Abstract:Ligaments and tendons are fibrous tissues with poor vascularity and limited regeneration capacity. Currently, a ligament/tendon injury often require a surgical procedure using auto-or allografts that present some limitations. These inadequacies combined with the significant economic and health impact have prompted the development of tissue engineering approaches. Several natural and synthetic biodegradable polymers as well as composites, blends and hybrids based on such materials have been used to produce tend… Show more
“…With regard to regeneration of the full-cut tendon defect, it is crucial to utilize the suitable biomaterials to load exogenous growth factors and provide a mechanical support for recruitment of endogenous stem cells or fibroblastic cells, promote natural cell–cell communication, and maintain ECM integrity in the early stage of tendon regeneration 5 , 56 – 58 . Currently available scaffolds (e.g., autografts, allografts, xenografts, and synthetic biomaterials) have several inherent limitations, including donor site morbidity, poor graft integration, high rates of recurrent tearing, and inflammatory responses; these limitations can ultimately cause failed integration of biomechanical and structural tendon regeneration 42 , 59 , 60 . To mimic the native tendon physicochemical architecture, we developed a dynamic diffusion-template self-assembly strategy that allowed orderly assembly of parallel-aligned ECM collagen fibrils.…”
Tendon injuries disrupt the balance between stability and mobility, causing compromised functions and disabilities. The regeneration of mature, functional tendons remains a clinical challenge. Here, we perform transcriptional profiling of tendon developmental processes to show that the extracellular matrix-associated protein periostin (Postn) contributes to the maintenance of tendon stem/progenitor cell (TSPC) functions and promotes tendon regeneration. We show that recombinant periostin (rPOSTN) promotes the proliferation and stemness of TSPCs, and maintains the tenogenic potentials of TSPCs in vitro. We also find that rPOSTN protects TSPCs against functional impairment during long-term passage in vitro. For in vivo tendon formation, we construct a biomimetic parallel-aligned collagen scaffold to facilitate TSPC tenogenesis. Using a rat full-cut Achilles tendon defect model, we demonstrate that scaffolds loaded with rPOSTN promote endogenous TSPC recruitment, tendon regeneration and repair with native-like hierarchically organized collagen fibers. Moreover, newly regenerated tendons show recovery of mechanical properties and locomotion functions.
“…With regard to regeneration of the full-cut tendon defect, it is crucial to utilize the suitable biomaterials to load exogenous growth factors and provide a mechanical support for recruitment of endogenous stem cells or fibroblastic cells, promote natural cell–cell communication, and maintain ECM integrity in the early stage of tendon regeneration 5 , 56 – 58 . Currently available scaffolds (e.g., autografts, allografts, xenografts, and synthetic biomaterials) have several inherent limitations, including donor site morbidity, poor graft integration, high rates of recurrent tearing, and inflammatory responses; these limitations can ultimately cause failed integration of biomechanical and structural tendon regeneration 42 , 59 , 60 . To mimic the native tendon physicochemical architecture, we developed a dynamic diffusion-template self-assembly strategy that allowed orderly assembly of parallel-aligned ECM collagen fibrils.…”
Tendon injuries disrupt the balance between stability and mobility, causing compromised functions and disabilities. The regeneration of mature, functional tendons remains a clinical challenge. Here, we perform transcriptional profiling of tendon developmental processes to show that the extracellular matrix-associated protein periostin (Postn) contributes to the maintenance of tendon stem/progenitor cell (TSPC) functions and promotes tendon regeneration. We show that recombinant periostin (rPOSTN) promotes the proliferation and stemness of TSPCs, and maintains the tenogenic potentials of TSPCs in vitro. We also find that rPOSTN protects TSPCs against functional impairment during long-term passage in vitro. For in vivo tendon formation, we construct a biomimetic parallel-aligned collagen scaffold to facilitate TSPC tenogenesis. Using a rat full-cut Achilles tendon defect model, we demonstrate that scaffolds loaded with rPOSTN promote endogenous TSPC recruitment, tendon regeneration and repair with native-like hierarchically organized collagen fibers. Moreover, newly regenerated tendons show recovery of mechanical properties and locomotion functions.
“…This versatility is attributed to the wide spectrum of physical and chemical properties, ease of fabrication with a wide variety of structures that range from simple mats to complex shapes, and biocompatibility. There are many biomedical applications utilizing polymers, for instance, drug delivery vehicles [ 58 , 59 ], tissue engineering scaffolds [ 60 , 61 ], wound dressing [ 62 , 63 , 64 ], and biomedical sensors [ 65 , 66 ]. Although polymers have suitable bulk properties for some biomedical applications, their surface properties are not appropriate.…”
Section: Modification Of Polymeric Surfaces By Atmospheric Pressurmentioning
Atmospheric plasma treatment is an effective and economical surface treatment technique. The main advantage of this technique is that the bulk properties of the material remain unchanged while the surface properties and biocompatibility are enhanced. Polymers are used in many biomedical applications; such as implants, because of their variable bulk properties. On the other hand, their surface properties are inadequate which demands certain surface treatments including atmospheric pressure plasma treatment. In biomedical applications, surface treatment is important to promote good cell adhesion, proliferation, and growth. This article aim is to give an overview of different atmospheric pressure plasma treatments of polymer surface, and their influence on cell-material interaction with different cell lines.
“…94 However, one of the limitations of synthetic polymers is the lack of bioactive cues, which could be overcome by biological coatings. 59 In one study, galactose was incorporated into electrospun PCL nanofibers, and this composite scaffold resulted in increased meniscal cell attachment and proliferation. 95 Furthermore, Ren In vitro (human primary fibroblasts, primary chondrocytes)…”
The meniscus plays a critical role in maintaining knee joint homeostasis. Injuries to the meniscus, especially considering the limited self-healing capacity of the avascular region, continue to be a challenge and are often treated by (partial) meniscectomy, which has been identified to cause osteoarthritis. Currently, meniscus tissue engineering focuses on providing extracellular matrix (ECM)-mimicking scaffolds to direct the inherent meniscal regeneration process, and it has been found that various stimuli are essential. Numerous bioactive factors present benefits in regulating cell fate, tissue development, and healing, but lack an optimal delivery system. More recently, bioengineers have developed various polymer-based drug delivery systems (PDDSs), which are beneficial in terms of the favorable properties of polymers as well as novel delivery strategies. Engineered PDDSs aim to provide not only an ECM-mimicking microenvironment but also the controlled release of bioactive factors with release profiles tailored according to the biological concerns and properties of the factors. In this review, both different polymers and bioactive factors involved in meniscal regeneration are discussed, as well as potential candidate systems, with examples of recent progress. This article aims to summarize drug delivery strategies in meniscal regeneration, with a focus on novel delivery strategies rather than on specific delivery carriers. The current challenges and future prospects for the structural and functional regeneration of the meniscus are also discussed.
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