Cathelicidin-deficient mice exhibit increased survival and upregulation of key inflammatory response genes following cecal ligation and puncture
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Citações na Scopus
17
Tipo de produção
article
Data de publicação
2017
Título da Revista
ISSN da Revista
Título do Volume
Editora
SPRINGER
Autores
SEVERINO, Patricia
SILVA, Elisangela de Paula
NIZET, Victor
Citação
JOURNAL OF MOLECULAR MEDICINE-JMM, v.95, n.9, p.995-1003, 2017
Resumo
Antimicrobial peptides possess a myriad of molecular properties including bacterial killing and the regulation of many aspects of innate immunity. Cathelicidins are a group of antimicrobial peptides widely investigated by the scientific community. Many studies have focused on the bactericidal and pro-inflammatory roles of cathelicidins. Because the role of endogenous cathelicidin expression remains obscure in deep-seated systemic infections, we induced sepsis in cathelicidin knockout and wild-type (WT) mice by cecal ligation and puncture, performing transcriptome screening by DNA micro-array in conjunction with other immunologic assays. Cathelicidin-deficient mice showed increased survival compared to WT mice in this established experimental model of polymicrobial sepsis, in association with upregulation of certain key inflammatory response genes. Therefore, cathelicidins can exert both pro- and anti-inflammatory activities depending on the disease and cellular context.
Palavras-chave
Sepsis, Cathelicidin, Inflammation, Gene expression
Referências
- Audrain B, 2013, APPL ENVIRON MICROB, V79, P7770, DOI 10.1128/AEM.02593-13
- Barbeiro DF, 2013, MICROBES INFECT, V15, P342, DOI 10.1016/j.micinf.2013.01.001
- Beaumont PE, 2014, PLOS ONE, V9, DOI 10.1371/journal.pone.0099029
- Chromek M, 2006, NAT MED, V12, P636, DOI 10.1038/nm1407
- Chromek M, 2012, PLOS ONE, V7, DOI 10.1371/journal.pone.0046476
- Ciornei CD, 2005, ANTIMICROB AGENTS CH, V49, P2845, DOI 10.1128/AAC.49.7.2845-2850.2005
- Cirioni O, 2006, ANTIMICROB AGENTS CH, V50, P1672, DOI 10.1128/AAC.50.5.1672-1679.2006
- Coffelt SB, 2009, MOL CANCER RES, V7, P907, DOI 10.1158/1541-7786.MCR-08-0326
- Cole JN, 2016, MICROBIOL SPECTR, V4, DOI 10.1128/microbiolspec.VMBF-0006-2015
- Coorens M, 2017, SCI REP-UK, V7, DOI 10.1038/srep40874
- da Silva FP, 2017, IMMUNOL LETT, V182, P57, DOI 10.1016/j.imlet.2017.01.004
- da Silva FP, 2013, TISSUE CELL, V45, P318, DOI 10.1016/j.tice.2013.04.003
- da Silva FP, 2012, PEPTIDES, V36, P308, DOI 10.1016/j.peptides.2012.05.014
- da Silva FP, 2009, IMMUNOL CELL BIOL, V87, P496, DOI 10.1038/icb.2009.19
- Danka ES, 2015, J INFECT DIS, V211, P1164, DOI 10.1093/infdis/jiu577
- Devitt A, 1998, NATURE, V392, P505
- Durr UHN, 2006, BBA-BIOMEMBRANES, V1758, P1408, DOI 10.1016/j.bbamem.2006.03.030
- Gallo RL, 1997, J BIOL CHEM, V272, P13088, DOI 10.1074/jbc.272.20.13088
- Gudmundsson GH, 1996, EUR J BIOCHEM, V238, P325, DOI 10.1111/j.1432-1033.1996.0325z.x
- Iimura M, 2005, J IMMUNOL, V174, P4901
- Jeng L, 2009, J TRANSL MED, V7, DOI 10.1186/1479-5876-7-28
- Kingsley SMK, 2016, CURR INFECT DIS REP, V18, DOI 10.1007/s11908-016-0535-8
- LARRICK JW, 1995, INFECT IMMUN, V63, P1291
- Lipovsky MM, 1997, CLIN IMMUNOL IMMUNOP, V84, P208, DOI 10.1006/clin.1997.4381
- Livak KJ, 2001, METHODS, V25, P402, DOI 10.1006/meth.2001.1262
- Martin L, 2015, FRONT IMMUNOL, V6, DOI 10.3389/fimmu.2015.00404
- Mookherjee N, 2007, EXPERT OPIN THER TAR, V11, P993, DOI 10.1517/14728222.11.8.993
- Munoz M, 2016, J CANCER, V7, P2341, DOI 10.7150/jca.16947
- Muro M, 1997, INFECT IMMUN, V65, P1147
- Nagaoka I, 2012, ISRN MICROBIOL, V2012
- Nakagawa Y, 2015, J IMMUNOL, V194, P1274, DOI 10.4049/jimmunol.1402388
- Niyonsaba F, 2002, IMMUNOLOGY, V106, P20, DOI 10.1046/j.1365-2567.2002.01398.x
- Nizet V, 2001, NATURE, V414, P454, DOI 10.1038/35106587
- Oren Z, 1999, BIOCHEM J, V341, P501, DOI 10.1042/0264-6021:3410501
- PETERSON PK, 1995, INFECT IMMUN, V63, P1598
- Ramanathan B, 2002, MICROBES INFECT, V4, P361, DOI 10.1016/S1286-4579(02)01549-6
- Ries M, 2013, J LEUKOCYTE BIOL, V94, P123, DOI 10.1189/jlb.0612278
- Salzer S, 2014, J DERMATOL SCI, V76, P173, DOI 10.1016/j.jdermsci.2014.09.002
- Thomassin Jenny-Lee, 2012, Gut Microbes, V3, P556, DOI 10.4161/gmic.21656
- Tjabringa GS, 2006, INT ARCH ALLERGY IMM, V140, P103, DOI 10.1159/000092305
- von Kockritz-Blickwede M, 2008, BLOOD, V111, P3070, DOI 10.1182/blood-2007-07-104018
- Wan M, 2014, J LEUKOCYTE BIOL, V95, P971, DOI 10.1189/jlb.0513304
- Wewers MD, 2009, PURINERG SIGNAL, V5, P189, DOI 10.1007/s11302-009-9131-9
- WICHTERMAN KA, 1980, J SURG RES, V29, P189, DOI 10.1016/0022-4804(80)90037-2
- Yin J, 2010, INVEST OPHTH VIS SCI, V51, P1891, DOI 10.1167/iovs.09-3904
- Zaiou M, 2002, J MOL MED-JMM, V80, P549, DOI 10.1007/s00109-002-0350-6