Oral Bifidobacterium longum expressing alpha-melanocyte-stimulating hormone to fight experimental colitis

被引:20
作者
Wei, Pijin [1 ]
Yang, Yan [1 ]
Liu, Zhaobing [1 ]
Huang, Junli [1 ]
Gong, Yahui [1 ]
Sun, Hanxiao [1 ]
机构
[1] Jinan Univ, Inst Genom Med Res, Coll Pharm, Guangzhou 510632, Guangdong, Peoples R China
关键词
alpha-MSH; Bifidobacterium; colitis; peptide delivery; INFLAMMATORY-BOWEL-DISEASE; IN-VITRO; FURIN; MSH; PEPTIDES; SYSTEM;
D O I
10.3109/10717544.2015.1122672
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The oral delivery of peptides is a highly attractive treatment approach. However, the harsh environment of the gastrointestinal tract limits its application. Here, we utilize Bifidobacterium as a delivery system to orally deliver a potent anti-inflammatory but short duration peptide alpha-melanocyte-stimulating hormone (alpha-MSH) against experimental colitis. The aim of our study was to facilitate the efficient oral delivery of alpha-MSH. We designed a vector of pBDMSH and used it to construct a Bifidobacterium longum expressing alpha-MSH. We then determined the bioactivity of recombinant Bifidobacterium in lipopolysaccharide-induced inflammatory models of HT-29 cells. Finally, we used Bifidobacterium expressing alpha-MSH against dextran sulfate sodium (DSS)-induced ulcerative colitis mice. Results based on the myeloperoxidase activity, the levels of inflammatory cytokines TNF-alpha, IL-1 beta, IL-6, and IL-10 and the histological injury of colon tissue reveal recombinant Bifidobacterium was efficient in attenuating DSS-induced ulcerative colitis, suggesting an alternative way to use Bifidobacterium as a delivery system to deliver alpha-MSH for DSS-induced ulcerative colitis therapy.
引用
收藏
页码:2058 / 2064
页数:7
相关论文
共 30 条
[1]  
[Anonymous], J MICROBIOLOGY BIOTE
[2]  
AYOUBI TAY, 1994, J BIOL CHEM, V269, P9298
[3]   α-melanocyte-stimulating hormone and related tripeptides:: Biochemistry, antiinflammatory and protective effects in vitro and in vivo, and future perspectives for the treatment of immune-mediated inflammatory diseases [J].
Brzoska, Thomas ;
Luger, Thomas A. ;
Maaser, Christian ;
Abels, Christoph ;
Boehm, Markus .
ENDOCRINE REVIEWS, 2008, 29 (05) :581-602
[4]  
Brzoska T, 2010, ADV EXP MED BIOL, V681, P107, DOI 10.1007/978-1-4419-6354-3_8
[5]  
Chin J, 2012, DRUG DISCOV TODAY TE, V9, pe171
[6]   A review of advanced oral drug delivery technologies facilitating the protection and absorption of protein and peptide molecules [J].
Choonara, Bibi F. ;
Choonara, Yahya E. ;
Kumar, Pradeep ;
Bijukumar, Divya ;
du Toit, Lisa C. ;
Pillay, Viness .
BIOTECHNOLOGY ADVANCES, 2014, 32 (07) :1269-1282
[7]   A novel binary expression vector for production of human IL-10 in Escherichia coli and Bifidobacterium longum [J].
Escogido, M. L. Reyes ;
Rodriguez, A. De Leon ;
de la Rosa, A. P. Barba .
BIOTECHNOLOGY LETTERS, 2007, 29 (08) :1249-1253
[8]   Salvinorin A has antiinflammatory and antinociceptive effects in experimental models of colitis in mice mediated by KOR and CB1 receptors [J].
Fichna, Jakub ;
Dicay, Michael ;
Lewellyn, Kevin ;
Janecka, Anna ;
Zjawiony, Jordan K. ;
MacNaughton, Wallace K. ;
Storr, Martin A. .
INFLAMMATORY BOWEL DISEASES, 2012, 18 (06) :1137-1145
[9]   Bifidobacterium longum as an oral delivery system of endostatin for gene therapy on solid liver cancer [J].
Fu, GF ;
Li, X ;
Hou, YY ;
Fan, YR ;
Liu, WH ;
Xu, GX .
CANCER GENE THERAPY, 2005, 12 (02) :133-140
[10]   Mesenteric adipose tissue alterations resulting from experimental, reactivated colitis [J].
Gambero, Alessandro ;
Marostica, Marta ;
Saad, Mario Jose Abdollo ;
Pedrazzoli, Jose, Jr. .
INFLAMMATORY BOWEL DISEASES, 2007, 13 (11) :1357-1364