Expression of transforming growth factor beta (TGF-b1) by human preterm lung inflammatory cells

被引:18
|
作者
Kwong, K. Y. [1 ]
Niang, S.
Literat, A.
Zhu, N. L.
Ramanathan, R.
Jones, C. A.
Minoo, P.
机构
[1] Los Angeles Cty & Univ So Calif Med Ctr, Dept Pediat, Div Allergy Immunol, Los Angeles, CA 90033 USA
[2] Los Angeles Cty & Univ So Calif Med Ctr, Dept Pediat, Div Neonatol, Los Angeles, CA 90033 USA
[3] Los Angeles Cty & Univ So Calif Med Ctr, Dept Pediat, Div Basic Res, Los Angeles, CA 90033 USA
关键词
transforming growth factor beta 1; premature; inflammation; lung; bronchopulmonary dysplasia; lipopolysaccharide;
D O I
10.1016/j.lfs.2006.07.040
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Using a previously published model of human BPD this study examines whether preterm lung inflammatory cells produce transforming growth factor beta 1 (TGF-beta 1), a cytokine pivotal in pathogenesis of bronchopulmonary dysplasia (BPD), and whether TGF-beta 1 expression is regulated by inflammation. Lung inflammatory cells (neutrophils and macrophages) recovered in the broncho-alveolar (BAL) fluid of premature infants intubated for respiratory distress after birth expressed TGF-b1 mRNA and protein. Total and bioactive TGF-beta 1 were abundantly found in the BAL fluid of the same infants. In cell culture stimulation by lipopolysaccharide (LPS) did not result in any further expression of total or bioactive TGF-beta 1 I by neonatal lung inflammatory cells over constitutive concentrations. In conclusion, lung inflammatory cells from premature infants are a source of TGF-beta 1 but LPS does not regulate TGF-b1 production in these cells. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:2349 / 2356
页数:8
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