Early increased levels of matrix metalloproteinase-9 in neonates recovering from respiratory distress syndrome.

Biology of the neonate Pub Date : 2006-01-01 Epub Date: 2005-09-08 DOI:10.1159/000088193
Willem A Dik, Anton H L C van Kaam, Tamara Dekker, Brigitta A E Naber, Daphne J Janssen, A A Kroon, Luc J I Zimmermann, Marjan A Versnel, René Lutter
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引用次数: 35

Abstract

Aim: Matrix metalloproteinases (MMPs) play an eminent role in airway injury and remodelling. We explored the hypothesis that pulmonary MMP levels would differ early after birth (2-4 days) between infants with resolving respiratory distress syndrome (RDS) and infants developing chronic lung disease of prematurity (CLD).

Methods: Thirty-two prematurely born infants (gestational age < or =30 weeks) diagnosed with RDS were included. In 13 infants RDS resolved while 19 developed CLD. MMP-2 and MMP-9 in bronchoalveolar lavage (BAL) fluids collected on postnatal days 2, 4, 7 and 10 were analyzed by zymography and densitometry. Immunochemistry was performed on BAL cells and lung tissue to identify cellular sources of MMP-9 in RDS and CLD.

Results: Median MMP-9 levels increased significantly on day 2 in BAL fluid from patients with resolving RDS (median values MMP-9 = 42.0 arbitrary units (AU)) compared to CLD patients (MMP-9 = 5.4 AU). MMP-9 and neutrophil lipocalin-associated MMP-9 (NGAL) were significantly higher on day 4 in BAL fluid from resolving RDS (MMP-9 = 65.8 AU; NGAL = 16.1 AU) compared to CLD (MMP-9 = 25.4 AU; NGAL = 2.0 AU), Levels of MMP-9 and NGAL increased subsequently on days 7 and 10 in CLD. No differences in MMP-2 levels were detected between RDS and CLD. Neutrophils, macrophages and alveolar type-II epithelial cells were identified as potential sources of MMP-9.

Conclusion: Our findings indicate differences in early MMP-9 BAL fluid levels between resolving RDS and developing CLD, which may relate to the ability to raise an early and adequate response to the initial injury.

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呼吸窘迫综合征恢复期新生儿基质金属蛋白酶-9水平早期升高
目的:基质金属蛋白酶(MMPs)在气道损伤和气道重构中起重要作用。我们探讨了呼吸窘迫综合征(RDS)患儿和慢性早产儿肺病(CLD)患儿在出生后(2-4天)早期肺部MMP水平的差异。方法:入选32例胎龄<或=30周的早产RDS患儿。13例患儿RDS消退,19例患儿CLD。对出生后第2、4、7和10天收集的支气管肺泡灌洗液中的MMP-2和MMP-9进行酶谱分析和密度测定。采用免疫化学方法对BAL细胞和肺组织进行检测,以确定RDS和CLD中MMP-9的细胞来源。结果:与CLD患者(MMP-9 = 5.4 AU)相比,缓解RDS患者BAL液中的中位MMP-9水平在第2天显著升高(中位值MMP-9 = 42.0任意单位(AU))。MMP-9和中性粒细胞脂钙素相关的MMP-9 (NGAL)在第4天在解决RDS的BAL液中显著升高(MMP-9 = 65.8 AU;NGAL = 16.1 AU),而CLD (MMP-9 = 25.4 AU;NGAL = 2.0 AU), MMP-9和NGAL水平随后在CLD的第7天和第10天升高。在RDS和CLD之间检测到MMP-2水平无差异。中性粒细胞、巨噬细胞和肺泡ii型上皮细胞被确定为MMP-9的潜在来源。结论:我们的研究结果表明,缓解RDS和发展CLD的早期MMP-9 BAL液水平存在差异,这可能与早期对初始损伤做出充分反应的能力有关。
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