RHAMM的阻断抗体来确定信号转导。通过刮擦培养的EC细胞层制备体外伤口愈合模型,并对细胞向裸露区域的移动进行定量。
与天然高分子量HA(n-HA)相比,o-HA在低浓度10μg/ml时是EC增殖的强刺激剂(P < 0.01)。信号转导可能由o-HA通过EC膜上的RHAMM受体启动,而非CD44。在体外模型中,损伤后40小时当EC层暴露于o-HA时,损伤区域几乎完全恢复,而用天然未降解的大HA和对照培养基预处理时伤口区域仍有一半未恢复(损伤后24至40小时,P < 0.05)。
透明质酸寡糖可能通过增加血管生成在伤口愈合中发挥作用。o-HA-RHAMM结合依赖性信号转导途径可能在与EC增殖相关的血管生成调节中起重要作用。