PUBLICATION

Lipocalin-7 Is a Matricellular Regulator of Angiogenesis

Authors
Brown, L.J., Alawoki, M., Crawford, M.E., Reida, T., Sears, A., Torma, T., and Albig, A.R.
ID
ZDB-PUB-101122-24
Date
2010
Source
PLoS One   5(11): e13905 (Journal)
Registered Authors
Keywords
none
MeSH Terms
  • Sequence Homology, Amino Acid
  • Cell Line
  • Neoplasm Proteins/genetics
  • Neoplasm Proteins/metabolism
  • Neoplasm Proteins/pharmacology*
  • Transforming Growth Factor beta/pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Aorta/drug effects
  • Aorta/physiology
  • Mice, Inbred C57BL
  • Molecular Sequence Data
  • Amino Acid Sequence
  • Recombinant Proteins/metabolism
  • Recombinant Proteins/pharmacology
  • Cell Proliferation/drug effects
  • Mice
  • In Vitro Techniques
  • Neovascularization, Physiologic/drug effects*
  • Animals
  • Gene Knockdown Techniques
  • Zebrafish/embryology
  • Zebrafish/genetics
  • Cell Movement/drug effects*
  • Blotting, Western
  • Gene Expression
  • Lipocalins/genetics
  • Lipocalins/metabolism
  • Lipocalins/pharmacology*
  • Endothelial Cells/drug effects*
  • Endothelial Cells/metabolism
  • Endothelial Cells/physiology
  • Embryo, Nonmammalian/embryology
  • Embryo, Nonmammalian/metabolism
(all 33)
PubMed
21085487 Full text @ PLoS One
Abstract
BACKGROUND: Matricellular proteins are extracellular regulators of cellular adhesion, signaling and performing a variety of physiological behaviors such as proliferation, migration and differentiation. Within vascular microenvironments, matricellular proteins exert both positive and negative regulatory cues to vascular endothelium. The relative balance of these matricellular cues is believed to be critical for vascular homeostasis, angiogenesis activation or angiogenesis resolution. However, our knowledge of matricellular proteins within vascular microenvironments and the mechanisms by which these proteins impact vascular function remain largely undefined. The matricellular protein lipocalin-7 (LCN7) is found throughout vascular microenvironments, and circumstantial evidence suggests that LCN7 may be an important regulator of angiogenesis. Therefore, we hypothesized that LCN7 may be an important regulator of vascular function. METHODOLOGY AND PRINCIPAL FINDINGS: To test this hypothesis, we examined the effect of LCN7 overexpression, recombinant protein and gene knockdown in a series of in vitro and in vivo models of angiogenesis. We found that overexpression of LCN7 in MB114 and SVEC murine endothelial cell lines or administration of highly purified recombinant LCN7 protein increased endothelial cell invasion. Similarly, LCN7 increased angiogenic sprouting from quiescent endothelial cell monolayers and ex vivo aortic rings. Moreover, LCN7 increased endothelial cell sensitivity to TGF-β but did not affect sensitivity to other pro-angiogenic growth factors including bFGF and VEGF. Finally, morpholino based knockdown of LCN7 in zebrafish embryos specifically inhibited angiogenic sprouting but did not affect vasculogenesis within injected embryos. CONCLUSIONS AND SIGNIFICANCE: No functional analysis has previously been performed to elucidate the function of LCN7 in vascular or other cellular processes. Collectively, our results show for the first time that LCN7 is an important pro-angiogenic matricellular protein of vascular microenvironments.
Genes / Markers
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
y1TgTransgenic Insertion
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    Human Disease / Model
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    Sequence Targeting Reagents
    Target Reagent Reagent Type
    tinagl1MO1-tinagl1MRPHLNO
    tp53MO4-tp53MRPHLNO
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    Fish
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    Orthology
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    tinagl1
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    Engineered Foreign Genes
    Marker Marker Type Name
    EGFPEFGEGFP
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    Mapping
    No data available