Alzheimer's disease: An acquired neurodegenerative laminopathy
Author:
Open Access
- 3 May 2016
- journal article
- review article
- Published by Taylor & Francis in Nucleus
- Vol. 7 (3) , 275-283
Abstract
The nucleus is typically depicted as a sphere encircled by a smooth surface of nuclear envelope. For most cell types, this depiction is accurate. In other cell types and in some pathological conditions, however, the smooth nuclear exterior is interrupted by tubular invaginations of the nuclear envelope, often referred to as a “nucleoplasmic reticulum,” into the deep nuclear interior. We have recently reported a significant expansion of the nucleoplasmic reticulum in postmortem human Alzheimer's disease brain tissue. We found that dysfunction of the nucleoskeleton, a lamin-rich meshwork that coats the inner nuclear membrane and associated invaginations, is causal for Alzheimer's disease-related neurodegeneration in vivo. Additionally, we demonstrated that proper function of the nucleoskeleton is required for survival of adult neurons and maintaining genomic architecture. Here, we elaborate on the significance of these findings in regard to pathological states and physiological aging, and discuss cellular causes and consequences of nuclear envelope invagination.Keywords
This publication has 67 references indexed in Scilit:
- Lamin B1 loss is a senescence-associated biomarkerMolecular Biology of the Cell, 2012
- Regulation of prelamin A but not lamin C by miR-9, a brain-specific microRNAProceedings of the National Academy of Sciences, 2012
- Loss of a DNA binding site within the tail of prelamin A contributes to altered heterochromatin anchorage by progerinFEBS Letters, 2010
- Abnormal development of the cerebral cortex and cerebellum in the setting of lamin B2 deficiencyProceedings of the National Academy of Sciences, 2010
- ABC50 Promotes Translation Initiation in Mammalian CellsJournal of Biological Chemistry, 2009
- Lamin B1 controls oxidative stress responses via Oct-1Journal of Cell Biology, 2009
- Phenotype and Course of Hutchinson–Gilford Progeria SyndromeNew England Journal of Medicine, 2008
- Defects in lamin B1 expression or processing affect interphase chromosome position and gene expressionJournal of Cell Biology, 2007
- Sequencing of the Reannotated LMNB2 Gene Reveals Novel Mutations in Patients with Acquired Partial LipodystrophyThe American Journal of Human Genetics, 2006
- Stochastic and genetic factors influence tissue-specific decline in ageing C. elegansNature, 2002