Literature DB >> 16918412

Structure and function of the intercellular junctions: barrier of paracellular drug delivery.

Kai Zheng1, Maulik Trivedi, Teruna J Siahaan.   

Abstract

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.

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Year:  2006        PMID: 16918412     DOI: 10.2174/138161206777947722

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  14 in total

1.  Improving the stability of the EC1 domain of E-cadherin by thiol alkylation of the cysteine residue.

Authors:  Maulik Trivedi; Jennifer S Laurence; Todd D Williams; C Russell Middaugh; Teruna J Siahaan
Journal:  Int J Pharm       Date:  2012-04-17       Impact factor: 5.875

2.  Effects of intercellular junction protein expression on intracellular ice formation in mouse insulinoma cells.

Authors:  Adam Z Higgins; Jens O M Karlsson
Journal:  Biophys J       Date:  2013-11-05       Impact factor: 4.033

3.  Modulation of intercellular junctions by cyclic-ADT peptides as a method to reversibly increase blood-brain barrier permeability.

Authors:  Marlyn D Laksitorini; Paul K Kiptoo; Ngoc H On; James A Thliveris; Donald W Miller; Teruna J Siahaan
Journal:  J Pharm Sci       Date:  2015-01-12       Impact factor: 3.534

Review 4.  Pathways and progress in improving drug delivery through the intestinal mucosa and blood-brain barriers.

Authors:  Marlyn Laksitorini; Vivitri D Prasasty; Paul K Kiptoo; Teruna J Siahaan
Journal:  Ther Deliv       Date:  2014-10

5.  Cell-cell junctions: structure and regulation in physiology and pathology.

Authors:  Mir S Adil; S Priya Narayanan; Payaningal R Somanath
Journal:  Tissue Barriers       Date:  2020-12-10

6.  Drug discovery and regulatory considerations for improving in silico and in vitro predictions that use Caco-2 as a surrogate for human intestinal permeability measurements.

Authors:  Caroline A Larregieu; Leslie Z Benet
Journal:  AAPS J       Date:  2013-01-24       Impact factor: 4.009

7.  Probing the interaction between cHAVc3 peptide and the EC1 domain of E-cadherin using NMR and molecular dynamics simulations.

Authors:  Ahmed Alaofi; Elinaz Farokhi; Vivitri D Prasasty; Asokan Anbanandam; Krzysztof Kuczera; Teruna J Siahaan
Journal:  J Biomol Struct Dyn       Date:  2016-04-12

8.  Effect of caveolin-1 on the expression of tight junction-associated proteins in rat glioma-derived microvascular endothelial cells.

Authors:  Yao Li; Li-Bo Liu; Teng Ma; Ping Wang; Yi-Xue Xue
Journal:  Int J Clin Exp Pathol       Date:  2015-10-01

9.  Evaluation of the physical stability of the EC5 domain of E-cadherin: effects of pH, temperature, ionic strength, and disulfide bonds.

Authors:  Kai Zheng; C Russell Middaugh; Teruna J Siahaan
Journal:  J Pharm Sci       Date:  2009-01       Impact factor: 3.534

10.  Characterization of multiple stable conformers of the EC5 domain of E-cadherin and the interaction of EC5 with E-cadherin peptides.

Authors:  Kai Zheng; Jennifer S Laurence; Krzysztof Kuczera; Gennady Verkhivker; C Russell Middaugh; Teruna J Siahaan
Journal:  Chem Biol Drug Des       Date:  2009-06       Impact factor: 2.817

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