β-defensin gene expression during the course of experimental tuberculosis infection

被引:72
作者
Rivas-Santiago, Bruno
Sada, Eduardo
Tsutsumi, Victor
Aguilar-Leon, Diana
Contreras, Juan Leon
Hernandez-Pando, Rogelio
机构
[1] Inst Nacl Nutr Salvador Zubiran, Inst Med Sci, Expt Pathol Sect, Dept Pathol, Mexico City 14000, DF, Mexico
[2] Natl Inst Resp Dis, Dept Microbiol Res, Mexico City 14000, DF, Mexico
[3] Natl Polytech Inst, Ctr Res & Adv Studies, Dept Expt Pathol, Mexico City 14000, DF, Mexico
关键词
D O I
10.1086/506454
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The kinetics of gene expression and the cellular source of murine beta-defensin-3 (mBD3) and murine beta-defensin-4 (mBD4) were determined in mouse models of progressive pulmonary tuberculosis and latent infection induced by high or low infecting doses, respectively. During progressive disease, there was an initial rapid expression of both defensins by respiratory epithelial cells that correlated with temporary control of bacillary proliferation, but expression decreased during the later progressive phase of the disease. In latent infection, both defensins were expressed continuously, but they were suppressed after reactivation of the disease. Thus, mycobacterial infection induces the expression of mBD3 and mBD4, and both might participate in the control of mycobacterial growth.
引用
收藏
页码:697 / 701
页数:5
相关论文
共 15 条
[1]   Immunological and pathological comparative analysis between experimental latent tuberculous infection and progressive pulmonary tuberculosis [J].
Arriaga, AK ;
Orozco, EH ;
Aguilar, LD ;
Rook, GAW ;
Pando, RH .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2002, 128 (02) :229-237
[2]   Elevated levels of α-defensins in plasma and BAL fluid of patients with active pulmonary tuberculosis [J].
Ashitani, J ;
Mukae, H ;
Hiratsuka, T ;
Nakazato, M ;
Kumamoto, K ;
Matsukura, S .
CHEST, 2002, 121 (02) :519-526
[3]   Demonstration of spread by Mycobacterium tuberculosis bacilli in A549 epithelial cell monolayers [J].
Castro-Garza, J ;
King, CH ;
Swords, WE ;
Quinn, FD .
FEMS MICROBIOLOGY LETTERS, 2002, 212 (02) :145-149
[4]  
Flynn JL, 1998, J IMMUNOL, V160, P1796
[5]   Defensins: Antimicrobial peptides of innate immunity [J].
Ganz, T .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (09) :710-720
[6]   Human β-defensin 4:: a novel inducible peptide with a specific salt-sensitive spectrum of antimicrobial activity [J].
García, JRC ;
Krause, A ;
Schulz, S ;
Rodríguez-Jiménez, FJ ;
Klüver, E ;
Adermann, K ;
Forssmann, U ;
Frimpong-Boateng, A ;
Bals, R ;
Forssmann, WG .
FASEB JOURNAL, 2001, 15 (08) :1819-+
[7]   Human beta-defensin-1 is a salt-sensitive antibiotic in lung that is inactivated in cystic fibrosis [J].
Goldman, MJ ;
Anderson, GM ;
Stolzenberg, ED ;
Kari, UP ;
Zasloff, M ;
Wilson, JM .
CELL, 1997, 88 (04) :553-560
[8]   Isolation and characterization of human β-defensin-3, a novel human inducible peptide antibiotic [J].
Harder, J ;
Bartels, J ;
Christophers, E ;
Schröder, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (08) :5707-5713
[9]  
HernandezPando R, 1996, IMMUNOLOGY, V89, P26
[10]   Mechanisms of latency in Mycobacterium tuberculosis [J].
Parrish, NM ;
Dick, JD ;
Bishai, WR .
TRENDS IN MICROBIOLOGY, 1998, 6 (03) :107-112