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PMID: 9302297 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Requirement for macrophage elastase for cigarette smoke-induced emphysema in mice.

Science (New York, N.Y.) ·Vol. 277 ·No. 5334 ·1997-09-26 ·Pages 2002-4

Hautamaki RD, Kobayashi DK, Senior RM, Shapiro SD

Abstract

To determine which proteinases are responsible for the lung destruction characteristic of pulmonary emphysema, macrophage elastase-deficient (MME-/-) mice were subjected to cigarette smoke. In contrast to wild-type mice, MME-/- mice did not have increased numbers of macrophages in their lungs and did not develop emphysema in response to long-term exposure to cigarette smoke. Smoke-exposed MME-/- mice that received monthly intratracheal instillations of monocyte chemoattractant protein-1 showed accumulation of alveolar macrophages but did not develop air space enlargement. Thus, macrophage elastase is probably sufficient for the development of emphysema that results from chronic inhalation of cigarette smoke.

MeSH Terms
Animals Cell Count Chemokine CCL2/pharmacology Gene Targeting Lung/pathology Macrophages, Alveolar/enzymology,physiology Matrix Metalloproteinase 12 Metalloendopeptidases/genetics,metabolism Mice Mice, Inbred C57BL Mice, Inbred Strains Neutrophils Plants, Toxic Pulmonary Alveoli/pathology Pulmonary Emphysema/enzymology,etiology,pathology Smoke/adverse effects Smoking/adverse effects Tobacco
Chemicals
Chemokine CCL2 Smoke Metalloendopeptidases Matrix Metalloproteinase 12
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hautamaki R D
Department of Internal Medicine, Washington University School of Medicine at Barnes-Jewish Hospital, St. Louis, MO 63110, USA.
Kobayashi D K
Senior R M
Shapiro S D
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1997-09-26
Pages
2002-4
Language
English
Region
United States
NLM ID
0404511
Subset
IM
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