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POLYLACTIDE-POLYGLYCOLIDE RESORBABLE PLATES STIMULATES ADIPOSE TISSUE-DERIVED STEM CELLS TOWARDS OSTEOBLASTS DIFFERENTIATION

Articolo
Data di Pubblicazione:
2011
Citazione:
POLYLACTIDE-POLYGLYCOLIDE RESORBABLE PLATES STIMULATES ADIPOSE TISSUE-DERIVED STEM CELLS TOWARDS OSTEOBLASTS DIFFERENTIATION / V., Sollazzo; Lucchese, Alessandra; A., Palmieri; I., Zollino; C., Iaccarino; G., Carnevali; F., Pezzetti; G., Brunelli; F., Carinci. - In: INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY. - ISSN 0394-6320. - 24:(2011), pp. 59-64. [10.1177/03946320110240s211]
Abstract:
Polylactide, polyglycolide materials or devices have been utilized routinely during maxillofacial, craniofacial, and orthopaedic reconstructive surgical procedures.(1) These materials combine the benefits of rigid fixation with the advantages of biodegradation, avoiding the need for implant removal and minimizing the risk of other complications.(2) To study how polylactide, polyglycolide acids plates (PLPG plates) can induce osteoblast differentiation and proliferation in mesenchymal stem cells, the expression levels of bone related genes (RUNX2, SP7, ALPL, SPP1, COL1A1, COL3A1 and FOSL1) and mesenchymal stem cells marker (ENG) were measured in adipose derived stem cells (ADSCs) and normal osteoblast (NO) cultivated on PLPG plates after 15 and 30 days of treatment using real time Reverse Transcription-Polymerase Chain Reaction. Significantly differentially expressed genes among ADSCs and NO were SP7, ENG, FOSL1, RUNX, ALPL and SPP1 in the first 15 days of treatment and SP7, ENG FOSL1, COL3A1 COL1A1, SPP1 and ALPL after 30 days. The present study demonstrated that PLPG plates strongly influences the behavior of ADSCs in vitro by enhancing proliferation, differentiation and deposition of matrix.
Tipologia CRIS:
1.1 Articolo in rivista
Elenco autori:
V., Sollazzo; Lucchese, Alessandra; A., Palmieri; I., Zollino; C., Iaccarino; G., Carnevali; F., Pezzetti; G., Brunelli; F., Carinci
Link alla scheda completa:
https://iris.unisr.it/handle/20.500.11768/15478
Pubblicato in:
INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY
Journal
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URL

https://journals.sagepub.com/doi/10.1177/03946320110240S211
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