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PMID: 2679263 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Macrophage-derived growth factors in wound healing: regulation of growth factor production by the oxygen microenvironment.

The American review of respiratory disease ·Vol. 140 ·No. 4 ·1989-10-00 ·Pages 1108-11

Knighton DR, Fiegel VD

Abstract

There is a large amount of current research investigating the pathophysiologic aspects of pulmonary hypertension. Results of this research indicate the potential role of the macrophage as one possible mediator of pulmonary hypertension. The macrophage has been shown to produce numerous soluble mediators, including various growth factors, some of which may be involved in the cellular proliferation of the arterial wall. Most of the knowledge regarding oxygen microenvironments, macrophages, and growth factor production comes from research on the healing wound. A considerable amount of what has been learned about the role of the macrophage in cutaneous wound healing may have direct applicability to macrophage function in acute lung injury and repair, and pulmonary hypertension. Macrophages play a pivotal role in cutaneous wound repair. They participate in immunologic and nonspecific host defense responses and produce numerous growth factors that regulate mesenchymal cell proliferation, migration, and synthesis of extracellular matrix proteins. These same responses are probably at work during the progression of pulmonary hypertension.

MeSH Terms
Growth Substances/biosynthesis,physiology Humans Macrophages/physiology Oxygen/pharmacology Oxygen Consumption Wound Healing
Chemicals
Growth Substances Oxygen
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Knighton D R
Department of Surgery, University of Minnesota, Minneapolis 55455.
Fiegel V D
Article Info
Journal
The American review of respiratory disease
Abbr.
Am Rev Respir Dis
ISSN
0003-0805
Published
1989-10-00
Pages
1108-11
Language
English
Region
United States
NLM ID
0370523
Subset
IM
Grants
NIGMS NIH HHS · GM-35442-02 · United States
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