Literature DB >> 17978823

A cell culture model for investigation of Hirano bodies.

Richard C Davis1, Ruth Furukawa, Marcus Fechheimer.   

Abstract

Hirano bodies are paracrystalline F-actin-rich aggregations associated with a variety of conditions including aging, and neurodegenerative diseases. The composition and structure of these inclusions have been described by immunohistochemistry and ultrastructure, respectively. However, studies of the physiological function and dynamics of Hirano bodies have been hindered due to lack of a facile in vitro experimental system. We have developed a model for formation of Hirano bodies in mammalian cell cultures by expression of the carboxy-terminal fragment (CT) of a 34-kDa actin-bundling protein. Expression of the CT protein induces F-actin rearrangement in HEK 293, HeLa, Cos7 cells, neuroblastoma and astrocytic cells, and in primary neurons. We have termed these structures model Hirano bodies, since their composition and ultrastructure is quite similar to that reported in vivo. Model Hirano bodies in cell cultures sometimes appeared to be formed of a number of smaller domains, suggesting that small aggregates are intermediates in the formation of Hirano bodies. Stable lines expressing CT and bearing model Hirano bodies exhibit normal growth, morphology, and motility. This model provides a valuable system for the study of the dynamics of Hirano bodies, and their role in disease processes.

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Year:  2007        PMID: 17978823     DOI: 10.1007/s00401-007-0275-9

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  16 in total

1.  Formation of Hirano bodies after inducible expression of a modified form of an actin-cross-linking protein.

Authors:  Juan F Reyes; Karen Stone; Jeanie Ramos; Andrew Maselli
Journal:  Eukaryot Cell       Date:  2009-04-10

2.  Requirements for Hirano body formation.

Authors:  Paul Griffin; Ruth Furukawa; Cleveland Piggott; Andrew Maselli; Marcus Fechheimer
Journal:  Eukaryot Cell       Date:  2014-03-14

3.  Isolation and characterization of cytoplasmic cofilin-actin rods.

Authors:  Laurie S Minamide; Sankar Maiti; Judith A Boyle; Richard C Davis; Judith A Coppinger; Yunhe Bao; Timothy Y Huang; John Yates; Gary M Bokoch; James R Bamburg
Journal:  J Biol Chem       Date:  2009-12-17       Impact factor: 5.157

4.  Association of AICD and Fe65 with Hirano bodies reduces transcriptional activation and initiation of apoptosis.

Authors:  Sangdeuk Ha; Ruth Furukawa; Marcus Fechheimer
Journal:  Neurobiol Aging       Date:  2010-02-04       Impact factor: 4.673

5.  Autophagy contributes to degradation of Hirano bodies.

Authors:  Dong-Hwan Kim; Richard C Davis; Ruth Furukawa; Marcus Fechheimer
Journal:  Autophagy       Date:  2009-01       Impact factor: 16.016

Review 6.  Dictyostelium discoideum--a model for many reasons.

Authors:  Sarah J Annesley; Paul R Fisher
Journal:  Mol Cell Biochem       Date:  2009-04-22       Impact factor: 3.396

Review 7.  Connecting the dots between tau dysfunction and neurodegeneration.

Authors:  Bess Frost; Jürgen Götz; Mel B Feany
Journal:  Trends Cell Biol       Date:  2014-08-26       Impact factor: 20.808

Review 8.  Cytoskeletal pathologies of Alzheimer disease.

Authors:  James R Bamburg; George S Bloom
Journal:  Cell Motil Cytoskeleton       Date:  2009-08

9.  Mapping cofilin-actin rods in stressed hippocampal slices and the role of cdc42 in amyloid-beta-induced rods.

Authors:  Richard C Davis; Michael T Maloney; Laurie S Minamide; Kevin C Flynn; Matthew A Stonebraker; James R Bamburg
Journal:  J Alzheimers Dis       Date:  2009       Impact factor: 4.472

10.  Model Hirano bodies protect against tau-independent and tau-dependent cell death initiated by the amyloid precursor protein intracellular domain.

Authors:  Matthew Furgerson; Marcus Fechheimer; Ruth Furukawa
Journal:  PLoS One       Date:  2012-09-18       Impact factor: 3.240

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