23 research outputs found

    Biomimicking Fiber Platform with Tunable Stiffness to Study Mechanotransduction Reveals Stiffness Enhances Oligodendrocyte Differentiation but Impedes Myelination through YAP-dependent Regulation

    Get PDF
    A key hallmark of many diseases, especially those in the central nervous system (CNS), is the change in tissue stiffness due to inflammation and scarring. However, how such changes in microenvironment affect the regenerative process remains poorly understood. Here, a biomimicking fiber platform that provides independent variation of fiber structural and intrinsic stiffness is reported. To demonstrate the functionality of these constructs as a mechanotransduction study platform, these substrates are utilized as artificial axons and the effects of axon structural versus intrinsic stiffness on CNS myelination are independently analyzed. While studies have shown that substrate stiffness affects oligodendrocyte differentiation, the effects of mechanical stiffness on the final functional state of oligodendrocyte (i.e., myelination) has not been shown prior to this. Here, it is demonstrated that a stiff mechanical microenvironment impedes oligodendrocyte myelination, independently and distinctively from oligodendrocyte differentiation. Yes-associated protein is identified to be involved in influencing oligodendrocyte myelination through mechanotransduction. The opposing effects on oligodendrocyte differentiation and myelination provide important implications for current work screening for promyelinating drugs, since these efforts have focused mainly on promoting oligodendrocyte differentiation. Thus, the platform may have considerable utility as part of a drug discovery program in identifying molecules that promote both differentiation and myelination

    Designing a composite structure based on resorbable synthetic and natural polymers for anterior cruciate ligament reconstruction

    No full text
    Suite Ă  un accident, les lĂ©sions du ligament croisĂ© antĂ©rieur sont de plus en plus frĂ©quentes devenant un problĂšme de santĂ© publique. En rĂ©ponse Ă  la demande de solutions alternatives aux traitements chirurgicaux actuels, nous avons dĂ©veloppĂ© un renfort ligamentaire en biomatĂ©riaux dĂ©gradables. Pour rĂ©pondre Ă  l'exigence de la rĂ©gĂ©nĂ©ration ligamentaire, ce dernier doit ĂȘtre suffisamment rĂ©sistant pour rĂ©pondre aux contraintes physiologiques du genou, et doit se dĂ©grader tout en permettant la rĂ©gĂ©nĂ©ration d'un nouveau ligament. Nous avons synthĂ©tisĂ© de nouveaux copolymĂšres bloc Ă  base de PLA et de poloxamĂšre ou poloxamine qui ont Ă©tĂ© filĂ©s puis tricotĂ©s pour concevoir un textile tubulaire. Ce textile tubulaire possĂšde des caractĂ©ristiques mĂ©caniques intĂ©ressantes pour le remplacement d'un ligament. En parallĂšle, a Ă©tĂ© dĂ©veloppĂ©e une matrice poreuse Ă  trois dimensions en collagĂšne et glycoaminoglycanes. Cette matrice permet de favoriser l'adhĂ©sion et la prolifĂ©ration cellulaire. Le renfort tricotĂ© associĂ© Ă  la matrice de collagĂšne a Ă©tĂ© implantĂ© in vivo durant 3 mois. A 3 mois, parfaitement intĂ©grĂ©e, la structure composite permet la formation d'un nĂ©o-tissu tout en perdant progressivement ses propriĂ©tĂ©s mĂ©caniques.Following accidents, anterior cruciate ligament (ACL) damages are increasingly becoming a common public health problem. To comply with the demand for alternatives to current surgical treatments, we have developed ligament reinforcement with degradable biomaterials. To meet the requirement of ligament regeneration, ligament reinforcement must be strong enough to support knee physiological strains, and must degrade while allowing the new ligament regeneration. Novel block copolymers PLA- and poloxamer or poloxamine based have been synthesized which were then spun for designing a tubular knitted fabric. The tubular fabric has interesting mechanical characteristics for ligament replacement. In parallel, a collagen and glycosaminoglycans porous three-dimensional matrix has been developed. This matrix is able to promote cell adhesion and proliferation. The knitted reinforcement associated with the collagen matrix has been implanted in vivo for 3 months. Fully integrated, the composite structure allows nĂ©o-tissue formation while gradually losing its mechanical properties after 3 months

    Scaffold-mediated sequential drug/gene delivery to promote nerve regeneration and remyelination following traumatic nerve injuries

    No full text
    Neural tissue regeneration following traumatic injuries is often subpar. As a result, the field of neural tissue engineering has evolved to find therapeutic interventions and has seen promising outcomes. However, robust nerve and myelin regeneration remain elusive. One possible reason may be the fact that tissue regeneration often follows a complex sequence of events in a temporally-controlled manner. Although several other fields of tissue engineering have begun to recognise the importance of delivering two or more biomolecules sequentially for more complete tissue regeneration, such serial delivery of biomolecules in neural tissue engineering remains limited. This review aims to highlight the need for sequential delivery to enhance nerve regeneration and remyelination after traumatic injuries in the central nervous system, using spinal cord injuries as an example. In addition, possible methods to attain temporally-controlled drug/gene delivery are also discussed for effective neural tissue regeneration.NRF (Natl Research Foundation, S’pore)NMRC (Natl Medical Research Council, S’pore)MOH (Min. of Health, S’pore)Accepted versio

    Design of Hybrid Polymer Nanofiber/Collagen Patches Releasing IGF and HGF to Promote Cardiac Regeneration

    No full text
    Cardiovascular diseases are the leading cause of death globally. Myocardial infarction in particular leads to a high rate of mortality, and in the case of survival, to a loss of myocardial functionality due to post-infarction necrosis. This functionality can be restored by cell therapy or biomaterial implantation, and the need for a rapid regeneration has led to the development of bioactive patches, in particular through the incorporation of growth factors (GF). In this work, we designed hybrid patches composed of polymer nanofibers loaded with HGF and IGF and associated with a collagen membrane. Among the different copolymers studied, the polymers and their porogens PLA-Pluronic-PLA + PEG and PCL + Pluronic were selected to encapsulate HGF and IGF. While 89 and 92% of IGF were released in 2 days, HGF was released up to 58% and 50% in 35 days from PLA-Pluronic-PLA + PEG and PCL + Pluronic nanofibers, respectively. We also compared two ways of association for the loaded nanofibers and the collagen membrane, namely a direct deposition of the nanofibers on a moisturized collagen membrane (wet association), or entrapment between collagen layers (sandwich association). The interfacial cohesion and the degradation properties of the patches were evaluated. We also show that the sandwich association decreases the burst release of HGF while increasing the release efficiency. Finally, we show that the patches are cytocompatible and that the presence of collagen and IGF promotes the proliferation of C2C12 myoblast cells for 11 days. Taken together, these results show that these hybrid patches are of interest for cardiac muscle regeneration

    PolymÚres synthétiques dégradables pour la conception de dispositifs médicaux implantables

    No full text
    Le secteur des dispositifs mĂ©dicaux implantables est un secteur des produits de santĂ© en pleine expansion et particuliĂšrement dynamique dans le domaine de la recherche. En effet, pour amĂ©liorer la prise en charge des patients et s’adapter au mieux aux exigences cliniques, les chercheurs du domaine conçoivent de nouveaux types de dispositifs mĂ©dicaux. Pour cela, ils utilisent diffĂ©rentes familles de biomatĂ©riaux prĂ©sentant des caractĂ©ristiques chimiques et physiques trĂšs variĂ©es de façon Ă  proposer aux cliniciens des produits de santĂ© parfaitement adaptĂ©s aux applications biomĂ©dicales. Dans cet article, nous montrons, grĂące Ă  un exemple, comment Ă  partir d’une famille de biomatĂ©riaux (les polymĂšres dĂ©gradables), il est possible de concevoir un dispositif mĂ©dical implantable pour la prise en charge thĂ©rapeutique de la rupture du ligament croisĂ© antĂ©rieur. Les principales Ă©tapes conduisant Ă  la conception d’un renfort ligamentaire total sont dĂ©taillĂ©es dans cette Ă©tude. Elles vont de la synthĂšse et la caractĂ©risation de polymĂšres dĂ©gradables jusqu’à la mise en forme en tricot, en passant par l’étude de l’influence de la stĂ©rilisation sur les propriĂ©tĂ©s mĂ©caniques et la vĂ©rification de la cytocompatibilitĂ©

    Creation of a Stable Nanofibrillar Scaffold Composed of Star-Shaped PLA Network Using Sol-Gel Process during Electrospinning

    No full text
    PLA nanofibers are of great interest in tissue engineering due to their biocompatibility and morphology; moreover, their physical properties can be tailored for long-lasting applications. One of the common and efficient methods to improve polymer properties and slow down their degradation is sol-gel covalent crosslinking. However, this method usually results in the formation of gels or films, which undervalues the advantages of nanofibers. Here, we describe a dual process sol-gel/electrospinning to improve the mechanical properties and stabilize the degradation of PLA scaffolds. For this purpose, we synthesized star-shaped PLAs and functionalized them with triethoxysilylpropyl groups (StarPLA-PTES) to covalently react during nanofibers formation. To achieve this, we evaluated the use of (1) a polymer diluent and (2) different molecular weights of StarPLA on electrospinnability, StarPLA-PTES condensation time and crosslinking efficiency. Our results show that the diluent allowed the fiber formation and reduced the condensation time, while the addition of low-molecular-weight StarPLA-PTES improved the crosslinking degree, resulting in stable matrices even after 6 months of degradation. Additionally, these materials showed biocompatibility and allowed the proliferation of fibroblasts. Overall, these results open the door to the fabrication of scaffolds with enhanced stability and prospective long-term applications

    Investigation on the properties of linear PLA-poloxamer and star PLA-poloxamine copolymers for temporary biomedical applications.

    No full text
    International audienceThe objective of this work was to develop and study newbiodegradable thermoplastics with improvedmechanical properties for potential use as temporary implantable biomaterials. Linear poloxamer and star-shaped poloxamine have been used as macroinitiators for the ring-opening polymerization (ROP) of lactide to yield high molecular weight PLA-based thermoplastic block copolymers. The influence of the nature of the macroinitiator, PLA crystallinity and initial molecular weight on the copolymers properties was investigated by performing a 7-week degradation test in PBS. The evaluation of water uptakes and molecular weights during the degradation pointed out an early hydrolytic degradation of the 100-kg∙mol−1 copolymers compared to the 200-kg∙mol−1 ones (molecular weight decrease of ca. 40% and 20%, respectively). A dramatic loss of tensile mechanical properties was also observed for the 100-kg∙mol−1 copolymers, whereas the 200-kg∙mol−1 copolymers showed stable or even slightly improved properties with Young's moduli around 500 MPa and yield strains around 3% to 4%. Finally, the cytocompatibility of the more stable 200 kg∙mol−1 copolymers was confirmed by murine mesenchymal stem cells (MSCs) culture
    corecore