Absence of estrogen receptor beta leads to abnormal adipogenesis during early tendon healing by an up-regulation of PPARγ signalling

J Cell Mol Med. 2019 Nov;23(11):7406-7416. doi: 10.1111/jcmm.14604. Epub 2019 Sep 2.

Abstract

Achilles tendon injury is one of the challenges of sports medicine, the aetiology of which remains unknown. For a long time, estrogen receptor β (ERβ) has been known as a regulating factor of the metabolism in many connective tissues, such as bone, muscle and cartilage, but little is known about its role in tendon. Recent studies have implicated ERβ as involved in the process of tendon healing. Tendon-derived stem cells (TDSCs) are getting more and more attention in tendon physiological and pathological process. In this study, we investigated how ERβ played a role in Achilles tendon healing. Achilles tendon injury model was established to analyse how ERβ affected on healing process in vivo. Cell proliferation assay, Western blots, qRT-PCR and immunocytochemistry were performed to investigate the effect of ERβ on TDSCs. Here, we showed that ERβ deletion in mice resulted in inferior gross appearance, histological scores and, most importantly, increased accumulation of adipocytes during the early tendon healing which involved activation of peroxisome proliferator-activated receptor γ (PPARγ) signalling. Furthermore, in vitro results of ours confirmed that the abnormity might be the result of abnormal TDSC adipogenic differentiation which could be partially reversed by the treatment of ERβ agonist LY3201. These data revealed a role of ERβ in Achilles tendon healing for the first time, thereby providing a new target for clinical treatment of Achilles tendon injury.

Keywords: PPARγ signalling; achilles tendon healing; estrogen receptor β; tendon-derived stem cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Achilles Tendon / metabolism*
  • Adipocytes / metabolism
  • Adipogenesis / physiology*
  • Animals
  • Cell Differentiation / physiology
  • Estrogen Receptor beta / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • PPAR gamma / metabolism*
  • Signal Transduction / physiology
  • Stem Cell Transplantation / methods
  • Stem Cells / metabolism
  • Tendon Injuries / metabolism*
  • Transcriptional Activation / physiology
  • Up-Regulation / physiology
  • Wound Healing / physiology*

Substances

  • Estrogen Receptor beta
  • PPAR gamma