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α-actinin-4 is essential for maintaining the spreading, motility and contractility of fibroblasts

Shao, H and Wang, JHC and Pollak, MR and Wells, A (2010) α-actinin-4 is essential for maintaining the spreading, motility and contractility of fibroblasts. PLoS ONE, 5 (11).

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Abstract

Background: α-actinins cross-link actin filaments, with this cross-linking activity regulating the formation of focal adhesions, intracellular tension, and cell migration. Most non-muscle cells such as fibroblasts express two isoforms, α-actinin-1 (ACTN1) and α-actinin-4 (ACTN4). The high homology between these two isoforms would suggest redundancy of their function, but recent studies have suggested different regulatory roles. Interestingly, ACTN4 is phosphorylated upon growth factor stimulation, and this loosens its interaction with actin. Methodology/Principal Findings: Using molecular, biochemical and cellular techniques, we probed the cellular functions of ACTN4 in fibroblasts. Knockdown of ACTN4 expression in murine lung fibroblasts significantly impaired cell migration, spreading, adhesion, and proliferation. Surprisingly, knockdown of ACTN4 enhanced cellular compaction and contraction force, and increased cellular and nuclear cross-sectional area. These results, except the increased contractility, are consistent with a putative role of ACTN4 in cytokinesis. For the transcellular tension, knockdown of ACTN4 significantly increased the expression of myosin light chain 2, a element of the contractility machinery. Re-expression of wild type human ACTN4 in ACTN4 knockdown murine lung fibroblasts reverted cell spreading, cellular and nuclear cross-sectional area, and contractility back towards baseline, demonstrating that the defect was due to absence of ACTN4. Significance: These results suggest that ACTN4 is essential for maintaining normal spreading, motility, cellular and nuclear cross-sectional area, and contractility of murine lung fibroblasts by maintaining the balance between transcellular contractility and cell-substratum adhesion. © 2010 Shao et al.


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Details

Item Type: Article
Status: Published
Creators/Authors:
CreatorsEmailPitt UsernameORCID
Shao, H
Wang, JHCwanghc@pitt.eduWANGHC
Pollak, MR
Wells, Aahw6@pitt.eduAHW60000-0002-1637-8150
Contributors:
ContributionContributors NameEmailPitt UsernameORCID
EditorHotchin, Neil A.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Date: 9 December 2010
Date Type: Publication
Journal or Publication Title: PLoS ONE
Volume: 5
Number: 11
DOI or Unique Handle: 10.1371/journal.pone.0013921
Refereed: Yes
MeSH Headings: Actinin--genetics; Actinin--metabolism; Animals; Cell Adhesion; Cell Line; Cell Movement; Cell Proliferation; Cell Shape; Fibroblasts--cytology; Fibroblasts--metabolism; Fibroblasts--ultrastructure; Green Fluorescent Proteins--genetics; Green Fluorescent Proteins--metabolism; Immunoblotting; Lung--cytology; Mice; Mice, Knockout; Microscopy, Electron; Myosin Heavy Chains--genetics; Myosin Heavy Chains--metabolism; Myosin Type II--genetics; Myosin Type II--metabolism; Nonmuscle Myosin Type IIA--genetics; Nonmuscle Myosin Type IIA--metabolism; Nonmuscle Myosin Type IIB--genetics; Nonmuscle Myosin Type IIB--metabolism; Reverse Transcriptase Polymerase Chain Reaction
Other ID: NLM PMC2978680
PubMed Central ID: PMC2978680
PubMed ID: 21085685
Date Deposited: 14 Aug 2012 21:17
Last Modified: 16 Sep 2023 11:55
URI: http://d-scholarship.pitt.edu/id/eprint/13570

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