2012
DOI: 10.1155/2012/309187
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Engaging Stem Cells for Customized Tendon Regeneration

Abstract: The need for a consistent therapeutic approach to tendon injury repair is long overdue. Patients with tendon microtears or full ruptures are eligible for a wide range of invasive and non invasive interventions, often subjectively decided by the physician. Surgery produces the best outcomes, and while studies have been conducted to optimize graft constructs and to track outcomes, the data from these studies have been inconclusive on the whole. What has been established is a clear understanding of healthy tendon… Show more

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Cited by 19 publications
(24 citation statements)
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References 124 publications
(97 reference statements)
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“…It is expected that injured vascular capillary networks in the surrounding connective tissue sprout capillary buds along the tubular space of missing tendon. PDGF initiates and guides fibroblast activation, proliferation, and migration [26].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…It is expected that injured vascular capillary networks in the surrounding connective tissue sprout capillary buds along the tubular space of missing tendon. PDGF initiates and guides fibroblast activation, proliferation, and migration [26].…”
Section: Discussionmentioning
confidence: 99%
“…MSCs differentiate into tenocytes (elongated fibroblasts) which are important in collagen synthesis within the extracellular matrix. MSCs produce human foetal tendonspecific matrix components and differentiation factors, which then activate the endogenous regeneration process in tendons [26].…”
Section: Discussionmentioning
confidence: 99%
“…They are processed to remove noncollagen components while retaining the natural collagen structure (predominantly collagen I fibers) and mechanical properties [15]. Materials that have been approved by the Food and Drug Administration (FDA) include Restore™ and CuffPatch (both from SIS), OrthADAPT™ (equine pericardium), Zimmer collagen repair patch and Permacol (both porcine acellular dermal matrix), Bio-BlanketW, TissueMend (bovine dermis and bovine dermal ECM) and GraftJacket (human acellular dermal matrix) [16]. The major drawback of these commercial biological scaffolds is that they have significantly less mechanical properties than normal tendons [17].…”
Section: Pathology and Natural Healingmentioning
confidence: 99%
“…Nondegradable synthetic polymers with FDA approval for tendon repair include polyethylene terephthalate, polypropylene and poly(tetrafluoroethylene) [16]. Several biodegradable synthetic polymers have also obtained FDA approval.…”
Section: Pathology and Natural Healingmentioning
confidence: 99%
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