Role of COL4A1 in small-vessel disease and hemorrhagic stroke

被引:417
作者
Gould, DB
Phalan, FC
van Mil, SE
Sundberg, JP
Vahedi, K
Massin, P
Bousser, MG
Heutink, P
Miner, JH
Tournier-Lasserve, E
John, SWM
机构
[1] Jackson Lab, Bar Harbor, ME 04609 USA
[2] Howard Hughes Med Inst, Bar Harbor, ME USA
[3] VU Univ Med Ctr, Dept Human Genet, Sect Med Genom, Amsterdam, Netherlands
[4] VU Univ, Ctr Neurogenom & Cognit Res, Amsterdam, Netherlands
[5] Hop Lariboisiere, Assistance Publ Hop Paris, Serv Neurol, F-75475 Paris, France
[6] Hop Lariboisiere, Assistance Publ Hop Paris, Serv Ophtalmol, F-75475 Paris, France
[7] Assistance Publ Hop Paris, INSERM, U740, Paris, France
[8] Assistance Publ Hop Paris, Genet Lab, Paris, France
[9] Washington Univ, Sch Med, Div Renal, St Louis, MO 63130 USA
[10] Tufts Univ, Sch Med, Dept Ophthalmol, Boston, MA 02111 USA
关键词
D O I
10.1056/NEJMoa053727
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Small-vessel diseases of the brain underlie 20 to 30 percent of ischemic strokes and a larger proportion of intracerebral hemorrhages. In this report, we show that a mutation in the mouse Col4a1 gene, encoding procollagen type IV alpha l, predisposes both newborn and adult mice to intracerebral hemorrhage. Surgical delivery of mutant mice alleviated birth-associated trauma and hemorrhage. We identified a COL4A1 mutation in a human family with small-vessel disease. We concluded that mutation of COL4A1 may cause a spectrum of cerebrovascular phenotypes and that persons with COL4A1 mutations may be predisposed to hemorrhage, especially after environmental stress.
引用
收藏
页码:1489 / 1496
页数:8
相关论文
共 12 条
[1]  
[Anonymous], 2005, HEART DIS STROKE STA
[2]  
BREEDVELD G, IN PRESS J MED GENET
[3]   Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly [J].
Gould, DB ;
Phalan, FC ;
Breedveld, GJ ;
van Mil, SE ;
Smith, RS ;
Schimenti, JC ;
Aguglia, U ;
van der Knaap, MS ;
Heutink, P ;
John, SWM .
SCIENCE, 2005, 308 (5725) :1167-1171
[4]   Characterization of alpha 1(IV) collagen mutations in Caenorhabditis elegans and the effects of alpha 1 and alpha 2(IV) mutations on type IV collagen distribution [J].
Gupta, MC ;
Graham, PL ;
Kramer, JM .
JOURNAL OF CELL BIOLOGY, 1997, 137 (05) :1185-1196
[5]  
Hawes N L, 1999, Mol Vis, V5, P22
[6]   Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS) [J].
Jen, J ;
Cohen, AH ;
Yue, Q ;
Stout, JT ;
Vinters, HV ;
Nelson, S ;
Baloh, RW .
NEUROLOGY, 1997, 49 (05) :1322-1330
[7]  
KASE CS, 1998, STROKE PATHOPHYSIOLO, P649
[8]   Hereditary porencephaly: clinical and MRI findings in two Dutch families [J].
Mancini, GMS ;
de Coo, IFM ;
Lequin, MH ;
Arts, WF .
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2004, 8 (01) :45-54
[9]   Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3 [J].
Ophoff, RA ;
DeYoung, J ;
Service, SK ;
Joose, M ;
Caffo, NA ;
Sandkuijl, LA ;
Terwindt, GM ;
Haan, J ;
van den Maagdenberg, AMJM ;
Jen, J ;
Baloh, RW ;
Barilla-LaBarca, ML ;
Saccone, NL ;
Atkinson, JP ;
Ferrari, MD ;
Freimer, NB ;
Frants, RR .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (02) :447-453
[10]   Autosomal-dominant familial hematuria with retinal arteriolar tortuosity and contractures: A novel syndrome [J].
Plaisier, E ;
Alamowitch, S ;
Gribouval, O ;
Mougenot, B ;
Gaudric, A ;
Antignac, C ;
Roullet, E ;
Ronco, P .
KIDNEY INTERNATIONAL, 2005, 67 (06) :2354-2360