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• W2109145281 abstract "Laminin-211 is a major constituent of the skeletal muscle basement membrane, exerting its biological functions by binding to cell surface receptors integrin α7β1 and dystroglycan (the latter is part of the dystrophin-glycoprotein complex). The importance of these molecules for normal muscle function is underscored by the fact that their respective deficiency leads to different forms of muscular dystrophy with different severity in humans and animal models. We recently demonstrated that laminin α2 chain and members of the dystrophin-glycoprotein complex have overlapping but non-redundant roles despite being part of the same adhesion complex. To analyse whether laminin-211 and integrin α7 subunit have non-redundant functions we generated mice deficient in laminin α2 chain and integrin α7 subunit (dy(3K)/itga7). We show that lack of both molecules did not exacerbate the severe phenotype of laminin α2-chain deficient animals. They displayed the same weight, survival and dystrophic pattern of muscle biopsy, with similar degree of inflammation and fibrosis. These data suggest that laminin-211 and integrin α7β1 have intersecting roles in skeletal muscle." @default.
• W2109145281 created "2016-06-24" @default.
• W2109145281 creator A5019979103 @default.
• W2109145281 creator A5075320456 @default.
• W2109145281 date "2015-09-10" @default.
• W2109145281 modified "2023-09-25" @default.
• W2109145281 title "Deletion of integrin α7 subunit does not aggravate the phenotype of laminin α2 chain-deficient mice" @default.
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• W2109145281 doi "https://doi.org/10.1038/srep13916" @default.
• W2109145281 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4564817" @default.
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• W2109145281 hasPublicationYear "2015" @default.
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