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Cartilage matrix is a composite of discrete, but interacting suprastructures, i.e. cartilage fibers with microfibrillar or network-like aggregates and penetrating extrafibrillar proteoglycan matrix. The biomechanical function of the proteoglycan matrix and the collagen fibers are to absorb compressive and tensional loads, respectively. Here, we are focusing on the suprastructural organization of collagen fibrils and the degradation process of their hierarchical organized fiber architecture studied at high resolution at the authentic location within cartilage. We present electron micrographs of the collagenous cores of such fibers obtained by an improved protocol for scanning electron microscopy (SEM). Articular cartilages are permeated by small prototypic fibrils with a homogeneous diameter of 18 ± 5 nm that can align in their D-periodic pattern and merge into larger fibers by lateral association. Interestingly, these fibers have tissue-specific organizations in cartilage. They are twisted ropes in superficial regions of knee joints or assemble into parallel aligned cable-like structures in deeper regions of knee joint- or throughout hip joints articular cartilage. These novel observations contribute to an improved understanding of collagen fiber biogenesis, function, and homeostasis in hyaline cartilage.

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Osteoarthritis (OA) is a chronic degenerative disease of the articular joint that involves both bone and cartilage degenerative changes. An engineered osteochondral tissue within physiological conditions will be of significant utility in understanding the pathogenesis of OA and testing the efficacy of potential disease-modifying OA drugs (DMOADs). In this study, a multichamber bioreactor was fabricated and fitted into a microfluidic base. When the osteochondral construct is inserted, two chambers are formed on either side of the construct (top, chondral; bottom, osseous) that is supplied by different medium streams. These medium conduits are critical to create tissue-specific microenvironments in which chondral and osseous tissues will develop and mature. Human bone marrow stem cell (hBMSCs)-derived constructs were fabricated in situ and cultured within the bioreactor and induced to undergo spatially defined chondrogenic and osteogenic differentiation for 4 weeks in tissue-specific media. We observed tissue specific gene expression and matrix production as well as a basophilic interface suggesting a developing tidemark. Introduction of interleukin-1β (IL-1β) to either the chondral or osseous medium stream induced stronger degradative responses locally as well as in the opposing tissue type. For example, IL-1β treatment of the osseous compartment resulted in a strong catabolic response in the chondral layer as indicated by increased matrix metalloproteinase (MMP) expression and activity, and tissue-specific gene expression. This induction was greater than that seen with IL-1β application to the chondral component directly, indicative of active biochemical communication between the two tissue layers and supporting the osteochondral nature of OA. The microtissue culture system developed here offers novel capabilities for investigating the physiology of osteochondral tissue and pathogenic mechanisms of OA and serving as a high-throughput platform to test potential DMOADS.

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The OActive online training session on “Advanced personalised, multi-scale computer models preventing OsteoArthritis” has come to an end!  We would like to thank the presenters as well as the participants. Our thanks also to the over 200 registered end users.
Training material can be found here.
The video recording is also available on YouTube for those that did not have the chance to attend.  
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The OActive project is organising a training seminar aiming to “Engage end users to the OActive world“, which will be held ONLINE on 29th of May.

The training session will bring together EU and national representatives from:
– the medical care industry
– General public (Individuals, OA patients, elderly, athletes),
– Regulatory authorities (Ministries of health, organisations, orthopaedic associations, etc.)
– Research & education communities

OActive targets patient specific prediction and interventions by using a combination of biomarkers, behavioural modelling, mechanistic computational models, simulations and big data analytics. Scientists from well-established institutes around Europe (including University of Nicosia, LEITAT, KULeuven, Smartex, Liverpool John Moores University, CERTH, University of Patras, RIMED) will give lectures during the training. Participants will be able to raise questions to the panel of experts.

To attend the training please follow the above link to register until 28th of May 2020.

For registration visit here

Participants will be able to attend the meeting for FREE. The training will be organized via an online platform, which will be provided upon registration.

For more information take a look at the agenda: 

 

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Software is present at all levels, at the interface with low level hardware though to the interface with end users, and everything in between.
But the nature of software raises many issues concerning its management, protection and exploitation. This is due to the range of different application areas; its ability to operate globally; its fast rate of development, adaptation and change; and its composite nature. Because we also live in an interconnected world, software needs to manage its interfaces, and to take into consideration formal and de-facto standards, to ensure seamless interoperability.

This webinar will look at some specific issues concerning the protection and exploitation of software, such as the most appropriate IP Rights to use (e.g. patents, database rights, etc), and different exploitation models for design tools, product and services (e.g. Open Source licensing, start-ups, etc).
This webinar is relevant for all those involved with developing and exploiting software tools, products and services; or acquiring or licensing it in; whether they are SMEs, large companies or researchers.

For more information click here

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What was once a science fiction fantasy, virtual reality (VR) technology has evolved and come a long way. Together with augmented reality (AR) technology, these simulations of an alternative environment have been incorporated into rehabilitation treatments. The introduction of head-mounted displays has made VR/AR devices more intuitive and compact, and no longer limited to upper-limb rehabilitation. However, there is still limited evidence supporting the use of VR and AR technology during locomotion, especially regarding the safety and efficacy relating to walking biomechanics. Therefore, the objective of this study is to explore the limitations of such technology through gait analysis. In this study, thirteen participants walked on a treadmill in normal, virtual and augmented versions of the laboratory environment.???

https://tbirehabilitation.wordpress.com/2020/04/02/article-walking-with-head-mounted-virtual-and-augmented-reality-devices-effects-on-position-control-and-gait-biomechanics-full-text-pdf/

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Τhe InSilc  project, one of the projects the OActive Project  is clustering with, is organising a special track (TR22: In silico trials and Clinical Biomechanicsthe) at the 6th Congress of the European Society of Biomechanics in Milan taking place from 12 to 15 July 2020. Check it out https://esbiomech.org/conference/esb2020.

The aim of InSilc is to develop an in-silico clinical trial (ISCT) platform for designing, developing and assessing drug-eluting bioresorbable vascular scaffolds (BVS), by building on the comprehensive biological and biomedical knowledge and advanced modelling approaches to simulate their implantation performance in the individual cardiovascular physiology. Visit 

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Our Partner Ri.MED has just got a paper out in the journal Biofabrication (IF 7.236)
I. Chiesa, C. De Maria, A. Lapomarda, G.M. Fortunato, F. Montemurro, R. Di Gesù, R.S. Tuan, G. Vozzi, R. Gottardi. “Endothelial cells support osteogenesis in an in vitro vascularized bone model developed by 3D bioprinting.” Biofabrication. Published online ahead of printing. Visit link: https://iopscience.iop.org/article/10.1088/1758-5090/ab6a1d

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