LPS-induced neutrophilic inflammation and Bcl-2 expression in metaplastic mucous cells

被引:16
作者
Foster, JE
Gott, K
Schuyler, MR
Kozak, W
Tesfaigzi, Y
机构
[1] Lovelace Resp Res Inst, Albuquerque, NM 87108 USA
[2] Univ New Mexico, Sch Med, Albuquerque, NM 87108 USA
[3] Vet Adm Med Ctr, Albuquerque, NM 87108 USA
[4] Med Coll Georgia, Augusta, GA 30912 USA
[5] Nicholas Copernicus Univ, PL-87100 Torun, Poland
关键词
airway epithelium; bezafibrate; apoptosis; lavaged cells; cytokines;
D O I
10.1152/ajplung.00249.2002
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Our previous studies show that Bcl-2, a regulator of apoptosis, may be involved in the reduction of mucous cell metaplasia (MCM) during recovery from inflammatory responses. The present study was to determine whether neutrophilic inflammation mediates Bcl-2 expression in mucous cells. Rats were intratracheally instilled with 50-1,000 mug of LPS. The number of neutrophils recovered by bronchoalveolar lavage (BAL) increased with the dose of LPS, and the percentage of Bcl-2-expressing cells increased with the numbers of neutrophils in the BAL. Depletion of neutrophils did not reduce MCM, but the percentage of Bcl-2-positive cells increased 1.8-fold in neutrophil-depleted compared with controls. Injection of rats with bezafibrate, an inducer of cytochrome P-450, doubled the number of neutrophils in the BAL, decreased MCM twofold compared with vehicle-injected controls, and reduced Bcl-2 expression. Bcl-2 mRNA levels decreased in a tracheal epithelial cell line treated with bezafibrate. These data demonstrate that Bcl-2 expression is independent of the number of neutrophils in the BAL and that bezafibrate may directly reduce Bcl-2 expression in epithelial cells.
引用
收藏
页码:L405 / L414
页数:10
相关论文
共 41 条
[1]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]   16(R)-hydroxyeicosatetraenoic acid, a novel cytochrome P450 product of arachidonic acid, suppresses activation of human polymorphonuclear leukocytes and reduces intracranial pressure in a rabbit model of thromboembolic stroke [J].
Bednar, MM ;
Gross, CE ;
Russell, SR ;
Fuller, SP ;
Ahern, TP ;
Howard, DB ;
Falck, JR ;
Reddy, KM ;
Balazy, M .
NEUROSURGERY, 2000, 47 (06) :1410-1418
[3]   PHENOTYPE AND DIFFERENTIATION POTENTIAL OF A NOVEL RAT TRACHEAL EPITHELIAL-CELL LINE [J].
DOHERTY, MM ;
LIU, JY ;
RANDELL, SH ;
CARTER, CA ;
DAVIS, CW ;
NETTESHEIM, P ;
FERRIOLA, PC .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1995, 12 (04) :385-395
[4]  
El-Zimaity HMT, 1998, ARCH PATHOL LAB MED, V122, P732
[5]  
GIBSON GG, 1991, METHOD ENZYMOL, V206, P353
[6]   Role of α2-macroglobulin in fever and cytokine responses induced by lipopolysaccharide in mice [J].
Gourine, AV ;
Gourine, VN ;
Tesfaigzi, Y ;
Caluwaerts, N ;
Van Leuven, F ;
Kluger, MJ .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2002, 283 (01) :R218-R226
[7]   BCL-2 family members and the mitochondria in apoptosis [J].
Gross, A ;
McDonnell, JM ;
Korsmeyer, SJ .
GENES & DEVELOPMENT, 1999, 13 (15) :1899-1911
[8]   IN-VIVO EFFECTS OF ENDOTOXIN ON DNA-SYNTHESIS IN RAT NASAL EPITHELIUM [J].
HARKEMA, JR ;
HOTCHKISS, JA .
MICROSCOPY RESEARCH AND TECHNIQUE, 1993, 26 (05) :457-465
[9]  
HARKEMA JR, 1992, AM J PATHOL, V141, P307
[10]   INVIVO EFFECTS OF ENDOTOXIN ON NASAL EPITHELIAL MUCOSUBSTANCES - QUANTITATIVE HISTOCHEMISTRY [J].
HARKEMA, JR ;
HOTCHKISS, JA .
EXPERIMENTAL LUNG RESEARCH, 1991, 17 (04) :743-761