| Literature DB >> 12514129 |
Maarit Rossi1, Hiroyuki Morita, Raija Sormunen, Sari Airenne, Marjut Kreivi, Ling Wang, Naomi Fukai, Bjorn R Olsen, Karl Tryggvason, Raija Soininen.
Abstract
Mice lacking exon 3 of perlecan (Hspg2) gene were generated by gene targeting. Exon deletion does not alter the expression or the reading frame but causes loss of attachment sites for three heparan sulfate (HS) side chains. Hspg2(Delta 3 / Delta 3) mice are viable and fertile but have small eyes. Apoptosis and leakage of cellular material through the lens capsule are observed in neonatal lenses, and lenses degenerate within 3 weeks of birth. Electron microscopy revealed altered structure of the lens capsule through which cells had formed extensions. No kidney malfunction, such as protein uria, was detected in Hspg2(Delta 3 / Delta 3) mutant mice, nor were ultrastructural changes observed in the glomerular basement membranes (BMs). To achieve further depletion in the HS content of the BMs, Hspg2(Delta 3 / Delta 3) mice were bred with collagen XVIII null mice. Lens defects were more severe in the newborn Col18a1(-/-) x Hspg2(Delta 3 / Delta 3) mice and degeneration proceeded faster than in Hspg2(Delta 3 / Delta 3) mice. The results suggest that in the lens capsule, HS chains have a structural function and are essential in the insulation of the lens from its environment and in regulation of incoming signals.Entities:
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Year: 2003 PMID: 12514129 PMCID: PMC140094 DOI: 10.1093/emboj/cdg019
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598