Dexamethasone can stimulate G1-S phase transition in human airway fibroblasts in asthma

被引:19
作者
Fouty, B
Moss, T
Solodushko, V
Kraft, M
机构
[1] Univ S Alabama, Sch Med, Ctr Lung Biol, Mobile, AL 36688 USA
[2] Univ S Alabama, Sch Med, Div Pulm & Crit Care Med, Mobile, AL 36688 USA
[3] Univ Colorado, Hlth Sci Ctr, Boulder, CO 80309 USA
[4] Natl Jewish Med & Res Ctr, Dept Med, Denver, CO USA
[5] Duke Univ, Med Ctr, Dept Med, Durham, NC 27706 USA
[6] Duke Univ, Med Ctr, Duke Asthma Allergy & Airway Ctr, Durham, NC 27706 USA
关键词
asthma; cell cycle; dexamethasone; fibroblast;
D O I
10.1183/09031936.06.00078605
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Corticosteroids are the first line of therapy for asthma. Whether they alter the progression of airway remodelling in asthma is, as yet, unknown. To determine whether corticosteroids could alter the fibroblast cell cycle the current authors studied the effect of dexamethasone on cultured airway fibroblasts obtained from nine mild-to-moderate, steroid-naive asthmatics (forced expiratory volume in one second 78 +/- 4% predicted), and seven normal controls. Fibroblasts were cultured from endobronchial biopsies obtained via bronchoscopy. Cells were exposed to dexamethasone (10(-9)10(-7)M) and studied at 72 h to determine differences in progression through the cell cycle. In asthmatic fibroblasts, dexamethasone, at concentrations of 10(-8)M and 10(-7)M, nearly doubled the number of cells in the S phase (17.8 +/- 3.0% and 18.4 +/- 3.1%, respectively) compared with untreated fibroblasts (10.3 +/- 1.4%). There was no significant effect in normal control fibroblasts. Dexamethasone induced hyperphosphorylation of the tumour suppressor, retinoblastoma (RB) in asthmatic fibroblasts; fibroblasts from normal controls had significantly less hyperphosphorylation of RB. No difference in protein expression of the CCAAT/enhancer binding protein a between the two groups was detected. This study suggests that dexamethasone can stimulate G1-S phase cell cycle transition in human airway fibroblasts obtained from asthmatics. Whether this leads to enhanced airway remodelling in some individuals remains to be determined.
引用
收藏
页码:1160 / 1167
页数:8
相关论文
共 33 条
[1]   MYOFIBROBLASTS AND SUBEPITHELIAL FIBROSIS IN BRONCHIAL-ASTHMA [J].
BREWSTER, CEP ;
HOWARTH, PH ;
DJUKANOVIC, R ;
WILSON, J ;
HOLGATE, ST ;
ROCHE, WR .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1990, 3 (05) :507-511
[2]   Airway remodeling and repair [J].
Busse, W ;
Elias, J ;
Sheppard, D ;
Banks-Schlegel, S .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 160 (03) :1035-1042
[3]  
Dubé J, 1998, LAB INVEST, V78, P297
[4]   CYTOKINE NETWORKS IN THE REGULATION OF INFLAMMATION AND FIBROSIS IN THE LUNG [J].
ELIAS, JA ;
FREUNDLICH, B ;
KERN, JA ;
ROSENBLOOM, J .
CHEST, 1990, 97 (06) :1439-1445
[5]   Distribution of inhaled fluticasone propionate between human lung tissue and serum in vivo [J].
Esmailpour, N ;
Hogger, P ;
Rabe, KF ;
Heitmann, U ;
Nakashima, M ;
Rohdewald, P .
EUROPEAN RESPIRATORY JOURNAL, 1997, 10 (07) :1496-1499
[6]   Glucocorticoids inhibit proliferation, cyclin D1 expression, and retinoblastoma protein phosphorylation, but not activity of the extracellular-regulated kinases in human cultured airway smooth muscle [J].
Fernandes, D ;
Guida, E ;
Koutsoubos, V ;
Harris, T ;
Vadiveloo, P ;
Wilson, JW ;
Stewart, AG .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1999, 21 (01) :77-88
[7]   Mevastatin can cause G1 arrest and induce apoptosis in pulmonary artery smooth muscle cells through a p27Kip1-independent pathway [J].
Fouty, BW ;
Rodman, DM .
CIRCULATION RESEARCH, 2003, 92 (05) :501-509
[8]   Inhibition of intimal thickening after balloon angioplasty in porcine coronary arteries by targeting regulators of the cell cycle [J].
Gallo, R ;
Padurean, A ;
Jayaraman, T ;
Marx, S ;
Rogue, M ;
Adelman, S ;
Chesebro, J ;
Fallon, J ;
Fuster, V ;
Marks, A ;
Badimon, JJ .
CIRCULATION, 1999, 99 (16) :2164-2170
[9]  
GAULDIE J, 1992, AM REV RESPIR DIS, V145, P14
[10]   Inhaled corticosteroids decrease subepithelial collagen deposition by modulation of the balance between matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 expression in asthma [J].
Hoshino, M ;
Takahashi, M ;
Takai, Y ;
Sim, J .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1999, 104 (02) :356-363