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PMID: 11641248 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Fibrocytes induce an angiogenic phenotype in cultured endothelial cells and promote angiogenesis in vivo.

Hartlapp I, Abe R, Saeed RW, Peng T, Voelter W, Bucala R, Metz CN

Abstract

Angiogenesis is an ordered process requiring the inter-play of numerous cellular and humoral factors. Studies over the past 20 years have identified several growth factors, cytokines, and enzymes that promote blood vessel formation. Most have revealed how individual factors promote an angiogenic phenotype in endothelial cells in vitro or contribute to blood vessel formation in vivo. However, the fundamental question that remains unanswered is how the cellular microenvironment contributes to angiogenesis. Fibrocytes are a recently characterized mesenchymal cell type isolated from peripheral blood that rapidly enter subcutaneously implanted wound chambers and sites of tissue injury. Here we describe the induction of an angiogenic phenotype in microvascular endothelial cells in vitro and promotion of angiogenesis in vivo by cultured fibrocytes. Fibrocytes constitutively secrete extracellular matrix-degrading enzymes, primarily matrix metalloproteinase 9, which promotes endothelial cell invasion. In addition, fibrocytes secrete several proangiogenic factors including VEGF, bFGF, IL-8, PDGF, and hematopoietic growth factors that promote endothelial cell migration, proliferation, and/or tube formation. By contrast, they do not produce representative antiangiogenic factors. Finally, both autologous fibrocytes and fibrocyte-conditioned media were found to induce blood vessel formation in vivo using the Matrigel angiogenesis model.

MeSH Terms
3T3 Cells Animals Biological Factors/pharmacology Cell Differentiation Cell Division Cell Movement Cells, Cultured Culture Media, Conditioned/pharmacology Endothelium, Vascular/anatomy & histology,cytology,physiology Fibroblasts/physiology Growth Substances/pharmacology Humans Matrix Metalloproteinase 9/biosynthesis,genetics Mesoderm/cytology Mice Neovascularization, Physiologic/drug effects Phenotype Wound Healing
Chemicals
Biological Factors Culture Media, Conditioned Growth Substances Matrix Metalloproteinase 9
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Hartlapp I
Laboratory of Vascular Biology, The Picower Institute for Medical Research, Manhasset, New York 11030, USA.
Abe R
Saeed R W
Peng T
Voelter W
Bucala R
Metz C N
Article Info
Journal
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Abbr.
FASEB J
ISSN
1530-6860
Published
2001-10-00
Pages
2215-24
Language
English
Region
United States
NLM ID
8804484
Subset
IM
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