Zheng Kai, Trivedi Maulik, Siahaan Teruna J
Department of Pharmaceutical Chemistry, The University of Kansas, Simons Research Laboratories, Lawrence, KS 66047, USA.
Curr Pharm Des. 2006;12(22):2813-24. doi: 10.2174/138161206777947722.
The delivery of large hydrophilic molecules (i.e., peptides and proteins) across biological barriers has been hampered by the presence of tight junctions. This delivery process can be improved by enhancing permeation through intercellular junctions of the intestinal mucosa and blood-brain barriers. This is achieved by modulating the intercellular junctions of these biological barriers. To modulate intercellular junctions, it is necessary to understand the structure and function of the proteins that are involved in these junctions. This review focuses on the structure of intercellular junctions and possible mechanisms of intercellular junction formation. Modulation of protein-protein interactions has been shown to increase the porosity of the paracellular pathway. For example, E-cadherin derived peptides have been shown to enhance the permeation of hydrophilic molecules (i.e., mannitol) in cell culture models of biological barriers.
紧密连接的存在阻碍了大分子亲水性分子(即肽和蛋白质)跨越生物屏障的传递。通过增强其透过肠黏膜和血脑屏障的细胞间连接的渗透作用,可以改善这种传递过程。这可以通过调节这些生物屏障的细胞间连接来实现。为了调节细胞间连接,有必要了解参与这些连接的蛋白质的结构和功能。本综述聚焦于细胞间连接的结构以及细胞间连接形成的可能机制。已表明调节蛋白质 - 蛋白质相互作用可增加细胞旁途径的孔隙率。例如,在生物屏障的细胞培养模型中,E - 钙黏蛋白衍生肽已被证明可增强亲水性分子(即甘露醇)的渗透。