Premium
Adipose‐Derived Stromal Vascular Fraction and Cultured Stromal Cells as Trophic Mediators for Tendon Healing
Author(s) -
Polly Shelley S.,
Nichols Anne E. C.,
Donnini Elle,
Inman Daniel J.,
Scott Timothy J.,
Apple Stephanie M.,
Werre Stephen R.,
Dahlgren Linda A.
Publication year - 2019
Publication title -
journal of orthopaedic research®
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.041
H-Index - 155
eISSN - 1554-527X
pISSN - 0736-0266
DOI - 10.1002/jor.24307
Subject(s) - stromal vascular fraction , adipose tissue , stromal cell , decorin , population , stromal cell derived factor 1 , growth factor , wound healing , adipogenesis , microbiology and biotechnology , medicine , endocrinology , biology , extracellular matrix , immunology , inflammation , proteoglycan , chemokine , receptor , environmental health , cxcr4
Adipose‐derived stromal vascular fraction (SVF) is a heterogeneous population of cells that yields a homogeneous population of plastic‐adherent adipose tissue‐derived stromal cells (ASC) when culture‐expanded. SVF and ASC have been used clinically to improve tendon healing, yet their mechanism of action is not fully elucidated. The objective of this study was to investigate the potential for ASC to act as trophic mediators for tendon healing. Flexor digitorum superficialis tendons and adipose tissue were harvested from adult horses to obtain SVF, ASC, and tenocytes. Growth factor gene expression was quantified in SVF and ASC in serial passages and growth factors were quantified in ASC‐conditioned medium (CM). Microchemotaxis assays were performed using ASC‐CM. Tenocytes were grown in co‐culture with autologous ASC or allogeneic SVF. Gene expression for insulin‐like growth factor 1 (IGF‐1), stromal cell‐derived factor‐1α (SDF‐1α), transforming growth factor‐β1 (TGF‐β1) and TGF‐β3 was significantly higher in SVF compared to ASC. Concentrations were significantly increased in ASC‐CM compared to controls for IGF‐1 (4‐fold) and SDF‐1α (6‐fold). Medium conditioned by ASC induced significant cell migration in a dose‐dependent manner. Gene expression for collagen types I and III, decorin, and cartilage oligomeric matrix protein was modestly, but significantly increased following co‐culture of tenocytes with autologous ASC. Our findings support the ability of SVF and ASC to act as trophic mediators in tendon healing, particularly through chemotaxis, which stands to critically impact the intrinsic healing response. In vivo studies to further delineate the potential for SVF and/or ASC to improve tendon healing are warranted. © 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 37:1429–1439, 2019.