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Type I collagenases in bronchoalveolar lavage fluid from preterm babies at risk of developing chronic lung disease
  1. D G Sweeta,
  2. K J McMahonb,
  3. A E Curleya,
  4. C M O'Connorb,
  5. H L Hallidaya
  1. aDepartment of Child Health, The Queen's University of Belfast and Regional Neonatal Unit, Royal Maternity Hospital, Belfast, Northern Ireland, bDepartment of Medicine and Therapeutics, University College Dublin, Republic of Ireland
  1. Dr Sweet, Perinatal Room, Royal Maternity Hospital, Grosvenor Road, Belfast BT12 6BB, Northern Irelanddsweet{at}dnet.co.uk

Abstract

OBJECTIVE To assess whether increased collagenolysis precedes severe chronic lung disease (CLD).

METHODS Matrix metalloproteinase-1 (MMP-1) and MMP-8 (enzymes that degrade type I collagen, the main structural protein of lung extracellular matrix) were measured by enzyme linked immunosorbent assay in 100 bronchoalveolar lavage samples taken during the first 6 postnatal days from 45 ventilated preterm babies < 33 weeks gestation. The median value for each baby was calculated. CLD was defined as an oxygen requirement after the 36th week after conception.

RESULTS MMP-8 levels in bronchoalveolar lavage fluid were higher (median 13 ng/ml) in 20 babies who developed CLD than in 25 without CLD (median 2 ng/ml). No MMP-1 was detected in any sample.

CONCLUSIONS MMP-8 can be detected in bronchoalveolar lavage fluid from preterm babies, and higher levels are found in those who later develop CLD. MMP-8 may contribute to lung injury that occurs as a prelude to CLD.

  • chronic lung disease
  • lungs
  • collagen
  • extracellular matrix
  • matrix metalloproteinase
  • preterm

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Improved antenatal care, along with advances in neonatal intensive care, have resulted in greater numbers of very preterm babies surviving who are at risk of developing chronic lung disease (CLD).1 The exact mechanisms underlying the lung injury and airways remodelling in CLD are not clear, but mechanical ventilation, oxygen toxicity, and inflammation all play a role.2-6 It is hypothesised that inflammation may directly damage the lung by increasing the release of proteolytic enzymes that degrade components of the lung interstitium. Both elastase7 and matrix metalloproteinase (MMP)-9, which is a type IV collagenase, are increased in the lungs of babies who later develop CLD.8

Lung biomechanical properties are largely dependent on the correct distribution and abundance of the extracellular matrix which is also crucial in maintaining the alignment and differentiated state of the various epithelial cell layers lining the airways.9Preterm babies born before 28 weeks gestation are just starting to develop a pulmonary capillary bed and are beginning the process of alveolarisation of the distal saccules. Lung injury during this crucial period of remodelling may result in arrest of lung development.10

MMPs are enzymes required to support and maintain the extracellular matrix.11 12 Type I collagen is the major structural protein of the extracellular matrix, and MMP-1 and MMP-8 are the only proteinases that degrade type I collagen.13 Excess MMP-8 activity has been implicated in adult lung diseases such as emphysema14 15 and bronchiectasis.16 In this study, we measured MMP-1 and MMP-8 levels in bronchoalveolar lavage (BAL) fluid from preterm babies within the first week of life to determine if excessive type I collagenolysis is implicated in the development of severe CLD.

Patients and methods

This was a prospective study of babies born in the Royal Maternity Hospital in Belfast. The research ethics committee of The Queen's University of Belfast gave approval for the study, and parental consent was obtained before babies were enrolled.

Forty five babies of less than 33 weeks gestation were recruited when they required intubation and mechanical ventilation in the first 6 days of life. Gestation was estimated by duration of amenorrhoea combined with early ultrasound measurement. Serial BAL was performed daily whenever possible from the time of intubation until extubation or the 6th day of life, whichever was soonest. Babies were only studied when clinically stable and not during the 12 hours after a dose of surfactant. After extubation, the babies' progress was monitored until discharge or the 36th week after conception. For the purposes of this study, severe CLD was defined as a requirement for supplemental oxygen to maintain oxygen saturation measured by pulse oximetry above 92% when at rest after the 36th week after conception. The severity of the initial respiratory disease was compared using the median arterial-alveolar oxygen tension ratio (a/A ratio) in the first 24 hours of life. This was calculated from arterial blood gases using the equation: a/A ratio = Pao 2/((96 × Fio 2) − Paco 2)

where Pao 2 and Paco 2 are expressed in kPa and Fio 2 as a fraction of 1.

METHOD FOR BAL

BAL was performed in a standardised way using a well established technique,5 although unlike the study by Kotechaet al no marker of dilution was used. This is in accordance with the most recent European Respiratory Society guidelines on BAL.17 In summary, 1 ml/kg sterile 0.9% saline was instilled using a 2 ml syringe through a 5F gauge feeding catheter which had been placed via the endotracheal tube into the distal right main bronchus. The saline was instilled and immediately aspirated back into the syringe. The median volume of saline returned was 0.7 ml (interquartile range (IQR) 0.5–1.2 ml). The sample was clarified by centrifugation at 1500 g for five minutes at room temperature, and the supernatant immediately frozen at −70°C and kept for subsequent analysis.

LABORATORY METHODS

Samples were assayed for MMP-1 and MMP-8 by commercial enzyme linked immunosorbent assay (ELISA) in accordance with the manufacturer's instructions (Amersham International, Amersham, Bucks, UK). The ELISA systems measure total levels of their respective antigens, including latent and active forms of the MMPs and MMP/tissue inhibitor of metalloproteinase (TIMP) complexes. The sensitivity of the MMP-8 assay was 0.032 ng/ml (range 0.032–4 ng/ml), and that of the MMP-1 assay was 1.7 ng/ml (range 1.7–100 ng/ml). The ability of the MMP-1 assay to detect this enzyme in dilute biological fluids was confirmed by analysis of supernatants from phorbol myristrate acetate stimulated alveolar macrophages. All samples were assayed in duplicate.

STATISTICAL ANALYSIS

To simplify statistical analysis of changes over time, postnatal age was divided into 48 hour time periods. If more than one sample from an individual baby was taken within a time period, the median result was used. Median MMP levels were calculated for each baby and used as the summary statistic. MMP-8 levels were not normally distributed, so non-parametric statistical tests were used. The logarithm of MMP-8 concentration was normally distributed and used in the logistic regression analyses. Spearman correlations, Mann-Whitney U tests, Wilcoxon signed rank test, χ2 and regression analysis were all calculated using STATVIEW for Windows version 4.57 1996 (Abacus Concepts Inc, Berkeley, California, USA).

Results

A total of 100 BAL samples were collected for analysis. Twenty of the 45 babies studied developed severe CLD. They were less mature and lighter at birth than those who did not, but there was no significant difference in initial severity of respiratory distress, as assessed by the a/A Po 2 ratio during the first 24 hours (table 1). There was a preponderance of boys in both groups.

Table 1

Clinical characteristics of babies studied

MMP-1 was not detected in any BAL samples. MMP-8 was detected in 68 of the 100 BAL samples. For all 100 BAL samples, MMP-8 levels did not change significantly with increasing postnatal age (r = 0.17; p = 0.1). Analysis of MMP-8 levels was also carried out on infants who had samples taken during both the 0–48 and 49–96 hour periods. MMP-8 levels did not vary significantly with postnatal age in this group (median (IQR) at 0–48 hours, 2.5 (0.03–17.2) ng/ml; at 49–96 hours, 8.1 (4.5–31.9) ng/ml). Each baby had on average two BAL samples taken (range 1–5). Babies who subsequently developed CLD tended to have more samples taken over the six day period. MMP-8 levels were higher throughout the first six days in babies who developed CLD, but because of the small number of samples, this result was only statistically significant between 49 and 96 hours of age (fig 1).

Figure 1

Postnatal changes in matrix metalloproteinase-8 (MMP-8) concentrations in bronchoalveolar lavage (BAL) fluid from babies who later developed chronic lung disease (CLD) and those who did not. Data depicting medians and 75th percentiles are presented on a log scale. MMP-8 levels were higher in babies who later developed CLD. No CLD v CLD: at 0–48 hours, median 0.25 v 5 ng/ml (p = 0.16); at 49–96 hours, median 3 v 9 ng/ml (p = 0.006); at 97–144 hours, median 7 v 14 ng/ml (p = 0.51).

The use of median MMP-8 levels as the summary statistic for each baby showed that MMP-8 levels were negatively correlated with gestational age (r = −0.35; p = 0.01) and birth weight (r = −0.32; p = 0.02). Median MMP-8 levels were about 10-fold higher in babies who subsequently developed CLD (fig 2).

Figure 2

By using all the bronchoalveolar lavage samples, median matrix metalloproteinase-8 (MMP-8) concentration was calculated for each baby. The distribution of these medians is indicated using box and whisker plots that show medians, 25th and 75th percentiles, and the full range. Median MMP-8 levels were significantly higher in babies who subsequently developed severe chronic lung disease (CLD) than in those who did not (13 v 2 ng/ml; p = 0.001).

To avoid the bias of more samples being taken from babies who developed CLD, the 74 samples taken within the first four postnatal days were also analysed in isolation. Forty two babies were available for study, of whom 17 developed CLD. The proportion of babies in whom MMP-8 was detected was significantly higher in the CLD group than in the no CLD group (15/17 (88%) v 14/25 (56%); p = 0.026) and the difference in MMP-8 levels remained significantly higher (median (IQR) 9 (5–32) v 2 (0–6) ng/ml; p = 0.0039).

All 45 babies were used in a multiple logistic regression model to assess factors that could influence the likelihood of developing CLD. Gestation, birth weight, median a/A ratio on day 1, sex, and log MMP-8 were tested, and of these only gestation (p < 0.0001), birth weight (p < 0.0001), and log MMP-8 (p = 0.0012) were individually predictive of CLD.

Discussion

Inflammation and neutrophil chemotaxis are essential prerequisites for the development of CLD. Neutrophil counts in tracheal aspirate are 20-fold higher on the third day of life in babies who later develop CLD than in those who do not.18 Neutrophil influx into the lungs probably contributes to tissue degradation by release of proteinases. We have previously shown that type IV collagenase (MMP-9) levels are increased in BAL fluid from babies who subsequently develop CLD and that there is an imbalance between MMP-9 and one of its major inhibitors, TIMP-1.8 Type IV collagen is the major constituent of basement membranes. Disruption of the basement membranes may explain the increased lung permeability observed in babies who develop CLD,4 but cannot explain all of the gross structural changes found in the lungs of babies with established CLD. We hypothesised that early destruction of the interstitial collagens in neonatal respiratory distress syndrome and matrix destruction may also be an important precursor to the development of structural remodelling of the airways.19

MMP-1 is a 55 kDa enzyme also known as interstitial collagenase or fibroblast type collagenase. It is released by a wide variety of stromal cells including fibroblasts, endothelial cells, osteoblasts, and chondroblasts. It will digest all major components of the extracellular matrix but it will preferentially degrade type III collagen. Its main function is during tissue homoeostasis and wound repair. MMP-8, or neutrophil collagenase, is a 75 kDa enzyme which is predominantly expressed by neutrophils, although some studies suggest that it can be expressed by other cells.20 21 MMP-8 also digests all major components of the extracellular matrix, but will preferentially degrade type I collagen.22 These two collagenases have a unique ability to cleave the native helix of fibrillar collagen by hydrolysing a single bond located one quarter length from the collagen C terminus.23 This process yields one quarter and three quarter fragments that at body temperature will spontaneously denature into randomly coiled gelatin peptides. Other members of the MMP family will then further degrade these into hydroxyproline. We have shown a 10-fold increase in median MMP-8 concentrations in BAL fluid from babies who subsequently develop severe CLD, suggesting that this enzyme may contribute to the early tissue destruction. Dissolution of the main structural framework of the lung matrix is likely to result in disorganisation of the lung architecture during healing. This may explain why lungs of babies with CLD have fewer than normal larger alveoli.24 We did not detect MMP-1 in any of the neonatal samples. This may reflect the less sensitive nature of the assay system (1.7 ng/ml for MMP-1v 0.032 ng/ml for MMP-8). Although MMP-1 levels within the assay range were measurable in conditioned medium from phorbol myristrate acetate stimulated macrophages, even these were at the lower end of the assay standard curve (< 10 ng/ml). Given the dilution effect inherent in sampling airway fluids by BAL, it is likely that the failure to detect MMP-1 was a consequence of this dilution. Although sample availability constraints did not allow for assessment of lining fluid dilution, such measurements would not have assisted in addressing this issue.

As indicated above, the major source of MMP-8 is the inflammatory neutrophil. Neutrophil derived MMPs are stored within intracellular granules and are released during neutrophil activation along with other neutrophil products, including the reactive oxygen radicals of the oxidative burst.25 MMP activity may also be influenced by oxidative stress, which is believed to be important in the pathogenesis of CLD. In a rat model, hyperoxia has been shown to increase expression of mRNA for MMP-8, with associated increased collagenase activity.26 Oxygen free radicals can activate pro-MMP-3, a proteinase that in turn will activate the latent form of MMP-8 in the tissues.27 TIMP-1, a major inhibitor of MMP activity, can be inactivated by oxygen free radicals, which may further tip the balance in favour of matrix degradation.28

A predictive test for CLD would be useful for determining which babies may benefit from early interventions to limit inflammation. In this study, MMP-8 was detected in 88% of the babies who developed CLD compared with 56% of those who did not develop CLD, but it is clear that, although this difference is statistically significant, it is unlikely that this measure in isolation will prove to be a useful predictive test.

In summary, we detected MMP-8, but not MMP-1, in BAL fluid from preterm babies at risk of developing CLD. There was a greater likelihood of MMP-8 being present if the baby subsequently developed severe CLD, and median MMP-8 levels were about 10-fold higher in the babies who developed CLD. We speculate that MMP-8 activity in the preterm lung may contribute to the lung damage that occurs in the early stages of CLD.

Acknowledgments

This project was supported by a grant from the Northern Ireland Mother & Baby Appeal.

References

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