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Laminopathies and the long strange trip from basic cell biology to therapy

期刊

JOURNAL OF CLINICAL INVESTIGATION
卷 119, 期 7, 页码 1825-1836

出版社

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI37679

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资金

  1. NIH [HL76839, CA099506, AR050200, HL086683, AR048997, NS059352, AG02S240]
  2. Muscular Dystrophy Association [MDA4287]
  3. Ellison Medical Research Foundation [AGSS1678]
  4. March of Dimes [FY20071012]

向作者/读者索取更多资源

The main function of the nuclear lamina, an intermediate filament meshwork lying primarily beneath the inner nuclear membrane, is to provide structural scaffolding for the cell nucleus. However, the lamina also serves other functions, such as having a role in chromatin organization, connecting the nucleus to the cytoplasm, gene transcription, and mitosis. In somatic cells, the main protein constituents of the nuclear lamina are lamins A, C, B1, and B2. interest in the nuclear lamins increased dramatically in recent years with the realization that mutations in LMNA, the gene encoding lamins A and C, cause a panoply of human diseases (laminopathies), including muscular dystrophy, cardiomyopathy, partial lipodystrophy, and progeroid syndromes. Here, we review the laminopathies and the long strange trip from basic cell biology to therapeutic approaches for these diseases.

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