| Literature DB >> 10570949 |
T Kawada1, Y Nakatsuru, A Sakamoto, T Koizumi, W S Shin, Y Okai-Matsuo, J Suzuki, Y Uehara, M Nakazawa, H Sato, T Ishikawa, T Toyo-oka.
Abstract
The delta-sarcoglycan (SG) gene is deleted in hamsters with hereditary cardiomyopathies. Immunological analyses of heart before, but not after, the progression of cardiomyopathy (CM) revealed that the BIO 14.6 strain, a model of hypertrophic CM, heterogeneously preserved alpha- and gamma-SG with loss of beta- and delta-SG. In contrast, the TO-2 strain, a model of dilated CM, did not show either SG. Furthermore, in vivo transfer of the full length delta-SG gene to TO-2 hearts expressed all four SGs. Thus, this age- and strain-dependent features suggest a more feasible setting for TO-2 than BIO 14.6 to verify both CM progression and the efficacy of gene therapy.Entities:
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Year: 1999 PMID: 10570949 DOI: 10.1016/s0014-5793(99)01164-3
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124