Loss of periostin function impairs ligament fibroblast activity and facilitates ROS-mediated cellular senescence

FASEB J. 2024 Aug 31;38(16):e23862. doi: 10.1096/fj.202302615RR.

Abstract

Anterior cruciate ligament (ACL) injuries pose a significant challenge due to their limited healing potential, often resulting in premature arthritis. The factors and mechanisms contributing to this inadequate healing process remain elusive. During the acute phase of injury, ACL tissues express elevated periostin levels that decline over time. The functional significance of periostin in ligament biology remains understudied. In this study, we investigated the functional and mechanistic implications of periostin deficiency in ACL biology, utilizing ligament fibroblasts derived from patients and a murine model of ACL rupture. Our investigations unveiled that periostin knockdown compromised fibroblast growth characteristics, hindered the egress of progenitor cells from explants, and arrested cell-cycle progression, resulting in the accumulation of cells in the G0/G1 phase and moderate apoptosis. Concurrently, a significant reduction in the expression of cell-cycle and matrix-related genes was observed. Moreover, periostin deficiency triggered apoptosis through STAT3Y705/p38MAPK signaling and induced cellular senescence through increased production of reactive oxygen species (ROS). Mechanistically, inhibition of ROS production mitigated cell senescence in these cells. Notably, in vivo data revealed that ACL in Postn-/- mice exhibited a higher tearing frequency than wild-type mice under equivalent loading conditions. Furthermore, injured ACL with silenced periostin expression, achieved through nanoparticle-siRNA complex delivery, displayed an elevated propensity for apoptosis and senescence compared to intact ACL in C57BL/6 mice. Together, our findings underscore the pivotal role of periostin in ACL health, injury, and potential for healing.

Keywords: ACL; ROS; STAT3; cell‐cycle; p16INK4A; p38MAPK.

MeSH terms

  • Animals
  • Anterior Cruciate Ligament Injuries* / metabolism
  • Anterior Cruciate Ligament Injuries* / pathology
  • Anterior Cruciate Ligament* / metabolism
  • Apoptosis
  • Cells, Cultured
  • Cellular Senescence* / physiology
  • Female
  • Fibroblasts* / metabolism
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Periostin* / genetics
  • Periostin* / metabolism
  • Reactive Oxygen Species* / metabolism
  • STAT3 Transcription Factor / metabolism

Substances

  • Periostin
  • POSTN protein, human
  • Postn protein, mouse
  • Reactive Oxygen Species
  • STAT3 Transcription Factor