Extracellular matrix mimics using hyaluronan-based biomaterials

Hyaluronan (HA) is a critical element of the extracellular matrix (ECM). The regulated synthesis and degradation of HA modulates the ECM chemical and physical properties that, in turn, influence cellular behavior. HA triggers signaling pathways associated with the adhesion, proliferation, migration, and differentiation of cells, mediated by its interaction with specific cellular receptors or by tuning the mechanical properties of the ECM. This review summarizes the recent advances on strategies used to mimic the HA present in the ECM to study healthy or pathological cellular behavior. This includes the development of HA-based 2D and 3D in vitro tissue models for the seeding and encapsulation of cells, respectively, and HA particles as carriers for the targeted delivery of therapeutic agents.The authors acknowledge thefinancial support from the European Commission’s H2020 programme, under grantagreements H2020-WIDESPREAD-2014-668983-FORECAST, and H2020-MSCA-RISE-2019-872648-MEPHOS. S.A.acknowledges the Portuguese Foundation for Science and Technology (FCT) for her PhD grant (SFRH/BD/112075/2015)

Experimental determination of the non-extensive entropic parameter qq

We show how to extract the $q$ parameter from experimental data, considering an inhomogeneous magnetic system composed by many Maxwell-Boltzmann homogeneous parts, which after integration over the whole system recover the Tsallis non-extensivity. Analyzing the cluster distribution of La$_{0.7}$Sr$_{0.3}$MnO$_{3}$ manganite, obtained through scanning tunnelling spectroscopy, we measure the $q$ parameter and predict the bulk magnetization with good accuracy. The connection between the Griffiths phase and non-extensivity is also considered. We conclude that the entropic parameter embodies information about the dynamics, the key role to describe complex systems.Comment: Submitted to Phys. Rev. Let

Experimental Determination of Thermal Entanglement in Spin Clusters using Magnetic Susceptibility Measurements

The present work reports an experimental observation of thermal entanglement in a clusterized spin chain formed in the compound Na$_2$Cu$_5$Si$_4$O$_{14}$. The presence of entanglement was investigated through two measured quantities, an Entanglement Witness and the Entanglement of Formation, both derived from the magnetic susceptibility. It was found that pairwise entanglement exists below $\sim 200$ K. Tripartite entanglement was also observed below $\sim 240$ K. A theoretical study of entanglement evolution as a function of applied field and temperature is also presented.Comment: Submited to Phys. Rev.

Wetspun poly-L-(lactic acid)-borosilicate bioactive glass scaffolds for guided bone regeneration

We developed a porous poly-L-lactic acid (PLLA) scaffold compounded with borosilicate bioactive glasses (BBGs) endowing it with bioactive properties. Porous PLLA-BBG fibre mesh scaffolds were successfully prepared by the combination of wet spinning and fibre bonding techniques. Micro-computed tomography (μCT) confirmed that the PLLA-BBG scaffolds containing ≈ 25% of BBGs (w/w) exhibited randomly interconnected porous (58 to 62% of interconnectivity and 53 to 67% of porosity) with mean pore diameters higher that 100 μm. Bioactivity and degradation studies were performed by immersing the scaffolds in simulated body fluid (SBF) and ultrapure water, respectively. The PLLA-BBG scaffolds presented a faster degradation rate with a constant release of inorganic species, which are capable to produce calcium phosphate structures at the surface of the material after 7 days of immersion in SBF (Ca/P ratio of ~ 1.7). Cellular in vitro studies with human osteosarcoma cell line (Saos-2) and human adipose-derived stem cells (hASCs) showed that PLLA-BBGs are not cytotoxic to cells, while demonstrating their capacity to promote cell adhesion and proliferation. Overall, we showed that the proposed scaffolds present a tailored kinetics on the release of inorganic species and controlled biological response under conditions that mimic the bone physiological environment.JSF acknowledges the Portuguese Foundation for Science and Technology (FCT) for his PhD grant BD/73162/2010. This work was partially supported by the European Research Council grant agreement ERC-2012-ADG20120216-321266 - project ComplexiTE

Identification of a Novel Mutation in a Family with Pseudohypoparathyroidism Type 1a

INTRODUCTION: Pseudohypoparathyroidism type 1a is caused by GNAS mutations leading to target organ resistance to multiple hormones rather than parathyroid hormone, resulting not only in hypocalcemia, but also in Albright's hereditary osteodystrophy phenotype. MATERIALS AND METHODS: DNA sequencing of the GNAS gene identified a novel heterozygous mutation in peripheral blood leukocytes in the family presented in this case report. RESULTS: We present a case of a 25-year-old woman with pseudohypoparathyroidism type 1a admitted with seizures, whose family presents an autosomal dominant transmission of a novel heterozygous GNAS mutation (c.524_530+3del). CONCLUSION: Pseudohypoparathyroidism type 1a is mostly caused by inactivating GNAS mutations that have been gradually reported in the literature that lead to a typical and complex clinical phenotype and resistance to multiple hormones. The deletion caused by the mutation identified in the presented case has not been reported previously.info:eu-repo/semantics/publishedVersio