Journal
DEVELOPMENT
Volume 133, Issue 5, Pages 967-975Publisher
COMPANY OF BIOLOGISTS LTD
DOI: 10.1242/dev.02270
Keywords
Pierson syndrome; human; LAMB2; mouse; rat
Categories
Funding
- NIDDK NIH HHS [R01DK064687, R01 DK064687] Funding Source: Medline
- NIGMS NIH HHS [R01 GM060432] Funding Source: Medline
- NINDS NIH HHS [R01NS040759] Funding Source: Medline
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Pierson syndrome is a recently defined disease usually lethal within the first postnatal months and caused by mutations in the gene encoding laminin beta 2 (LAMB2). The hallmarks of Pierson syndrome are congenital nephrotic syndrome accompanied by ocular abnormalities, including microcoria (small pupils), with muscular and neurological developmental defects also present. Lamb2(-/-) mice are a model for Pierson syndrome; they exhibit defects in the kidney glomerular barrier, in the development and organization of the neuromuscular junction, and in the retina. Lamb2(-/-) mice fail to thrive and die very small at 3 weeks of age, but to what extent the kidney and neuromuscular defects each contribute to this severe phenotype has been obscure, though highly relevant to understanding Pierson syndrome. To investigate this, we generated transgenic mouse lines expressing rat laminin beta 2 either in muscle or in glomerular epithelial cells (podocytes) and crossed them onto the Lamb2(-/-) background. Rat beta 2 was confined in skeletal muscle to synapses and myotendinous junctions, and in kidney to the glomerular basement membrane. in transgenic Lamb2(-/-) mice, beta 2 deposition in only glomeruli prevented proteinuria but did not ameliorate the severe phenotype. By contrast, beta 2 expression in only muscle restored synaptic architecture and led to greatly improved health, but the mice died from kidney disease at 1 month. Rescue of both glomeruli and synapses was associated with normal weight gain, fertility and lifespan. We conclude that muscle defects in Lamb2(-/-) mice are responsible for the severe failure to thrive phenotype, and that renal replacement therapy alone will be an inadequate treatment for Pierson syndrome.
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