Mouse models of MYH9-related disease: mutations in nonmuscle myosin II-A

Yingfan Zhang(National Institutes of Health), Mary Anne Conti(National Institutes of Health), Daniela Malide(National Institutes of Health), Fan Dong(Duke Medical Center), Aibing Wang(National Institutes of Health), Yelena A. Shmist(National Institutes of Health), Chengyu Liu(National Institutes of Health), Patricia M. Zerfas(Office of Research Services), Mathew P. Daniels(National Institutes of Health), Chi‐Chao Chan(National Eye Institute), Elliott D. Kozin(National Institute on Deafness and Other Communication Disorders), Bechara Kachar(National Institute on Deafness and Other Communication Disorders), Michael J. Kelley(Duke Medical Center), Jeffrey B. Kopp(National Institute of Diabetes and Digestive and Kidney Diseases), Robert Adelstein(National Institutes of Health)
Blood
September 9, 2011
Cited by 183Open Access
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Abstract

We have generated 3 mouse lines, each with a different mutation in the nonmuscle myosin II-A gene, Myh9 (R702C, D1424N, and E1841K). Each line develops MYH9-related disease similar to that found in human patients. R702C mutant human cDNA fused with green fluorescent protein was introduced into the first coding exon of Myh9, and D1424N and E1841K mutations were introduced directly into the corresponding exons. Homozygous R702C mice die at embryonic day 10.5-11.5, whereas homozygous D1424N and E1841K mice are viable. All heterozygous and homozygous mutant mice show macrothrombocytopenia with prolonged bleeding times, a defect in clot retraction, and increased extramedullary megakaryocytes. Studies of cultured megakaryocytes and live-cell imaging of megakaryocytes in the BM show that heterozygous R702C megakaryocytes form fewer and shorter proplatelets with less branching and larger buds. The results indicate that disrupted proplatelet formation contributes to the macrothrombocytopenia in mice and most probably in humans. We also observed premature cataract formation, kidney abnormalities, including albuminuria, focal segmental glomerulosclerosis and progressive kidney disease, and mild hearing loss. Our results show that heterozygous mice with mutations in the myosin motor or filament-forming domain manifest similar hematologic, eye, and kidney phenotypes to humans with MYH9-related disease.


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