首页> 外文期刊>Developmental and Comparative Immunology: Ontogeny, Phylogeny, Aging: The Official Journal of the International Society of Developmental and Comparative Immunology >Expression of select immune genes (surfactant proteins A and D, sheep beta defensin 1, and toll-like receptor 4) by respiratory epithelia is developmentally regulated in the preterm neonatal lamb
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Expression of select immune genes (surfactant proteins A and D, sheep beta defensin 1, and toll-like receptor 4) by respiratory epithelia is developmentally regulated in the preterm neonatal lamb

机译:在早产新生羔羊中,呼吸道上皮细胞表达的某些免疫基因(表面活性蛋白A和D,绵羊β防御素1和toll样受体4)的表达受到发育调控。

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摘要

Preterm infants experience enhanced susceptibility and severity to respiratory syncytial virus (RSV) infection. Terminal airway epithelium is an important site of RSV infection and the extent of local innate immune gene expression is poorly understood. In this study, expression of surfactant proteins A and D (SP-AD), sheep beta defensin I (SBD1), and toll-like receptor 4 (TLR4) mRNA were determined in whole lung homogenates from lambs. SP-AD and TLR4 mRNA expression increased (p < 0.05) from late gestation to term birth. In addition, gene expression of LCM-retrieved type 11 pneumocytes (CD208+), adjacent epithelium (CD208-) and bronchial epithelium demonstrated that bronchiole-alveolar junction epithelium (combined CD208+/-) had significant (p < 0.05) developmental increases in SP-AD, SBD1 and TLR4 mRNA, whereas CD208+ cells had statistically significant increases only with SP-A mRNA. Using immunofluorescence, SP-AD antigen distribution and intensity were also greater with developmental age. These studies show reduced SBD1, SP-AD, and TLR4 expression in the preterm lung and this may underlie enhanced RSV susceptibility. (c) 2006 Elsevier Ltd. All rights reserved.
机译:早产儿对呼吸道合胞病毒(RSV)感染的敏感性和严重性增强。气道末端上皮是RSV感染的重要部位,对局部先天免疫基因表达的程度了解甚少。在这项研究中,确定了羔羊全肺匀浆中表面活性剂蛋白A和D(SP-AD),绵羊β防御素I(SBD1)和toll样受体4(TLR4)mRNA的表达。从妊娠晚期到足月出生,SP-AD和TLR4 mRNA表达增加(p <0.05)。此外,LCM修复的11型肺炎细胞(CD208 +),邻近上皮细胞(CD208-)和支气管上皮细胞的基因表达表明,细支气管-肺泡连接上皮细胞(CD208 +/-合并)在SP-中具有显着(p <0.05)发育增加。 AD,SBD1和TLR4 mRNA,而CD208 +细胞仅SP-A mRNA具有统计学上的显着增加。使用免疫荧光,SP-AD抗原的分布和强度也随着年龄的增长而增加。这些研究表明早产肺中SBD1,SP-AD和TLR4的表达降低,这可能是RSV易感性增强的基础。 (c)2006 Elsevier Ltd.保留所有权利。

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