Force-responsive Zyxin modulation in periodontal ligament cells is regulated by YAP rather than TAZ

Cell Signal. 2020 Aug:72:109662. doi: 10.1016/j.cellsig.2020.109662. Epub 2020 Apr 21.

Abstract

In the context of mechanically induced force transmission, the modification of the actin cytoskeleton through involvement of zyxin is an established concept. However, in cells of the periodontal ligament (PDL), which is physiologically subjected to intermittent mechanical forces, the force-responsive modulation of zyxin and the molecular key players, which orchestrate its cellular regulation, have not yet been elucidated. By employing indirect immunofluorescence and western blotting with different subcellular fractions, we show here in stretch force-exposed human PDL fibroblasts (hPDLFs) that (i) the zyxin protein is modulated, and (ii) its subcellular localization is altered. More importantly, using a pharmacological intervention approach, to inhibit the nuclear presence of the co-transcriptional activator yes-associated protein (YAP), we evidence for the first time that on the molecular level, the cellular abundance of zyxin, among the Thyrotrophic Embryonic Factor (TEF)-binding proteins, is regulated by YAP rather than TAZ. Our findings provide novel insights into the topic how cells of the periodontium and the periodontal ligament in particular respond and may adapt to mechanical forces, and first time identify YAP as the key player of the intracellular regulation of the mechano-sensor and mechano-transducer zyxin in hPDLFs. Moreover, the findings broaden the current knowledge on YAP, since so far, currently only very few YAP-regulated genes have been identified.

Keywords: Periodontal ligament fibroblasts (PDLFs); Strain; TEAD2; YAP/TAZ; Zyxin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 14-3-3 Proteins / metabolism
  • Adaptor Proteins, Signal Transducing / metabolism*
  • Adolescent
  • Biomechanical Phenomena
  • DNA-Binding Proteins / metabolism
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Male
  • Periodontal Ligament / cytology*
  • Stress, Mechanical
  • Subcellular Fractions / metabolism
  • TEA Domain Transcription Factors
  • Transcription Factors / metabolism*
  • Transcriptional Coactivator with PDZ-Binding Motif Proteins
  • Verteporfin / pharmacology
  • YAP-Signaling Proteins
  • Zyxin / metabolism*

Substances

  • 14-3-3 Proteins
  • Adaptor Proteins, Signal Transducing
  • DNA-Binding Proteins
  • Intracellular Signaling Peptides and Proteins
  • TEA Domain Transcription Factors
  • TEAD2 protein, human
  • Transcription Factors
  • Transcriptional Coactivator with PDZ-Binding Motif Proteins
  • WWTR1 protein, human
  • YAP-Signaling Proteins
  • YAP1 protein, human
  • Zyxin
  • Verteporfin