Rotavirus-Like Particles: A Novel Nanocarrier for the Gut

被引:17
|
作者
Cortes-Perez, Naima G. [1 ,2 ,3 ]
Sapin, Catherine [1 ,2 ]
Jaffrelo, Loic [1 ,2 ]
Daou, Sabine [1 ,2 ]
Grill, Jean Pierre [1 ,2 ]
Langella, Philippe [3 ]
Seksik, Philippe [1 ,2 ,4 ]
Beaugerie, Laurent [1 ,2 ,4 ]
Chwetzoff, Serge [1 ,2 ,5 ]
Trugnan, Germain [1 ,2 ]
机构
[1] Univ Paris 06, UPMC, UMRS Traf Membranaire & Signalisat Cellules Epith, F-75012 Paris, France
[2] CHU St Antoine, INSERM, UMRS Traf Membranaire & Signalisat Cellules Epith, F-75012 Paris, France
[3] Unite INRA Ecol & Physiol Syst Digestif, Jouy En Josas, France
[4] Hop St Antoine, AP HP, Serv Gastroenterol & Nutr, F-75012 Paris, France
[5] INRA, Unite Virol & Immunol Mol, UR 089, F-78352 Jouy En Josas, France
关键词
LACTIC-ACID BACTERIA; SPIKE PROTEIN; ALPHA-2-BETA-1; INTEGRIN; CELLS; VIRUS; INFECTIVITY; MEMBRANE; MODEL; VP4; IMMUNIZATION;
D O I
10.1155/2010/317545
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The delivery of bioactive molecules directly to damaged tissues represents a technological challenge. We propose here a new system based on virus-like particles (VLP) from rotavirus, with a marked tropism for the gut to deliver bio-active molecules to intestinal cells. For this, nonreplicative VLP nanoparticles were constructed using a baculovirus expression system and used to deliver an exogenous biomolecule, the green fluorescent protein (GFP), into either MA104 cells or intestinal cells from healthy and 2,4,6-trinitrobenzene sulfonic acid (TNBS)-treated mice. Our results show that expression of rotavirus capsid proteins in baculovirus led to the auto assembly of VLP that display similar properties to rotavirus. In vitro experiments showed that VLP were able to enter into MA104 cells and deliver the reporter protein. Intragastric administration of fluorescent VLP in healthy and TNBS-treated mice resulted in the detection of GFP and viral proteins in intestinal samples. Our results demonstrate an efficient entry of non-replicative rotavirus VLP into the epithelial cell line MA104 and provide the first in vivo evidence of the potential of these nanoparticles as a promising safe candidate for drug delivery to intestinal cells. Copyright (C) 2010 Naima G. Cortes-Perez et al.
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页数:10
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