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ErbB2 Is Required for Muscle Spindle and Myoblast Cell Survival

Eran R. AndrechekInstitute for Molecular Biology and Biotechnology, Department of BiologyW. Rod HardySamuel Lunenfeld Research Institute, Mt. Sinai Hospital, TorontoAdele Girgis-GabardoInstitute for Molecular Biology and Biotechnology, Department of BiologyRobert L. PerryInstitute for Molecular Biology and Biotechnology, Department of BiologyRichard ButlerDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, OntarioFrank L. GrahamInstitute for Molecular Biology and Biotechnology, Department of BiologyRonald KahnJoslin Diabetes Center, Department of Medicine, Harvard Medical School, Boston, MassachusettsMichael A. RudnickiWilliam J. MullerDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario
2002en
ABI

Аннотация

Signaling mediated by ErbB2 is thought to play a critical role in numerous developmental processes. However, due to the embryonic lethality associated with the germ line inactivation of erbB2, its role in adult tissues remains largely obscure. Given the expression of ErbB2 at the neuromuscular junction, we have created a muscle-specific knockout to assess its role there. This resulted in viable mice with a progressive defect in proprioception due to loss of muscle spindles. Interestingly, a partial reduction of ErbB2 levels also reduced the number of muscle spindles. Although histological analysis of the muscle revealed an otherwise normal architecture, induction of muscle injury revealed a defect in muscle regeneration. Consistent with these observations, primary myoblasts lacking ErbB2 exhibit extensive apoptosis upon differentiation into myofibers. Taken together, these results illustrate a dual role for ErbB2 in both muscle spindle maintenance and survival of myoblasts.

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