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Effects of pH on molecular mechanisms of chitosan-integrin interactions and resulting tight-junction disruptions

机译:pH对壳聚糖-整合素相互作用的分子机制及紧密连接破坏的影响

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摘要

Chitosan (CS) is a potential paracellular permeation enhancer for trans-epithelial drug delivery; however, its ability to enhance epithelial permeability in a pH-dependent manner remains unclear. This study was designed to explore the underlying molecular mechanisms with regard to the effect of CS on tight junction (TJ) disruption at different pH environments in Caco-2 cell monolayers. The experimental results revealed that the direct interaction between CS and integrin α Vβ 3 on cell surfaces has a crucial role in CS-induced TJ opening, an indication of receptor activation. The mechanism of action appeared to be the electrostatic interaction between the positively-charged CS and the negatively-charged integrin α Vβ 3. This electrostatic interaction led to the conformation change of integrin α Vβ 3 and its clustering along the cell border, F-actin reorganization, and CLDN4 down-regulation, eventually resulting in the disruption of TJs and an increase in paracellular permeability. The above observations were all in a pH-dependent manner. As pH increased, CS became less positively charged, thereby losing its capability to interact with integrin α Vβ 3 and failing to induce the TJ opening. These consequences might help to better understand the molecular mechanism of TJ opening mediated by CS, thereby facilitating the use of CS for trans-epithelial drug delivery.
机译:壳聚糖(CS)是潜在的跨细胞上皮给药的细胞旁渗透促进剂;然而,其以pH依赖性方式增强上皮通透性的能力仍不清楚。这项研究旨在探讨在Caco-2细胞单层中不同pH环境下CS对紧密连接(TJ)破坏的影响的潜在分子机制。实验结果表明,CS与细胞表面整合素αVβ3之间的直接相互作用在CS诱导的TJ开放中起着至关重要的作用,这是受体激活的指示。作用机理似乎是带正电荷的CS和带负电荷的整联蛋白αVβ3之间的静电相互作用。这种静电相互作用导致整联蛋白αVβ3的构象变化及其沿细胞边界的聚集,F-肌动蛋白。重组和CLDN4下调,最终导致TJ的破坏和旁细胞通透性的增加。以上观察均以pH依赖性方式进行。随着pH的增加,CS的带正电性降低,从而失去了与整联蛋白αVβ3相互作用的能力,并且无法诱导TJ的开放。这些后果可能有助于更好地了解CS介导的TJ开放的分子机制,从而促进CS用于跨上皮药物递送的用途。

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