6533b7dcfe1ef96bd1273482

RESEARCH PRODUCT

Retinol encapsulated into amorphous Ca2+ polyphosphate nanospheres acts synergistically in MC3T3-E1 cells

Emad TolbaHeinz C. SchröderBärbel Diehl-seifertXiaohong WangWerner E.g. Müller

subject

Chemistry PharmaceuticalRetinal bindingPharmaceutical ScienceEndocytosisCollagen Type IMiceCollagen Type IIIchemistry.chemical_compoundPolyphosphatesExtracellularAnimalsTechnology PharmaceuticalMC3T3Particle SizeVitamin ACollagen Type IICell ProliferationDrug CarriersDose-Response Relationship DrugCell growthSkullRetinolDrug Synergism3T3 CellsGeneral MedicineCalcium CompoundsEndocytosisUp-RegulationRetinol-Binding ProteinsRetinol binding proteinCollagen Type IIINanomedicineBiochemistrychemistryBiophysicsNanospheresProtein BindingBiotechnology

description

Both the quality and quantity of collagen, the major structural component of the skin, decrease in aging skin. We succeeded to encapsulate retinol into amorphous inorganic polyphosphate (polyP) nanoparticles together with calcium ions ("aCa-polyP-NP"), under formation of amorphous Ca-polyP/retinol nanospheres ("retinol/aCa-polyP-NS"). The globular nanospheres are not cytotoxic, show an almost uniform size of ≈ 45 nm and have a retinol content of around 25%. Both components of those nanospheres, retinol and the aCa-polyP-NP, if administered together, caused a strong increase in proliferation of mouse calvaria MC3T3 cells. The expressions of collagen types I, II and III genes, but not the expression of collagen type V gene, were significantly enhanced if retinol is added together with aCa-polyP-NP. This synergistic effect was especially pronounced for the expression of the collagen type III gene. We propose that the synergistic effect of the retinol/aCa-polyP-NS on cell growth and collagen type III expression is induced via two routes, first through cellular uptake of the 45 nm nanospheres by clathrin-mediated endocytosis and second through extracellular disintegration of the nanospheres resulting in the release of retinol which is then taken up into the cells after binding to the retinal binding protein receptor.

https://doi.org/10.1016/j.ejpb.2015.04.005