Herein, we present poly(butylene 1,4-cyclohexanedicarboxylate) (PBCE) films characterized by an unpatterned microstructure and a specific hydrophobicity, capable of boosting a drastic cytoskeleton architecture remodeling, culminating with the neuronal-like differentiation of human bone marrow-mesenchymal stem cells (hBM-MSCs). We have used two different filming procedures to prepare the films, solvent casting (PBCE) and compression-moulding (PBCE*). PBCE film had a rough and porous surface with spherulite-like aggregations (Ø = 10–20 µm) and was characterized by a water contact angle = 100◦. PBCE* showed a smooth and continuous surface without voids and visible spherulite-like aggregations and was more hydrophobic (WCA = 110◦). Both surface characteristics were modulated through the copolymerization of different amounts of ether-oxygen-containing co-units into PBCE chemical structure. We showed that only the surface characteristics of PBCE-solvent-casted films steered hBM-MSCs toward a neuronal-like differentiation. hBM-MSCs lost their canonical mesenchymal morphology, acquired a neuronal polarized shape with a long cell protrusion (≥150 µm), expressed neuron-specific class III β-tubulin and microtubule-associated protein 2 neuronal markers, while nestin, a marker of uncommitted stem cells, was drastically silenced. These events were observed as early as 2-days after cell seeding. Of note, the phenomenon was totally absent on PBCE* film, as hBM-MSCs maintained the mesenchymal shape and behavior and did not express neuronal/glial markers.

Morena F., Argentati C., Soccio M., Bicchi I., Luzi F., Torre L., et al. (2020). Unpatterned bioactive poly(Butylene 1,4-cyclohexanedicarboxylate)-based film fast induced neuronal-like differentiation of human bone marrow-mesenchymal stem cells. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 21(23), 1-23 [10.3390/ijms21239274].

Unpatterned bioactive poly(Butylene 1,4-cyclohexanedicarboxylate)-based film fast induced neuronal-like differentiation of human bone marrow-mesenchymal stem cells

Soccio M.;Munari A.;Emiliani C.;Lotti N.
;
Martino S.
2020

Abstract

Herein, we present poly(butylene 1,4-cyclohexanedicarboxylate) (PBCE) films characterized by an unpatterned microstructure and a specific hydrophobicity, capable of boosting a drastic cytoskeleton architecture remodeling, culminating with the neuronal-like differentiation of human bone marrow-mesenchymal stem cells (hBM-MSCs). We have used two different filming procedures to prepare the films, solvent casting (PBCE) and compression-moulding (PBCE*). PBCE film had a rough and porous surface with spherulite-like aggregations (Ø = 10–20 µm) and was characterized by a water contact angle = 100◦. PBCE* showed a smooth and continuous surface without voids and visible spherulite-like aggregations and was more hydrophobic (WCA = 110◦). Both surface characteristics were modulated through the copolymerization of different amounts of ether-oxygen-containing co-units into PBCE chemical structure. We showed that only the surface characteristics of PBCE-solvent-casted films steered hBM-MSCs toward a neuronal-like differentiation. hBM-MSCs lost their canonical mesenchymal morphology, acquired a neuronal polarized shape with a long cell protrusion (≥150 µm), expressed neuron-specific class III β-tubulin and microtubule-associated protein 2 neuronal markers, while nestin, a marker of uncommitted stem cells, was drastically silenced. These events were observed as early as 2-days after cell seeding. Of note, the phenomenon was totally absent on PBCE* film, as hBM-MSCs maintained the mesenchymal shape and behavior and did not express neuronal/glial markers.
2020
Morena F., Argentati C., Soccio M., Bicchi I., Luzi F., Torre L., et al. (2020). Unpatterned bioactive poly(Butylene 1,4-cyclohexanedicarboxylate)-based film fast induced neuronal-like differentiation of human bone marrow-mesenchymal stem cells. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 21(23), 1-23 [10.3390/ijms21239274].
Morena F.; Argentati C.; Soccio M.; Bicchi I.; Luzi F.; Torre L.; Munari A.; Emiliani C.; Gigli M.; Lotti N.; Armentano I.; Martino S.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/797823
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