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Absence of estrogen receptor beta leads to abnormal adipogenesis during early tendon healing by an up‐regulation of PPARγ signalling
Authors:Xuting Bian  Tianyao Liu  Mei Zhou  Gang He  Yuanyuan Ma  Youxing Shi  Yunjiao Wang  Hong Tang  Xia Kang  Mingyu Yang  Jan‐ ke Gustafsson  Xiaotang Fan  Kanglai Tang
Institution:Xuting Bian,Tianyao Liu,Mei Zhou,Gang He,Yuanyuan Ma,Youxing Shi,Yunjiao Wang,Hong Tang,Xia Kang,Mingyu Yang,Jan‐Åke Gustafsson,Xiaotang Fan,Kanglai Tang
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:achilles tendon healing  estrogen receptor β    PPARγ  signalling  tendon‐derived stem cells
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