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PMID: 10201943 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Induction and regulation of macrophage metalloelastase by hyaluronan fragments in mouse macrophages.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 162 ·No. 7 ·1999-04-01 ·Pages 4171-6

Horton MR, Shapiro S, Bao C, Lowenstein CJ, Noble PW

Abstract

Although the metalloproteinase murine metalloelastase (MME) has been implicated in lung disorders such as emphysema and pulmonary fibrosis, the mechanisms regulating MME expression are unclear. Low m.w. fragments of the extracellular matrix component hyaluronan (HA) that accumulate at sites of lung inflammation are capable of inducing inflammatory gene expression in macrophages (Mphi). The purpose of this study was to examine the effect of HA fragments on the expression of MME in alveolar Mphi. The mouse alveolar Mphi cell line MH-S was stimulated with HA fragments over time, total RNA was isolated, and Northern blot analysis was performed. HA fragments induced MME mRNA in a time-dependent fashion, with maximal levels at 6 h. HA fragments also induced MME protein expression as well as enzyme activity. The induction of MME gene expression was specific for low m.w. HA fragments and dependent upon new protein synthesis; it occurred at the level of gene transcription. We also examined the effect of HA fragments on MME expression in inflammatory alveolar Mphi from bleomycin-injured rat lungs. Although normal rat alveolar Mphi did not express MME mRNA in response to HA fragments, alveolar Mphi from the bleomycin-treated rats responded to HA fragment stimulation by increasing MME mRNA levels. Furthermore, baseline and HA fragment-induced MME gene expression in alveolar Mphi from bleomycin-treated rats was inhibited by IFN-gamma. These data suggest that HA fragments may be an important mechanism for the expression of MME by Mphi in inflammatory lung disorders.

MeSH Terms
Animals Bleomycin/pharmacology Cell Line Disease Models, Animal Dose-Response Relationship, Immunologic Enzyme Activation/drug effects,immunology Enzyme Induction/drug effects,immunology Female Humans Hyaluronic Acid/pharmacology Macrophages, Alveolar/drug effects,enzymology Male Matrix Metalloproteinase 12 Metalloendopeptidases/biosynthesis,genetics,metabolism Mice Mice, Inbred C3H Molecular Weight Protein Biosynthesis RNA, Messenger/biosynthesis Rats Rats, Sprague-Dawley
Chemicals
RNA, Messenger Bleomycin Hyaluronic Acid Metalloendopeptidases MMP12 protein, human Matrix Metalloproteinase 12
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Horton M R
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Shapiro S
Bao C
Lowenstein C J
Noble P W
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1999-04-01
Pages
4171-6
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NHLBI NIH HHS · 5F32HL09614-02 · United States
NHLBI NIH HHS · K11HL02880 · United States
NHLBI NIH HHS · R01HL60539 · United States
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