Cell-mediated drug delivery by gingival interdental papilla mesenchymal stromal cells (GinPa-MSCs) loaded with paclitaxel

Anna Teresa Brini, Valentina Coccè, Lorena Maria Ferreira, Chiara Giannasi, G. Cossellu, Aldo Bruno Gianni', Francesca Angiero, Arianna Bonomi, Luisa Pascucci, Maria Laura Falchetti, Emilio Ciusani, G. Bondiolotti, Francesca Sisto, Giulio Alessandri, A. Pessina, Gianpietro Farronato

Research output: Contribution to journalArticle

Abstract

Objective: Gingival tissue is composed of cell types that contribute to the body’s defense against many agents in oral environment, wound healing and tissue regeneration. Thanks to their easy and scarcely invasive withdrawal procedure, interdental papilla provide a good source of mesenchymal stromal cells (GinPa-MSCs). We isolated GinPa-MSCs and verified their ability to uptake/release the anticancer agent Paclitaxel (PTX). Methods: In vitro expanded GinPa-MSCs were characterized for CD markers by FACS, tested for differentiation ability and analyzed by TEM. Their ability to uptake/release PTX was assessed according to a standardized procedure. Results: The CD expression and chondro-adipo-osteo differentiation ability confirmed the mesenchymal feature of GinPa-MSCs. Surprisingly, 28% of GinPa-MSCs expressed CD14 marker and had an impressive pinocytotic activity. GinPa-MSCs were able to take up and release a sufficient amount of PTX to demonstrate effective in vitro activity against pancreatic carcinoma cells, suggesting that the drug was not inactivated. Conclusions: The procedure to obtain MSCs from interdental papilla is less invasive than that used for both bone marrow and adipose tissue, GinPa-MSCs are easy to expand and can be efficiently loaded with PTX. Taken together these qualities suggest that GinPa-MSCs may prove to be a good tool for cell-mediated drug delivery in cancer, particularly if related to stomatognathic system.

Original languageEnglish
Pages (from-to)789-798
Number of pages10
JournalExpert Opinion on Drug Delivery
Volume13
Issue number6
DOIs
Publication statusPublished - 2016

Fingerprint

Gingiva
Paclitaxel
Mesenchymal Stromal Cells
Pharmaceutical Preparations
Stomatognathic System
Antineoplastic Agents
Wound Healing
Adipose Tissue
Regeneration
Bone Marrow
Bone and Bones

Keywords

  • CFPAC-1
  • drug delivery
  • gingival mesenchymal stromal cells
  • paclitaxel

ASJC Scopus subject areas

  • Pharmaceutical Science

Cite this

Cell-mediated drug delivery by gingival interdental papilla mesenchymal stromal cells (GinPa-MSCs) loaded with paclitaxel. / Brini, Anna Teresa; Coccè, Valentina; Ferreira, Lorena Maria; Giannasi, Chiara; Cossellu, G.; Gianni', Aldo Bruno; Angiero, Francesca; Bonomi, Arianna; Pascucci, Luisa; Falchetti, Maria Laura; Ciusani, Emilio; Bondiolotti, G.; Sisto, Francesca; Alessandri, Giulio; Pessina, A.; Farronato, Gianpietro.

In: Expert Opinion on Drug Delivery, Vol. 13, No. 6, 2016, p. 789-798.

Research output: Contribution to journalArticle

Brini, AT, Coccè, V, Ferreira, LM, Giannasi, C, Cossellu, G, Gianni', AB, Angiero, F, Bonomi, A, Pascucci, L, Falchetti, ML, Ciusani, E, Bondiolotti, G, Sisto, F, Alessandri, G, Pessina, A & Farronato, G 2016, 'Cell-mediated drug delivery by gingival interdental papilla mesenchymal stromal cells (GinPa-MSCs) loaded with paclitaxel', Expert Opinion on Drug Delivery, vol. 13, no. 6, pp. 789-798. https://doi.org/10.1517/17425247.2016.1167037
Brini, Anna Teresa ; Coccè, Valentina ; Ferreira, Lorena Maria ; Giannasi, Chiara ; Cossellu, G. ; Gianni', Aldo Bruno ; Angiero, Francesca ; Bonomi, Arianna ; Pascucci, Luisa ; Falchetti, Maria Laura ; Ciusani, Emilio ; Bondiolotti, G. ; Sisto, Francesca ; Alessandri, Giulio ; Pessina, A. ; Farronato, Gianpietro. / Cell-mediated drug delivery by gingival interdental papilla mesenchymal stromal cells (GinPa-MSCs) loaded with paclitaxel. In: Expert Opinion on Drug Delivery. 2016 ; Vol. 13, No. 6. pp. 789-798.
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abstract = "Objective: Gingival tissue is composed of cell types that contribute to the body’s defense against many agents in oral environment, wound healing and tissue regeneration. Thanks to their easy and scarcely invasive withdrawal procedure, interdental papilla provide a good source of mesenchymal stromal cells (GinPa-MSCs). We isolated GinPa-MSCs and verified their ability to uptake/release the anticancer agent Paclitaxel (PTX). Methods: In vitro expanded GinPa-MSCs were characterized for CD markers by FACS, tested for differentiation ability and analyzed by TEM. Their ability to uptake/release PTX was assessed according to a standardized procedure. Results: The CD expression and chondro-adipo-osteo differentiation ability confirmed the mesenchymal feature of GinPa-MSCs. Surprisingly, 28{\%} of GinPa-MSCs expressed CD14 marker and had an impressive pinocytotic activity. GinPa-MSCs were able to take up and release a sufficient amount of PTX to demonstrate effective in vitro activity against pancreatic carcinoma cells, suggesting that the drug was not inactivated. Conclusions: The procedure to obtain MSCs from interdental papilla is less invasive than that used for both bone marrow and adipose tissue, GinPa-MSCs are easy to expand and can be efficiently loaded with PTX. Taken together these qualities suggest that GinPa-MSCs may prove to be a good tool for cell-mediated drug delivery in cancer, particularly if related to stomatognathic system.",
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AU - Brini, Anna Teresa

AU - Coccè, Valentina

AU - Ferreira, Lorena Maria

AU - Giannasi, Chiara

AU - Cossellu, G.

AU - Gianni', Aldo Bruno

AU - Angiero, Francesca

AU - Bonomi, Arianna

AU - Pascucci, Luisa

AU - Falchetti, Maria Laura

AU - Ciusani, Emilio

AU - Bondiolotti, G.

AU - Sisto, Francesca

AU - Alessandri, Giulio

AU - Pessina, A.

AU - Farronato, Gianpietro

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N2 - Objective: Gingival tissue is composed of cell types that contribute to the body’s defense against many agents in oral environment, wound healing and tissue regeneration. Thanks to their easy and scarcely invasive withdrawal procedure, interdental papilla provide a good source of mesenchymal stromal cells (GinPa-MSCs). We isolated GinPa-MSCs and verified their ability to uptake/release the anticancer agent Paclitaxel (PTX). Methods: In vitro expanded GinPa-MSCs were characterized for CD markers by FACS, tested for differentiation ability and analyzed by TEM. Their ability to uptake/release PTX was assessed according to a standardized procedure. Results: The CD expression and chondro-adipo-osteo differentiation ability confirmed the mesenchymal feature of GinPa-MSCs. Surprisingly, 28% of GinPa-MSCs expressed CD14 marker and had an impressive pinocytotic activity. GinPa-MSCs were able to take up and release a sufficient amount of PTX to demonstrate effective in vitro activity against pancreatic carcinoma cells, suggesting that the drug was not inactivated. Conclusions: The procedure to obtain MSCs from interdental papilla is less invasive than that used for both bone marrow and adipose tissue, GinPa-MSCs are easy to expand and can be efficiently loaded with PTX. Taken together these qualities suggest that GinPa-MSCs may prove to be a good tool for cell-mediated drug delivery in cancer, particularly if related to stomatognathic system.

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