We applied a bottom-up approach to develop biofunctional supramolecular hydrogels from an aromatic glycodipeptide. The self-assembly of the glycopeptide was induced by either temperature manipulation (heating-cooling cycle) or solvent (DMSO to water) switch. The sol-gel transition was salt-triggered in cell culture media and resulted in gels with the same chemical compositions but different mechanical properties. Human adipose derived stem cells (hASCs) cultured on these gels under basal conditions (i.e., without differentiation factors) overexpressed neural markers, such as GFAP, Nestin, MAP2, and βIII-tubulin, confirming the differentiation into neural lineages. The mechanical properties of the gels influenced the number and distribution of the adhered cells. A comparison with gels obtained from the nonglycosylated peptide showed that glycosylation is crucial for the biofunctionality of the hydrogels by capturing and preserving essential growth factors, e.g., FGF-2.

The self-assembly of amyloid-β (Aβ) generates cytotoxic oligomers linked to the onset and progression of Alzheimer’s disease (AD). As many fundamental molecular pathways that control Aβ aggregation are yet to be unraveled, an important strategy to control Aβ cytotoxicity is the development of bioactive synthetic nanotools capable of interacting with the heterogeneous ensemble of Aβ species and remodel them into noncytotoxic forms. Herein, the synthesis of nanosized, functional gallic acid (Ga)-based dendrimers with a precise number of Ga at their surface is described. It is shown that these Ga-terminated dendrimers interact by H-bonding with monomeric/oligomeric Aβ species at their Glu, Ala, and Asp residues, promoting their remodeling into noncytotoxic aggregates in a process controlled by the Ga units. The multivalent presentation of Ga on the dendrimer surface enhances their ability to interact with Aβ, inhibiting the primary and secondary nucleation of Aβ fibrillization and disrupting the Aβ preformed fibrils.

UV radiation is known to induce the premature aging of human skin and to contribute to the occurrence of different skin cancers. High doses of UVA (which is able to penetrate through the epidermis into the dermis) and/or UVB radiation (which only affects the epidermis) lead to cellular oxidative damage compromising the recovery of the normal functions of the cells. This cellular damage is mainly driven by the generation of reactive oxygen species (ROS) that alter the redox status of the intracellular milieu, affecting the cellular metabolic activity, leading to DNA damage, apoptosis and, consequently, to a drastic decrease in the number of live cells, compromising the function of the skin. A series of polyphenolic fractions were extracted from the outer bark (cork) of Quercus suber L., and tested for their capacity to reduce the cellular damage promoted by the ROS produced during UV exposure. This was evaluated after exposing L929 fibroblasts to UV radiation in the presence and absence of the cork extracts. In all the cases the extracts at the concentration of 75 μg ml⁻¹ demonstrated the capacity to preserve cell metabolic activity and their typical morphology, as well as to avoid DNA fragmentation after exposure to UV radiation. We were also able to correlate these findings with the intracellular reduction of ROS species and the presence of higher proportions of castalagin and vescalagin in the extracts. Our data prove that cork is a relevant source of antioxidant compounds able to act in the cellular environment, protecting cells against oxidation, reducing the number of ROS species and limiting the negative impact of UV radiation. These extracts can be further exploited in the preparation of anti-UV formulations for skin protection.