betaA3/A1-crystallin in astroglial cells regulates retinal vascular remodeling during development.
Sinha D,
Klise A,
Sergeev Y,
Hose S,
Bhutto IA,
Hackler L Jr,
Malpic-Llanos T,
Samtani S,
Grebe R,
Goldberg MF,
Hejtmancik JF,
Nath A,
Zack DJ,
Fariss RN,
McLeod DS,
Sundin O,
Broman KW,
Lutty GA,
Zigler JS Jr.
Department of Ophthalmology, The Johns Hopkins University School of Medicine, Bunting-Blaustein Cancer Research Building II, 1550 Orleans St., Room 146, Baltimore, MD 21231, USA. Debasish@jhmi.edu
Vascular remodeling is a complex process critical to development of the mature vascular system. Astrocytes are known to be indispensable for initial formation of the retinal vasculature; our studies with the Nuc1 rat provide novel evidence that these cells are also essential in the retinal vascular remodeling process. Nuc1 is a spontaneous mutation in the Sprague-Dawley rat originally characterized by nuclear cataracts in the heterozygote and microphthalmia in the homozygote. We report here that the Nuc1 allele results from mutation of the betaA3/A1-crystallin gene, which in the neural retina is expressed only in astrocytes. We demonstrate striking structural abnormalities in Nuc1 astrocytes with profound effects on the organization of intermediate filaments. While vessels form in the Nuc1 retina, the subsequent remodeling process required to provide a mature vascular network is deficient. Our data implicate betaA3/A1-crystallin as an important regulatory factor mediating vascular patterning and remodeling in the retina.
PMID: 17931883 [PubMed - indexed for MEDLINE]