Extracellular and intracellular mechanisms of mechanotransduction in three-dimensionally embedded rat chondrocytes

PLoS One. 2014 Dec 5;9(12):e114327. doi: 10.1371/journal.pone.0114327. eCollection 2014.

Abstract

Purpose: Articular cartilage homeostasis involves modulation of chondrocyte matrix synthesis in response to mechanical stress (MS). We studied extracellular and intracellular mechanotransduction pathways mediating this response.

Methods: We first confirmed rapid up-regulation of the putative chondro-protective cytokine, interleukin (IL)-4, as an immediate response to MS. We then studied the role of IL-4 by investigating responses to exogenous IL-4 or a specific IL-4 inhibitor, combined with MS. Next we investigated the intracellular second messengers. Since chondrocyte phenotype alters according to the extracellular environment, we characterized the response to mechanotransduction in 3-dimensionally embedded chondrocytes.

Results: Expression of aggrecan and type II collagen was significantly up-regulated by exogenous IL-4 whereas MS-induced matrix synthesis was inhibited by an IL-4 blocker. Further, MS-induced matrix synthesis was completely blocked by a p38 MAPK inhibitor, while it was only partially blocked by inhibitors of other putative second messengers.

Conclusion: IL-4 mediates an extracellular pathway of mechanotransduction, perhaps via an autocrine/paracrine loop, while p38 mediates an intracellular pathway prevalent only in a 3-dimensional environment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autocrine Communication / physiology*
  • Cells, Cultured
  • Chondrocytes / cytology
  • Chondrocytes / metabolism*
  • Extracellular Matrix / metabolism*
  • Interleukin-4 / metabolism
  • Mechanotransduction, Cellular / physiology*
  • Paracrine Communication / physiology*
  • Rats
  • Rats, Wistar

Substances

  • Interleukin-4

Grants and funding

This study was supported by a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (#22500457). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.