Skip to main content
Environmental Health Perspectives logoLink to Environmental Health Perspectives
. 2000 Nov;108(11):1063–1069. doi: 10.1289/ehp.001081063

Distribution of particulate matter and tissue remodeling in the human lung.

K E Pinkerton 1, F H Green 1, C Saiki 1, V Vallyathan 1, C G Plopper 1, V Gopal 1, D Hung 1, E B Bahne 1, S S Lin 1, M G Ménache 1, M B Schenker 1
PMCID: PMC1240164  PMID: 11102298

Abstract

We examined the relationship between intrapulmonary particle distribution of carbonaceous and mineral dusts and remodeling of the airways along anatomically distinct airway paths in the lungs of Hispanic males from the central valley of California. Lung autopsy specimens from the Fresno County Coroner's Office were prepared by intratracheal instillation of 2% glutaraldehyde at 30 cm H(2)O pressure. Two distinct airway paths into the apico-posterior and apico-anterior portions of the left upper lung lobe were followed. Tissue samples for histologic analysis were generally taken from the intrapulmonary second, fourth, sixth, and ninth airway generations. Parenchymal tissues beyond the 12th airway generation of each airway path were also analyzed. There was little evidence of visible particle accumulation in the larger conducting airways (generations 2-6), except in bronchial-associated lymphoid tissues and within peribronchial connective tissue. In contrast, terminal and respiratory bronchioles arising from each pathway revealed varying degrees of wall thickening and remodeling. Walls with marked thickening contained moderate to heavy amounts of carbonaceous and mineral dusts. Wall thickening was associated with increases in collagen and interstitial inflammatory cells, including dust-laden macrophages. These changes were significantly greater in first-generation respiratory bronchioles compared to second- and third-generation respiratory bronchioles. These findings suggest that accumulation of carbonaceous and mineral dust in the lungs is significantly affected by lung anatomy with the greatest retention in centers of lung acini. Furthermore, there is significant remodeling of this transitional zone in humans exposed to ambient particulate matter.

Full Text

The Full Text of this article is available as a PDF (653.8 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Adesina A. M., Vallyathan V., McQuillen E. N., Weaver S. O., Craighead J. E. Bronchiolar inflammation and fibrosis associated with smoking. A morphologic cross-sectional population analysis. Am Rev Respir Dis. 1991 Jan;143(1):144–149. doi: 10.1164/ajrccm/143.1.144. [DOI] [PubMed] [Google Scholar]
  2. Churg A., Brauer M. Human lung parenchyma retains PM2.5. Am J Respir Crit Care Med. 1997 Jun;155(6):2109–2111. doi: 10.1164/ajrccm.155.6.9196123. [DOI] [PubMed] [Google Scholar]
  3. Churg A., Wright J. L., Stevens B. Exogenous mineral particles in the human bronchial mucosa and lung parenchyma. I. Nonsmokers in the general population. Exp Lung Res. 1990 May-Jun;16(3):159–175. doi: 10.3109/01902149009108838. [DOI] [PubMed] [Google Scholar]
  4. Cosio M. G., Hale K. A., Niewoehner D. E. Morphologic and morphometric effects of prolonged cigarette smoking on the small airways. Am Rev Respir Dis. 1980 Aug;122(2):265–221. doi: 10.1164/arrd.1980.122.2.265. [DOI] [PubMed] [Google Scholar]
  5. Craighead J. E., Abraham J. L., Churg A., Green F. H., Kleinerman J., Pratt P. C., Seemayer T. A., Vallyathan V., Weill H. The pathology of asbestos-associated diseases of the lungs and pleural cavities: diagnostic criteria and proposed grading schema. Report of the Pneumoconiosis Committee of the College of American Pathologists and the National Institute for Occupational Safety and Health. Arch Pathol Lab Med. 1982 Oct 8;106(11):544–596. [PubMed] [Google Scholar]
  6. Darquenne C., Paiva M. Two- and three-dimensional simulations of aerosol transport and deposition in alveolar zone of human lung. J Appl Physiol (1985) 1996 Apr;80(4):1401–1414. doi: 10.1152/jappl.1996.80.4.1401. [DOI] [PubMed] [Google Scholar]
  7. Diseases associated with exposure to silica and nonfibrous silicate minerals. Silicosis and Silicate Disease Committee. Arch Pathol Lab Med. 1988 Jul;112(7):673–720. [PubMed] [Google Scholar]
  8. Federspiel W. J., Fredberg J. J. Axial dispersion in respiratory bronchioles and alveolar ducts. J Appl Physiol (1985) 1988 Jun;64(6):2614–2621. doi: 10.1152/jappl.1988.64.6.2614. [DOI] [PubMed] [Google Scholar]
  9. Harkema J. R., Plopper C. G., Hyde D. M., St George J. A., Wilson D. W., Dungworth D. L. Response of macaque bronchiolar epithelium to ambient concentrations of ozone. Am J Pathol. 1993 Sep;143(3):857–866. [PMC free article] [PubMed] [Google Scholar]
  10. Lippmann M., Yeates D. B., Albert R. E. Deposition, retention, and clearance of inhaled particles. Br J Ind Med. 1980 Nov;37(4):337–362. doi: 10.1136/oem.37.4.337. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Nieuwenhuijsen M. J., Kruize H., Schenker M. B. Exposure to dust and its particle size distribution in California agriculture. Am Ind Hyg Assoc J. 1998 Jan;59(1):34–38. doi: 10.1080/15428119891010316. [DOI] [PubMed] [Google Scholar]
  12. Niewoehner D. E., Kleinerman J., Rice D. B. Pathologic changes in the peripheral airways of young cigarette smokers. N Engl J Med. 1974 Oct 10;291(15):755–758. doi: 10.1056/NEJM197410102911503. [DOI] [PubMed] [Google Scholar]
  13. Sherwin R. P., Barman M. L., Abraham J. L. Silicate pneumoconiosis of farm workers. Lab Invest. 1979 May;40(5):576–582. [PubMed] [Google Scholar]
  14. Thun M. J., Lally C. A., Flannery J. T., Calle E. E., Flanders W. D., Heath C. W., Jr Cigarette smoking and changes in the histopathology of lung cancer. J Natl Cancer Inst. 1997 Nov 5;89(21):1580–1586. doi: 10.1093/jnci/89.21.1580. [DOI] [PubMed] [Google Scholar]
  15. Thurlbeck W. M., Ryder R. C., Sternby N. A comparative study of the severity of emphysema in necropsy populations in three different countries. Am Rev Respir Dis. 1974 Feb;109(2):239–248. doi: 10.1164/arrd.1974.109.2.239. [DOI] [PubMed] [Google Scholar]
  16. Tsuda A., Henry F. S., Butler J. P. Chaotic mixing of alveolated duct flow in rhythmically expanding pulmonary acinus. J Appl Physiol (1985) 1995 Sep;79(3):1055–1063. doi: 10.1152/jappl.1995.79.3.1055. [DOI] [PubMed] [Google Scholar]
  17. Tsuda S., Iwasaki M., Yoshida M., Shirasu Y. Inhalation chamber with size discriminator for liquid aerosols. Fundam Appl Toxicol. 1984 Jun;4(3 Pt 1):378–387. doi: 10.1016/0272-0590(84)90195-7. [DOI] [PubMed] [Google Scholar]
  18. Wright J. L., Cagle P., Churg A., Colby T. V., Myers J. Diseases of the small airways. Am Rev Respir Dis. 1992 Jul;146(1):240–262. doi: 10.1164/ajrccm/146.1.240. [DOI] [PubMed] [Google Scholar]

Articles from Environmental Health Perspectives are provided here courtesy of National Institute of Environmental Health Sciences

RESOURCES