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The Role of Hyaluronic Acid in Cartilage Boundary Lubrication

机译:透明质酸在软骨边界润滑中的作用

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摘要

Hydration lubrication has emerged as a new paradigm for lubrication in aqueous and biological media, accounting especially for the extremely low friction (friction coefficients down to 0.001) of articular cartilage lubrication in joints. Among the ensemble of molecules acting in the joint, phosphatidylcholine (PC) lipids have been proposed as the key molecules forming, in a complex with other molecules including hyaluronic acid (HA), a robust layer on the outer surface of the cartilage. HA, ubiquitous in synovial joints, is not in itself a good boundary lubricant, but binds the PC lipids at the cartilage surface; these, in turn, massively reduce the friction via hydration lubrication at their exposed, highly hydrated phosphocholine headgroups. An important unresolved issue in this scenario is why the free HA molecules in the synovial fluid do not suppress the lubricity by adsorbing simultaneously to the opposing lipid layers, i.e., forming an adhesive, dissipative bridge between them, as they slide past each other during joint articulation. To address this question, we directly examined the friction between two hydrogenated soy PC (HSPC) lipid layers (in the form of liposomes) immersed in HA solution or two palmitoyl–oleoyl PC (POPC) lipid layers across HA–POPC solution using a surface force balance (SFB). The results show, clearly and surprisingly, that HA addition does not affect the outstanding lubrication provided by the PC lipid layers. A possible mechanism indicated by our data that may account for this is that multiple lipid layers form on each cartilage surface, so that the slip plane may move from the midplane between the opposing surfaces, which is bridged by the HA, to an HA-free interface within a multilayer, where hydration lubrication is freely active. Another possibility suggested by our model experiments is that lipids in synovial fluid may complex with HA, thereby inhibiting the HA molecules from adhering to the lipids on the cartilage surfaces.
机译:水合润滑作为水性和生物介质中润滑的新范式,特别是对于关节关节上的关节软骨润滑的极低摩擦(摩擦系数下降至0.001)。在作用于关节的分子的集合中,已经提出了磷脂酰胆碱(PC)脂质作为形成的关键分子,其与包括透明质酸(HA)的其他分子的复合物中,在软骨外表面上的鲁棒层。 HA,在滑膜接头中无处不在,本身并不是一种良好的边界润滑剂,但在软骨表面结合PC脂质;反过来,这些通过在暴露的高度水化的磷化物头组中通过水化润滑大量减少摩擦。这种情况下的重要未解决的问题是加工流体中的游离HA分子不会通过同时吸附到相对的脂质层,即形成粘合剂,在它们之间形成粘合剂的耗散桥,因为它们在关节期间彼此滑动关节。为了解决这个问题,我们直接检查了两个氢化大豆(HSPC)脂质层(以脂质体形式)之间的摩擦浸入HA溶液或两种Palmitoyl-Oleoyl PC(POPC)脂质层,使用表面横跨HA-POPC溶液力平衡(SFB)。结果明确且令人惊讶地表明,HA添加不会影响PC脂质层提供的出色润滑。我们的数据指示的可能机制可以解释这一点是在每个软骨表面上形成多种脂质层,使得滑动平面可以从相对表面之间的中间平面移动,该相对表面之间由HA桥接到无HA。多层内部的界面,水合润滑自由活跃。我们的模型实验建议的另一种可能性是滑膜流体中的脂质可以与HA复合,从而抑制HA分子粘附在软骨表面上的脂质。

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