The Interaction Between Human Rotator Cuff Tendon and Subacromial Bursal Tissue in Co-Culture

Author(s):  
Lisa M. Tamburini ◽  
Benjamin J. Levy ◽  
Mary Beth McCarthy ◽  
Danielle E. Kriscenski ◽  
Mark P. Cote ◽  
...  
2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Chang-Meen Sung ◽  
Ra Jeong Kim ◽  
Young-Sool Hah ◽  
Ji-Yong Gwark ◽  
Hyung Bin Park

Abstract Background Bone mineral density of the humeral head is an independent determining factor for postoperative rotator cuff tendon healing. Bisphosphonates, which are commonly used to treat osteoporosis, have raised concerns regarding their relationships to osteonecrosis of the jaw and to atypical fracture of the femur. In view of the prevalence of rotator cuff tear in osteoporotic elderly people, it is important to determine whether bisphosphonates affect rotator cuff tendon healing. However, no studies have investigated bisphosphonates’ cytotoxicity to human rotator cuff tendon fibroblasts (HRFs) or bisphosphonates’ effects on rotator cuff tendon healing. The purpose of this study was to evaluate the cytotoxicity of alendronate (Ald), a bisphosphonate, and its effects on HRF wound healing. Methods HRFs were obtained from human supraspinatus tendons, using primary cell cultures. The experimental groups were control, 0.1 μM Ald, 1 μM Ald, 10 μM Ald, and 100 μM Ald. Alendronate exposure was for 48 h, except during a cell viability analysis with durations from 1 day to 6 days. The experimental groups were evaluated for cell viability, cell cycle and cell proliferation, type of cell death, caspase activity, and wound-healing ability. Results The following findings regarding the 100 μM Ald group contrasted with those for all the other experimental groups: a significantly lower rate of live cells (p < 0.01), a higher rate of subG1 population, a lower rate of Ki-67 positive cells, higher rates of apoptosis and necrosis, a higher number of cells with DNA fragmentation, higher caspase-3/7 activity (p < 0.001), and a higher number of caspase-3 positive staining cells. In scratch-wound healing analyses of all the experimental groups, all the wounds healed within 48 h, except in the 100 μM Ald group (p < 0.001). Conclusions Low concentrations of alendronate appear to have little effect on HRF viability, proliferation, migration, and wound healing. However, high concentrations are significantly cytotoxic, impairing cellular proliferation, cellular migration, and wound healing in vitro.


2014 ◽  
Vol 23 (5) ◽  
pp. 602-603
Author(s):  
Hidehiro Nakamura ◽  
Masafumi Gotoh ◽  
Hideaki Shibata ◽  
Tomonoshin Kanazawa ◽  
Yasuhiro Mitsui ◽  
...  

2012 ◽  
Vol 21 (4) ◽  
pp. 464-473 ◽  
Author(s):  
Stephan Pauly ◽  
Franka Klatte ◽  
Catrin Strobel ◽  
Gerhard Schmidmaier ◽  
Stefan Greiner ◽  
...  

2016 ◽  
Vol 25 (10) ◽  
pp. 1561-1570 ◽  
Author(s):  
Salma Chaudhury ◽  
Zhidao Xia ◽  
Dipti Thakkar ◽  
Osnat Hakimi ◽  
Andrew J. Carr

2018 ◽  
Vol 21 (1) ◽  
pp. 3-14 ◽  
Author(s):  
Jeong Yong Yoon ◽  
Seung Yeon Lee ◽  
Sue Shin ◽  
Kang Sup Yoon ◽  
Chris Hyunchul Jo

BACKGROUND: Platelet-rich plasma (PRP) stimulates cell proliferation and enhances matrix gene expression and synthesis. However, there have been no comparative study of the PRP effect on the normal and degenerative tenocytes. The purpose of this study was to compare the effect of PRP on tenocytes from normal and degenerative tendon.METHODS: Tendon tissues were obtained from patients undergoing arthroscopic repair (n=9) and from healthy donors (n=3). Tenocytes were cultured with 10% (vol/vol) platelet-poor plasma, PRP activated with calcium, and PRP activated with calcium and thrombin. The total cell number was assessed at days 7 and 14. The expressions of type I and III collagen, decorin, tenascin-C, and scleraxis were evaluated by quantitative real-time reverse transcriptase polymerase chain reaction. The total collagen and glycosaminoglycan (GAG) synthesis was evaluated at days 7 and 14.RESULTS: No differences were observed between the groups at day 7, but cell proliferation was remarkably increased in tenocytes from the degenerative tendon at day 14. In both tenocyte groups, the gene expressions of type I and III collagen were up-regulated. GAG synthesis was greater in the normal tendon, whereas the expressions of decorin and tenascin-C were increased in tenocytes from the degenerative tendon. Tenocytes from the degenerative tendon had higher fold-change of GAG synthesis and a lower collagen III/I ratio than normal tenocytes.CONCLUSIONS: PRP promoted the cell proliferation and enhanced the synthesis of tendon matrix in both groups. PRP has a greater positive effect on cell proliferation, matrix gene expression and synthesis in tenocytes from degenerative tendon.


2014 ◽  
Vol 55 (5-6) ◽  
pp. 397-402 ◽  
Author(s):  
Dipti Thakkar ◽  
Tyler M. Grant ◽  
Osnat Hakimi ◽  
Andrew J. Carr

2002 ◽  
Vol 198 (4) ◽  
pp. 207-214 ◽  
Author(s):  
SHU TAKAHASHI ◽  
MIZUHO NAKAJIMA ◽  
MOTO KOBAYASHI ◽  
IKUKO WAKABAYASHI ◽  
NAOHISA MIYAKOSHI ◽  
...  

2008 ◽  
Vol 17 (1) ◽  
pp. S96-S100 ◽  
Author(s):  
Jonas R. Rudzki ◽  
Ronald S. Adler ◽  
Russell F. Warren ◽  
Warren R. Kadrmas ◽  
Nikhail Verma ◽  
...  

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