Pro-Inflammatory Cytokine Responses of A549 Epithelial Cells to Antimicrobial Peptide Brevinin-2R

被引:11
作者
Asoodeh, Ahmad [1 ,2 ]
Haghparast, Alireza [2 ,3 ]
Kashef, Reyhane [1 ]
Chamani, Jamshidkhan [4 ]
机构
[1] Ferdowsi Univ Mashhad, Dept Chem, Fac Sci, Mashhad, Iran
[2] Ferdowsi Univ Mashhad, Inst Biotechnol, Mashhad, Iran
[3] Ferdowsi Univ Mashhad, Dept Pathobiol, Fac Vet Med, Mashhad, Iran
[4] Islamic Azad Univ, Dept Biol, Fac Sci, Mashhad Branch, Mashhad, Iran
基金
美国国家科学基金会;
关键词
Brevinin-2R; Pro-inflammatory cytokine; Inflammation; MTT assay; Real time PCR; INNATE IMMUNITY; CATHELICIDIN; LL-37; DEFENSINS; RECEPTOR; GROWTH;
D O I
10.1007/s10989-012-9328-6
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
Brevinin-2R is an antimicrobial peptide which has been isolated from the skin of the frog Rana ridibunda. The purpose of the present study was to examine the cellular cytotoxicity and inflammatory effects of brevinin-2R (B2R) on human lung epithelial adenocarcinoma cell line A549. The effects of different concentrations (5, 10, and 20 mu g/ml) of B2R on the expression levels of pro-inflammatory cytokines such as IL-1 beta, and IL-8 in A549 cells were evaluated by semi-quantitative RT-PCR and real-time PCR assays in a dose- and time-dependent manner. Based on the results of MTT assay, B2R showed a moderate cytotoxicity effect in a dose-dependent manner up to 20 % suppression of the cell growth. Moreover, gene expression results demonstrated that B2R up-regulates the IL-1 beta and IL-8 expression levels in A549 cells in a dose- and time-dependent manner. Our results suggested that brevinin-2R antimicrobial peptide has potentially a regulatory effect on triggering the inflammatory processes.
引用
收藏
页码:157 / 162
页数:6
相关论文
共 29 条
[1]   Antimicrobial human beta-defensin-2 stimulates migration, proliferation and tube formation of human umbilical vein endothelial cells [J].
Baroni, Adone ;
Donnarumma, Giovanna ;
Paoletti, Iole ;
Longanesi-Cattani, Immacolata ;
Bifulco, Katia ;
Tufano, Maria Antonietta ;
Carriero, Maria Vincenza .
PEPTIDES, 2009, 30 (02) :267-272
[2]   The human cationic peptide LL-37 induces activation of the extracellular signal-regulated kinase and p38 kinase pathways in primary human monocytes [J].
Bowdish, DME ;
Davidson, DJ ;
Speert, DP ;
Hancock, REW .
JOURNAL OF IMMUNOLOGY, 2004, 172 (06) :3758-3765
[3]   Antimicrobial peptide rCRAMP induced glial cell activation through P2Y receptor signalling pathways [J].
Brandenburg, Lars-Ove ;
Jansen, Sandra ;
Wruck, Christoph J. ;
Lucius, Ralph ;
Pufe, Thomas .
MOLECULAR IMMUNOLOGY, 2010, 47 (10) :1905-1913
[4]   Anti-microbial peptides:: from invertebrates to vertebrates [J].
Bulet, P ;
Stöcklin, R ;
Menin, L .
IMMUNOLOGICAL REVIEWS, 2004, 198 :169-184
[5]  
Eckmann Lars, 1995, Trends in Microbiology, V3, P118, DOI 10.1016/S0966-842X(00)88894-0
[6]   A novel P2X7 receptor activator, the human cathelicidin-derived peptide LL37, induces IL-1β processing and release [J].
Elssner, A ;
Duncan, M ;
Gavrilin, M ;
Wewers, MD .
JOURNAL OF IMMUNOLOGY, 2004, 172 (08) :4987-4994
[7]   Brevinin-2R1 semi-selectively kills cancer cells by a distinct mechanism, which involves the lysosomal-mitochondrial death pathway [J].
Ghavami, Saeid ;
Asoodeh, Ahmad ;
Klonisch, Thomas ;
Halayko, Andrew J. ;
Kadkhoda, Kamran ;
Kroczak, Tadeusz J. ;
Gibson, Spencer B. ;
Booy, Evan P. ;
Naderi-Manesh, Hossein ;
Los, Marek .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2008, 12 (03) :1005-1022
[8]   The role of cationic antimicrobial peptides in innate host defences [J].
Hancock, REW ;
Diamond, G .
TRENDS IN MICROBIOLOGY, 2000, 8 (09) :402-410
[9]   The cathelicidin anti-microbial peptide LL-37 is involved in re-epithelialization of human skin wounds and is lacking in chronic ulcer epithelium [J].
Heilborn, JD ;
Nilsson, MF ;
Kratz, G ;
Weber, G ;
Sorensen, O ;
Borregaard, N ;
Ståhle-Bäckdahl, M .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 120 (03) :379-389
[10]   Human neutrophil peptides induce interleukin-8 production through the P2Y6 signaling pathway [J].
Khine, AA ;
Del Sorbo, L ;
Vaschetto, R ;
Voglis, S ;
Tullis, E ;
Slutsky, AS ;
Downey, GP ;
Zhang, HB .
BLOOD, 2006, 107 (07) :2936-2942