Dik Willem A, van Kaam Anton H L C, Dekker Tamara, Naber Brigitta A E, Janssen Daphne J, Kroon A A, Zimmermann Luc J I, Versnel Marjan A, Lutter René
Department of Immunology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Biol Neonate. 2006;89(1):6-14. doi: 10.1159/000088193. Epub 2005 Sep 8.
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).
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.
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.
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.
基质金属蛋白酶(MMPs)在气道损伤和重塑中起重要作用。我们探讨了这样一个假设,即出生后早期(2 - 4天),呼吸窘迫综合征(RDS)病情好转的婴儿与发生早产儿慢性肺病(CLD)的婴儿之间,肺MMP水平会有所不同。
纳入32例诊断为RDS的早产儿(胎龄≤30周)。其中13例婴儿的RDS病情好转,19例发展为CLD。通过酶谱分析和光密度测定法分析出生后第2、4、7和10天收集的支气管肺泡灌洗(BAL)液中的MMP - 2和MMP - 9。对BAL细胞和肺组织进行免疫化学分析,以确定RDS和CLD中MMP - 9的细胞来源。
与CLD患者(MMP - 9 = 5.4任意单位(AU))相比,RDS病情好转患者的BAL液中MMP - 9水平在第2天显著升高(MMP - 9中位数 = 42.0 AU)。与CLD(MMP - 9 = 25.4 AU;NGAL = 2.0 AU)相比,RDS病情好转患者的BAL液中MMP - 9和中性粒细胞脂质运载蛋白相关MMP - 9(NGAL)在第4天显著更高(MMP - 9 = 65.8 AU;NGAL = 16.1 AU),CLD患者的MMP - 9和NGAL水平在第7天和第10天随后升高。RDS和CLD之间未检测到MMP - 2水平的差异。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。
我们的研究结果表明,RDS病情好转和CLD发生过程中,早期BAL液中MMP - 9水平存在差异,这可能与对初始损伤做出早期充分反应的能力有关。