Partial Tendon Injury at the Tendon-to-Bone Enthesis Activates Skeletal Stem Cells

Author:

Titan Ashley L12ORCID,Davitt Michael1,Foster Deshka12,Salhotra Ankit1,Menon Siddharth1,Chen Kellen1ORCID,Fahy Evan1,Lopez Michael1,Jones R Ellen1,Baiu Ioana2,Burcham Austin1,Januszyk Michael1,Gurtner Geoffrey12,Fox Paige1,Chan Charles1,Quarto Natalina12,Longaker Michael123

Affiliation:

1. Hagey Laboratory for Pediatric Regenerative Medicine, Department of Surgery, Division of Plastic and Reconstructive Surgery, Stanford University School of Medicine , Stanford, CA , USA

2. Department of Surgery, Stanford University School of Medicine , Stanford, CA , USA

3. Institute of Stem Cell Biology and Regenerative Medicine , Stanford, CA , USA

Abstract

Abstract The tendon enthesis plays a critical role in facilitating movement and reducing stress within joints. Partial enthesis injuries heal in a mechanically inferior manner and never achieve healthy tissue function. The cells responsible for tendon-to-bone healing remain incompletely characterized and their origin is unknown. Here, we evaluated the putative role of mouse skeletal stem cells (mSSCs) in the enthesis after partial-injury. We found that mSSCs were present at elevated levels within the enthesis following injury and that these cells downregulated TGFβ signaling pathway elements at both the RNA and protein levels. Exogenous application of TGFβ post-injury led to a reduced mSSC response and impaired healing, whereas treatment with a TGFβ inhibitor (SB43154) resulted in a more robust mSSC response. Collectively, these data suggest that mSSCs may augment tendon-to-bone healing by dampening the effects of TGFβ signaling within the mSSC niche.

Funder

American College of Surgeons

Stanford Transplant and Tissue Engineering Center of Excellence Fund

NIH

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

Reference71 articles.

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