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Nuclear lamina assembly in the first cell cycle of rat liver regeneration

The nuclear lamina is a fibrous structure at the nucleoplasmic surface of the inner nuclear membrane. Its assembly state is regulated by phosphorylation of its protein components, the lamins A, B, and C. The isoprenylation of the lamins is essential for their proper membrane anchoring and functional...

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Published in:Journal of cellular physiology 1997-05, Vol.171 (2), p.135-142
Main Authors: Bruscalupi, Giovannella, Di Croce, Luciano, Lamartina, Stefania, Zaccaria, Maria Letizia, Luzzatto, Annarosa Ciofi, Trentalance, Anna
Format: Article
Language:English
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Summary:The nuclear lamina is a fibrous structure at the nucleoplasmic surface of the inner nuclear membrane. Its assembly state is regulated by phosphorylation of its protein components, the lamins A, B, and C. The isoprenylation of the lamins is essential for their proper membrane anchoring and functionality. The content and the membrane association of nuclear lamins and the subcellular localization at light and electron microscopical levels were studied at different times of rat liver regeneration. This model for the good synchrony of the first cell cycle is particularly suited for the study of cell‐cycle‐dependent modifications and is particularly interesting for the increased protein prenylation found in S phase. The biochemical results show an increased lamin content in nuclear proteins in G1 phase and a decreased content in M phase, along with an enhanced cytosolic localization of A and C lamins at later stages. The morphological results show in M phase, also in nondividing cells, a decreased lamin‐like immunoreactivity around the nucleus with an apparent nuclear lamina disassembly. These data emphasize the dynamic organization of nuclear lamina not only in mitosis but also in interphase. The reduction and partial solubilization of nuclear lamina in M phase suggest a reorganization of the nuclear envelope also in those cells that do not appear in mitosis but have replicated their DNA content that will result in a higher degree of polyploidy. J. Cell. Physiol. 171:135–142, 1997. © 1997 Wiley‐Liss, Inc.
ISSN:0021-9541
1097-4652
DOI:10.1002/(SICI)1097-4652(199705)171:2<135::AID-JCP3>3.0.CO;2-P