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. 1994 Apr;49(4):319–326. doi: 10.1136/thx.49.4.319

Collagen content of alveolar wall tissue in emphysematous and non-emphysematous lungs.

M R Lang 1, G W Fiaux 1, M Gillooly 1, J A Stewart 1, D J Hulmes 1, D Lamb 1
PMCID: PMC475363  PMID: 8202900

Abstract

BACKGROUND--Emphysema is currently defined as "a condition of the lung characterised by abnormal, permanent enlargement of the airspaces distal to the terminal bronchiole, accompanied by destruction of their walls, and without obvious fibrosis." The functional and morphological changes that occur in emphysema have largely been attributed to changes in alveolar elastin rather than in collagen. A study was performed to determine whether the amount of collagen in the alveolar wall changes with age in the lungs of non-smokers and of smokers with different types of macroscopically defined emphysema in relation to a microscopic measurement of lung structure. METHODS--Total alveolar wall collagen was measured (as hydroxyproline) in known volumes of distended lung tissue (by reverse phase high pressure liquid chromatography) in the lungs of non-smokers (n = 23) and in regions sampled away from emphysematous lesions in the lungs of 36 smokers (four with no emphysema, 13 with centriacinar emphysema (CAE), nine with panacinar emphysema (PAE), and 10 with a mixture (MIX) of both PAE and CAE). Mean lung airspace wall surface area per unit volume (AWUV) was calculated from at least six random blocks per lung and on histological sections immediately adjacent to those prepared for collagen measurement with a rapid scanning device (fast interval processor). RESULTS--In non-smokers there was no significant correlation between the amount of collagen in the alveolar wall tissue and either mean lung AWUV or increasing patient age when amounts of collagen were expressed either per unit volume of distended lung (40 mm3 sample) or per unit surface area of airspace wall tissue. Smokers without emphysema had similar amounts of collagen to non-smokers. Lungs with PAE and MIX, but not CAE alone, contained significantly more collagen than normal when expressed per unit volume of airspace wall tissue whereas all groups, including CAE, contained significantly raised amounts of collagen when expressed per unit surface area. CONCLUSIONS--There is no significant age related change in the collagen content of the lungs of non-smokers which suggests that, as AWUV is lost with age, the main collagenous framework is maintained. However, in smokers with emphysema there is a loss of airspace wall tissue in regions remote from the macroscopic lesions that is accompanied by a net increase in collagen mass. The greater accumulation of collagen in MIX lungs than in CAE lungs suggests a greater degree of structural damage, indicative of an alternative pathogenetic mechanism operating between the different types of emphysema. Our results suggest an active alveolar wall fibrosis in emphysema as a consequence of cigarette smoking. It is suggested that the definition of emphysema may require further revision to include such change.

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Selected References

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  1. Cardoso W. V., Sekhon H. S., Hyde D. M., Thurlbeck W. M. Collagen and elastin in human pulmonary emphysema. Am Rev Respir Dis. 1993 Apr;147(4):975–981. doi: 10.1164/ajrccm/147.4.975. [DOI] [PubMed] [Google Scholar]
  2. Chrzanowski P., Keller S., Cerreta J., Mandl I., Turino G. M. Elastin content of normal and emphysematous lung parenchyma. Am J Med. 1980 Sep;69(3):351–359. doi: 10.1016/0002-9343(80)90004-2. [DOI] [PubMed] [Google Scholar]
  3. Fitzpatrick M. Studies of human pulmonary connective tissue. III. Chemical changes in structural proteins with emphysema. Am Rev Respir Dis. 1967 Aug;96(2):254–265. doi: 10.1164/arrd.1967.96.2.254. [DOI] [PubMed] [Google Scholar]
  4. Gadek J. E., Fells G. A., Zimmerman R. L., Rennard S. I., Crystal R. G. Antielastases of the human alveolar structures. Implications for the protease-antiprotease theory of emphysema. J Clin Invest. 1981 Oct;68(4):889–898. doi: 10.1172/JCI110344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Gillooly M., Lamb D. Airspace size in lungs of lifelong non-smokers: effect of age and sex. Thorax. 1993 Jan;48(1):39–43. doi: 10.1136/thx.48.1.39. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Gillooly M., Lamb D., Farrow A. S. New automated technique for assessing emphysema on histological sections. J Clin Pathol. 1991 Dec;44(12):1007–1011. doi: 10.1136/jcp.44.12.1007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Janoff A. Elastases and emphysema. Current assessment of the protease-antiprotease hypothesis. Am Rev Respir Dis. 1985 Aug;132(2):417–433. doi: 10.1164/arrd.1985.132.2.417. [DOI] [PubMed] [Google Scholar]
  8. Kirk J. M., Da Costa P. E., Turner-Warwick M., Littleton R. J., Laurent G. J. Biochemical evidence for an increased and progressive deposition of collagen in lungs of patients with pulmonary fibrosis. Clin Sci (Lond) 1986 Jan;70(1):39–45. doi: 10.1042/cs0700039. [DOI] [PubMed] [Google Scholar]
  9. Lang M. R., Fiaux G. W., Hulmes D. J., Lamb D., Miller A. Quantitative studies of human lung airspace wall in relation to collagen and elastin content. Matrix. 1993 Nov;13(6):471–480. doi: 10.1016/s0934-8832(11)80113-7. [DOI] [PubMed] [Google Scholar]
  10. Laurent G. J. Lung collagen: more than scaffolding. Thorax. 1986 Jun;41(6):418–428. doi: 10.1136/thx.41.6.418. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Laurent G. J., McAnulty R. J., Corrin B., Cockerill P. Biochemical and histological changes in pulmonary fibrosis induced in rabbits with intratracheal bleomycin. Eur J Clin Invest. 1981 Dec;11(6):441–448. doi: 10.1111/j.1365-2362.1981.tb02011.x. [DOI] [PubMed] [Google Scholar]
  12. MEAD J. Mechanical properties of lungs. Physiol Rev. 1961 Apr;41:281–330. doi: 10.1152/physrev.1961.41.2.281. [DOI] [PubMed] [Google Scholar]
  13. PIERCE J. A., HOCOTT J. B., EBERT R. V. The collagen and elastin content of the lung in emphysema. Ann Intern Med. 1961 Aug;55:210–222. doi: 10.7326/0003-4819-55-2-210. [DOI] [PubMed] [Google Scholar]
  14. Rosenquist T. H. Organization of collagen in the human pulmonary alveolar wall. Anat Rec. 1981 Aug;200(4):447–459. doi: 10.1002/ar.1092000408. [DOI] [PubMed] [Google Scholar]
  15. Seyer J. M., Hutcheson E. T., Kang A. H. Collagen polymorphism in idiopathic chronic pulmonary fibrosis. J Clin Invest. 1976 Jun;57(6):1498–1507. doi: 10.1172/JCI108420. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Snider G. L., Karlinsky J. B. Relation between the elastic behavior and the connective tissues of the lungs. Pathobiol Annu. 1977;7:115–142. [PubMed] [Google Scholar]
  17. Stockley R. A. alpha-1-Antitrypsin and the pathogenesis of emphysema. Lung. 1987;165(2):61–77. doi: 10.1007/BF02714424. [DOI] [PubMed] [Google Scholar]
  18. Teerlink T., Tavenier P., Netelenbos J. C. Selective determination of hydroxyproline in urine by high-performance liquid chromatography using precolumn derivatization. Clin Chim Acta. 1989 Aug 31;183(3):309–315. doi: 10.1016/0009-8981(89)90365-3. [DOI] [PubMed] [Google Scholar]
  19. The definition of emphysema. Report of a National Heart, Lung, and Blood Institute, Division of Lung Diseases workshop. Am Rev Respir Dis. 1985 Jul;132(1):182–185. doi: 10.1164/arrd.1985.132.1.182. [DOI] [PubMed] [Google Scholar]

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