Fibrillar collagens are the more abundant extracellular proteins. They form a metazoan-specific family, and are highly conserved from sponge to human. Their structural and physiological properties have been successfully used in the food, cosmetic, and pharmaceutical industries. On the other hand, the increase of jellyfish has led us to consider this marine animal as a natural product for food and medicine. Here, we have tested different Mediterranean jellyfish species in order to investigate the economic potential of their collagens. We have studied different methods of collagen purification (tissues and experimental procedures). The best collagen yield was obtained using Rhizostoma pulmo oral arms and the pepsin extraction method (2–10 mg collagen/g of wet tissue). Although a significant yield was obtained with Cotylorhiza tuberculata (0.45 mg/g), R. pulmo was used for further experiments, this jellyfish being considered as harmless to humans and being an abundant source of material. Then, we compared the biological properties of R. pulmo collagen with mammalian fibrillar collagens in cell cytotoxicity assays and cell adhesion. There was no statistical difference in cytotoxicity (p > 0.05) between R. pulmo collagen and rat type I collagen. However, since heparin inhibits cell adhesion to jellyfish-native collagen by 55%, the main difference is that heparan sulfate proteoglycans could be preferentially involved in fibroblast and osteoblast adhesion to jellyfish collagens. Our data confirm the broad harmlessness of jellyfish collagens, and their biological effect on human cells that are similar to that of mammalian type I collagen. Given the bioavailability of jellyfish collagen and its biological properties, this marine material is thus a good candidate for replacing bovine or human collagens in selected biomedical applications.
La présente étude révèle les résultats du programme de recherche financé « Espérance de vie scolaire et handicap – EVS-H ». La visée de ce programme est d’évaluer l’espérance de vie scolaire et les trajectoires de scolarisation d’une population de 197 enfants nés vivants porteurs de malformations congénitales susceptibles de générer des problèmes de santé ou pouvant les mettre en situation fonctionnelle de handicap (tels que troubles moteurs, cognitifs, sensoriels ou encore neuro-développementaux). Ces enfants étaient en âge d’inscription en école primaire quand la loi de février 2005 pour l’égalité des droits et des chances, la participation et la citoyenneté des personnes handicapées a été promulguée. Cette étude amène au constat que L’EVS mesurée en milieu ordinaire et en milieu médico-hospitalier est similaire aux résultats nationaux mais elle est nettement plus basse pour l’EVS calculée dans le milieu ordinaire uniquement. L’article discute les différents résultats permettant ce constat dans la perspective de l’éducation inclusive.
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