Immunomodulatory and Anti-inflammatory Activity in Vitro and in Vivo of a Novel Antimicrobial Candidate

被引:44
作者
Brunetti, Jlenia [1 ]
Roscia, Giulia [1 ]
Lampronti, Ilaria [2 ]
Gambari, Roberto [2 ]
Quercini, Leila [1 ]
Falciani, Chiara [3 ]
Bracci, Luisa [1 ]
Pini, Alessandro [1 ]
机构
[1] Univ Siena, Dept Med Biotechnol, Via Aldo Moro 2, I-53100 Siena, Italy
[2] Univ Ferrara, Dept Life Sci & Biotechnol, Via Fossato Mortara 74, I-44121 Ferrara, Italy
[3] SetLance Srl, Via Fiorentina 1, I-53100 Siena, Italy
关键词
antimicrobial peptide (AMP); drug discovery; infectious disease; inflammation; LPS; anti-inflammatory agents; HOST-DEFENSE PEPTIDES; CYSTIC-FIBROSIS; BRANCHED PEPTIDES; MECHANISM; RESISTANT; LUNGS;
D O I
10.1074/jbc.M116.750257
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The synthetic antimicrobial peptide SET-M33 has strong activity against bacterial infections caused by Gram-negative bacteria. It is currently in preclinical development as a new drug to treat lung infections caused by Gram-negative bacteria. Here we report its strong anti-inflammatory activity in terms of reduced expression of a number of cytokines, enzymes, and signal transduction factors involved in inflammation triggered by LPS from Pseudomonas aeruginosa, Klebsiella pneumoniae, and Escherichia coli. Sixteen cytokines and other major agents involved in inflammation were analyzed in macrophages and bronchial cells after stimulation with LPS and incubation with SET-M33. The bronchial cells were obtained from a cystic fibrosis patient. A number of these proteins showed up to 100% reduction in expression as measured by RT-PCR, Western blotting, or Luminex technology. LPS neutralization was also demonstrated in vivo by challenging bronchoalveolar lavage of SET-M33-treated mice with LPS, which led to a sharp reduction in TNF- with respect to non-SET-M33-treated animals. We also describe a strong activity of SET-M33 in stimulating cell migration of keratinocytes in wound healing experiments in vitro, demonstrating a powerful immunomodulatory action generally characteristic of molecules taking part in innate immunity.
引用
收藏
页码:25742 / 25748
页数:7
相关论文
共 27 条
[1]   IMMUNOHISTOPATHOLOGIC LOCALIZATION OF PSEUDOMONAS-AERUGINOSA IN LUNGS FROM PATIENTS WITH CYSTIC-FIBROSIS - IMPLICATIONS FOR THE PATHOGENESIS OF PROGRESSIVE LUNG DETERIORATION [J].
BALTIMORE, RS ;
CHRISTIE, CDC ;
SMITH, GJW .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1989, 140 (06) :1650-1661
[2]   Synthetic peptides in the form of dendrimers become resistant to protease activity [J].
Bracci, L ;
Falciani, C ;
Lelli, B ;
Lozzi, L ;
Runci, Y ;
Pini, A ;
De Montis, MG ;
Tagliamonte, A ;
Neri, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (47) :46590-46595
[3]  
Brunetti J., 2016, CURR TOP MED CHEM
[4]   In vitro and in vivo efficacy, toxicity, bio-distribution and resistance selection of a novel antibacterial drug candidate [J].
Brunetti, Jlenia ;
Falciani, Chiara ;
Roscia, Giulia ;
Pollini, Simona ;
Bindi, Stefano ;
Scali, Silvia ;
Arrieta, Unai Cossio ;
Gomez-Vallejo, Vanessa ;
Quercini, Leila ;
Ibba, Elisa ;
Prato, Marco ;
Rossolini, Gian Maria ;
Llop, Jordi ;
Bracci, Luisa ;
Pini, Alessandro .
SCIENTIFIC REPORTS, 2016, 6
[5]   Tumor-selective peptide-carrier delivery of Paclitaxel increases in vivo activity of the drug [J].
Brunetti, Jlenia ;
Pillozzi, Serena ;
Falciani, Chiara ;
Depau, Lorenzo ;
Tenori, Eleonora ;
Scali, Silvia ;
Lozzi, Luisa ;
Pini, Alessandro ;
Arcangeli, Annarosa ;
Menichetti, Stefano ;
Bracci, Luisa .
SCIENTIFIC REPORTS, 2015, 5
[6]   State of the Art: Why do the lungs of patients with cystic fibrosis become infected and why can't they clear the infection? [J].
Chmiel, JF ;
Davis, PB .
RESPIRATORY RESEARCH, 2003, 4 (08)
[7]   Synthesis and biological activity of stable branched neurotensin peptides for tumor targeting [J].
Falciani, Chiara ;
Fabbrini, Monica ;
Pini, Alessandro ;
Lozzi, Luisa ;
Lelli, Barbara ;
Pileri, Silvia ;
Brunetti, Jlenia ;
Bindi, Stefano ;
Scali, Silvia ;
Bracci, Luisa .
MOLECULAR CANCER THERAPEUTICS, 2007, 6 (09) :2441-2448
[8]   Molecular basis of branched peptides resistance to enzyme proteolysis [J].
Falciani, Chiara ;
Lozzi, Luisa ;
Pini, Alessandro ;
Corti, Federico ;
Fabbrini, Monica ;
Bernini, Andrea ;
Lelli, Barbara ;
Niccolai, Neri ;
Bracci, Luisa .
CHEMICAL BIOLOGY & DRUG DESIGN, 2007, 69 (03) :216-221
[9]   Isomerization of an Antimicrobial Peptide Broadens Antimicrobial Spectrum to Gram-Positive Bacterial Pathogens [J].
Falciani, Chiara ;
Lozzi, Luisa ;
Pollini, Simona ;
Luca, Vincenzo ;
Carnicelli, Veronica ;
Brunetti, Jlenia ;
Lelli, Barbara ;
Bindi, Stefano ;
Scali, Silvia ;
Di Giulio, Antonio ;
Rossolini, Gian Maria ;
Mangoni, Maria Luisa ;
Bracci, Luisa ;
Pini, Alessandro .
PLOS ONE, 2012, 7 (10)
[10]   Antimicrobial and host-defense peptides as new anti-infective therapeutic strategies [J].
Hancock, Robert E. W. ;
Sahl, Hans-Georg .
NATURE BIOTECHNOLOGY, 2006, 24 (12) :1551-1557