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Tendon and ligament regeneration and repair: clinical relevance and developmental paradigm.

TLDR
A greater understanding of the molecular mechanisms involved in T/L development and natural healing, coupled with the capability of producing complex biomaterials to deliver multiple biofactors with high spatiotemporal resolution and specificity, should lead to regenerative procedures that more closely recapitulate T/l morphogenesis.
Abstract
Tendon and ligament (T/L) are dense connective tissues connecting bone to muscle and bone to bone, respectively. Similar to other musculoskeletal tissues, T/L arise from the somitic mesoderm, but they are derived from a recently discovered somitic compartment, the syndetome. The adjacent sclerotome and myotome provide inductive signals to the interposing syndetome, thereby upregulating the expression of the transcription factor Scleraxis, which in turn leads to further tenogenic and ligamentogenic differentiation. These advances in the understanding of T/L development have been sought to provide a knowledge base for improving the healing of T/L injuries, a common clinical challenge due to the intrinsically poor natural healing response. Specifically, the three most common tendon injuries involve tearing of the rotator cuff of the shoulder, the flexor tendon of the hand, and the Achilles tendon. At present, injuries to these tissues are treated by surgical repair and/or conservative approaches, including biophysical modalities such as physical rehabilitation and cryotherapy. Unfortunately, the healing tissue forms fibrovascular scar and possesses inferior mechanical and biochemical properties as compared to native T/L. Therefore, tissue engineers have sought to improve upon the natural healing response by augmenting the injured tissue with cells, scaffolds, bioactive agents, and mechanical stimulation. These strategies show promise, both in vitro and in vivo, for improving T/L healing. However, several challenges remain in restoring full T/L function following injury, including uncertainties over the optimal combination of these biological agents as well how to best deliver tissue engineered elements to the injury site. A greater understanding of the molecular mechanisms involved in T/L development and natural healing, coupled with the capability of producing complex biomaterials to deliver multiple growth factors with high spatiotemporal resolution and specificity, will allow tissue engineers to more closely recapitulate T/L morphogenesis, thereby offering future patients the prospect of T/L regeneration, as opposed to simple tissue repair.

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References
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Journal ArticleDOI

Surgical interventions for treating acute achilles tendon rupture: key findings from a recent cochrane review.

TL;DR: There has been a lack of consensus among orthopaedic surgeons regarding the best method for treating acute Achilles tendon rupture, and the incidence is thought to be increasing.
Journal ArticleDOI

The regulation of phenotype of cultured tenocytes by microgrooved surface structure.

TL;DR: It is confirmed that elongated morphology is essential for tenocytes to keep their phenotype and function and can redifferentiate the dedifferentiated tenocytes by the participation of RhoA/ROCK signaling, and these findings may provide insight into the design of advanced scaffold for tendon engineering.
Journal ArticleDOI

Local administration of insulin-like growth factor-I (IGF-I) stimulates tendon collagen synthesis in humans.

TL;DR: In conclusion, local IGF‐I administration can directly enhance tendon collagen synthesis both within and around the human tendon tissue.
Journal Article

Mechanical force modulates scleraxis expression in bioartificial tendons

TL;DR: The results suggest that mechanical signaling exerts an important influence on the expression of genes which play a role in determining the tendon phenotype, and an improved understanding of biology from which optimized rehabilitation programs can be developed.
Journal ArticleDOI

Quantitative variation in vascular endothelial growth factor mRNA expression during early flexor tendon healing: an investigation in a canine model

TL;DR: This work quantified the temporal accumulation of VEGF mRNA at the repair site of an in vivo canine intrasynovial flexor tendon repair and rehabilitation model by means of quantitative Northern blot analysis, in order to detail a molecular signal involved in the intrinsic angiogenic process that accompanies earlyflexor tendon healing.
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