HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Col4a1 mutation in mice causes defects in vascular function and low blood pressure associated with reduced red blood cell volume.

Abstract
Collagen type IV is the major structural component of the basement membrane and COL4A1 mutations cause adult small vessel disease, familial porencephaly and hereditary angiopathy with nephropathy aneurysm and cramps (HANAC) syndrome. Here, we show that animals with a Col4a1 missense mutation (Col4a1(+/Raw)) display focal detachment of the endothelium from the media and age-dependent defects in vascular function including a reduced response to nor-epinephrine. Age-dependent hypersensitivity to acetylcholine is abolished by inhibition of nitric oxide synthase (NOS) activity, indicating that Col4a1 mutations affect vasorelaxation mediated by endothelium-derived nitric oxide (NO). These defects are associated with a reduction in basal NOS activity and the development of heightened NO sensitivity of the smooth muscle. The vascular function defects are physiologically relevant as they maintain in part the hypotension in mutant animals, which is primarily associated with a reduced red blood cell volume due to a reduction in red blood cell number, rather than defects in kidney function. To understand the molecular mechanism underlying these vascular defects, we examined the deposition of collagen type IV in the basement membrane, and found it to be defective. Interestingly, this mutation also leads to activation of the unfolded protein response. In summary, our results indicate that mutations in COL4A1 result in a complex vascular phenotype encompassing defects in maintenance of vascular tone, endothelial cell function and blood pressure regulation.
AuthorsTom Van Agtmael, Matthew A Bailey, Ursula Schlötzer-Schrehardt, Eilidh Craigie, Ian J Jackson, David G Brownstein, Ian L Megson, John J Mullins
JournalHuman molecular genetics (Hum Mol Genet) Vol. 19 Issue 6 Pg. 1119-28 (Mar 15 2010) ISSN: 1460-2083 [Electronic] England
PMID20056676 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Collagen Type IV
  • Nitric Oxide
  • Nitric Oxide Synthase
  • Cyclic GMP
Topics
  • Animals
  • Animals, Newborn
  • Blood Vessels (enzymology, pathology, physiopathology, ultrastructure)
  • Cerebral Hemorrhage (blood, complications, pathology, physiopathology)
  • Collagen Type IV (genetics)
  • Cyclic GMP (pharmacology)
  • Endothelial Cells (drug effects, enzymology, pathology)
  • Erythrocyte Volume (physiology)
  • Homeostasis (drug effects)
  • Hypotension (blood, complications, physiopathology)
  • Mice
  • Mice, Inbred C57BL
  • Mice, Mutant Strains
  • Muscle, Smooth, Vascular (drug effects, pathology, physiopathology, ultrastructure)
  • Mutation (genetics)
  • Nitric Oxide (pharmacology)
  • Nitric Oxide Synthase (metabolism)
  • Unfolded Protein Response (drug effects)
  • Vasodilation (drug effects)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: