Journal
EXPERIMENTAL CELL RESEARCH
Volume 316, Issue 6, Pages 992-1001Publisher
ELSEVIER INC
DOI: 10.1016/j.yexcr.2009.12.010
Keywords
Lamin assembly; Internal nuclear matrix; Immunoelectron microscopy; Hepatocytes; Persistent hepatocyte nodules; Fast Fourier transform
Categories
Funding
- Compagnia San Paolo, Italy
Ask authors/readers for more resources
Nuclear lamins are among the more abundant proteins making up the internal nuclear matrix, but very little is known about their structure in the nucleoplasm. Using immunoelectron microscopy, we demonstrate the organization of lamins in the nuclear matrix isolated from rat hepatocytes for the first time. Lamin epitopes are arrayed both in locally ordered clusters and in quasi-regular rows. Fourier filtering of the images demonstrates that the epitopes are placed at the nodes and halfway between the nodes of square or rhombic lattices that are about 50 nm on each side, as well as along rows at regular similar to 25-nm intervals. In addition, we have compared this structure with that of the internal nuclear matrix isolated from persistent hepatocyte nodules. In transformed hepatocytes, the islands of lamin lattice are lost, and only a partial regularity in the rows of gold particles remains. We suggest that orthogonal lattice assembly might be an intrinsic property of lamin molecules, and that the disassembly may be triggered by simple molecular events such as phosphorylation. (C) 2009 Elsevier Inc. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available