Abstract
TGF-beta proteins are main regulators of blood vessel development and maintenance. Here, we report an unprecedented link between TGF-beta signaling and arterial hypertension based on the analysis of mice mutant for Emilin1, a cysteine-rich secreted glycoprotein expressed in the vascular tree. Emilin1 knockout animals display increased blood pressure, increased peripheral vascular resistance, and reduced vessel size. Mechanistically, we found that Emilin1 inhibits TGF-beta signaling by binding specifically to the proTGF-beta precursor and preventing its maturation by furin convertases in the extracellular space. In support of these findings, genetic inactivation of Emilin1 causes increased TGF-beta signaling in the vascular wall. Strikingly, high blood pressure observed in Emilin1 mutants is rescued to normal levels upon inactivation of a single TGF-beta1 allele. This study highlights the importance of modulation of TGF-beta availability in the pathogenesis of hypertension.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Arteries / cytology
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Arteries / metabolism
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Blood Pressure / physiology*
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Furin / metabolism
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Gene Dosage
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Genes, Reporter
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Homeostasis*
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Humans
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Hypertension / etiology
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Hypertension / metabolism
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Membrane Glycoproteins / genetics
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Membrane Glycoproteins / metabolism*
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Mice
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Mice, Knockout
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Mice, Transgenic
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Nodal Protein
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Phenotype
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Protein Precursors / metabolism
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Protein Structure, Tertiary
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Receptors, Transforming Growth Factor beta / genetics
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Receptors, Transforming Growth Factor beta / metabolism
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Signal Transduction / physiology*
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Transforming Growth Factor beta / genetics
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Transforming Growth Factor beta / metabolism*
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Xenopus laevis / embryology
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Xenopus laevis / genetics
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Xenopus laevis / metabolism
Substances
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Membrane Glycoproteins
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NODAL protein, human
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Nodal Protein
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Nodal protein, mouse
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Protein Precursors
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Receptors, Transforming Growth Factor beta
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Transforming Growth Factor beta
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elastin microfibril interface located protein
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Furin