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1.
Inflammation ; 39(3): 1108-15, 2016 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-27075589

RESUMEN

Small-sized chitin and chitosan microparticles (MPs) reduce allergic inflammation. We examined the capacity of these glycans to stimulate A549 human airway epithelial cells to determine the feasibility of using of these glycans as allergic therapeutic modality. A549 cells were treated with MPs and then expressions levels of chitinase domain-containing 1 (CHID1) and chitinase 3-like 1 (CHI3L1) genes were determined by quantitative real-time PCR. IL-6 production was measured by ELISA. Chitin MPs resulted in upregulation of CHI3L1 expression by 35.7-fold while mRNA expression did not change with chitosan MPs. Compared to the untreated group, production of IL-6 was significantly decreased in the chitosan MPs-treated group, but chitin MPs treatment cause elevation of IL-6 level. This study demonstrates that chitin potently induces CHI3L1 expression, but chitosan is relatively inert. This effect and inhibition of pro-inflammatory cytokine (IL-6) suggest that chitosan MPs may possess more potential for therapeutic uses in human airway allergic inflammation.


Asunto(s)
Quitina/farmacología , Quitosano/farmacología , Citocinas/biosíntesis , Células Epiteliales/efectos de los fármacos , Expresión Génica/efectos de los fármacos , Células A549 , Asma/patología , Quitina/administración & dosificación , Proteína 1 Similar a Quitinasa-3/biosíntesis , Proteína 1 Similar a Quitinasa-3/genética , Quitinasas , Quitosano/administración & dosificación , Citocinas/efectos de los fármacos , Sistemas de Liberación de Medicamentos , Células Epiteliales/metabolismo , Células Epiteliales/patología , Humanos , Inflamación/tratamiento farmacológico , Inflamación/metabolismo , Interleucina-6/biosíntesis , Interleucina-6/genética , Sistema Respiratorio/patología
2.
Chem Biol Drug Des ; 84(2): 242-52, 2014 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-24581146

RESUMEN

LAH4 is an antimicrobial peptide that is believed to possess both antibiotic and DNA delivery capabilities. It is one of a number of membrane-active peptides that show increased affinity toward anionic lipids. Herein, we have performed molecular dynamics simulations to compare LAH4 effects on anionic palmitoyl-oleoyl-phosphatidylglycerol bilayer, which approximate a prokaryotic membrane environment and zwitterionic palmitoyl-oleoyl-phosphatidylcholine bilayer, which approximate a eukaryotic membrane environment. One particular interest in this work is to study how different kinds of lipid bilayers respond to the attraction of LAH4. Remarkably, our data have shown that the depth of peptide penetration strongly depends on membrane composition and pH. At acidic pH, LAH4 has exhibited a high tendency to interact strongly with and be adsorbed on anionic membrane. We have also shown that electrostatic interactions between His11 and the phosphor atoms of bilayers should have a significant impact on the penetration of LAH4. These results provide insights into the interactions of LAH4 and lipid bilayers at the atomic level, which is useful to understand cell selectivity and mechanism of the peptide action.


Asunto(s)
Membrana Dobles de Lípidos/metabolismo , Péptidos/metabolismo , Fosfatidilcolinas/metabolismo , Fosfatidilgliceroles/metabolismo , Péptidos Catiónicos Antimicrobianos , Concentración de Iones de Hidrógeno , Simulación de Dinámica Molecular
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