Cargando…

Osteogenic and Chondrogenic Potential of the Supramolecular Aggregate T-LysYal®

Hard tissue regeneration represents a challenge for the Regenerative Medicine and Mesenchymal stem cells (MSCs) could be a successful therapeutic strategy. T-LysYal® (T-Lys), a new derivative of Hyaluronic Acid (HA) possessing a superior stability, has already been proved efficient in repairing corn...

Descripción completa

Detalles Bibliográficos
Autores principales: Di Benedetto, Adriana, Posa, Francesca, Marazzi, Mario, Kalemaj, Zamira, Grassi, Roberta, Lo Muzio, Lorenzo, Comite, Mariasevera Di, Cavalcanti-Adam, Elisabetta Ada, Grassi, Felice Roberto, Mori, Giorgio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214626/
https://www.ncbi.nlm.nih.gov/pubmed/32431670
http://dx.doi.org/10.3389/fendo.2020.00285
_version_ 1783532006540312576
author Di Benedetto, Adriana
Posa, Francesca
Marazzi, Mario
Kalemaj, Zamira
Grassi, Roberta
Lo Muzio, Lorenzo
Comite, Mariasevera Di
Cavalcanti-Adam, Elisabetta Ada
Grassi, Felice Roberto
Mori, Giorgio
author_facet Di Benedetto, Adriana
Posa, Francesca
Marazzi, Mario
Kalemaj, Zamira
Grassi, Roberta
Lo Muzio, Lorenzo
Comite, Mariasevera Di
Cavalcanti-Adam, Elisabetta Ada
Grassi, Felice Roberto
Mori, Giorgio
author_sort Di Benedetto, Adriana
collection PubMed
description Hard tissue regeneration represents a challenge for the Regenerative Medicine and Mesenchymal stem cells (MSCs) could be a successful therapeutic strategy. T-LysYal® (T-Lys), a new derivative of Hyaluronic Acid (HA) possessing a superior stability, has already been proved efficient in repairing corneal epithelial cells damaged by dry conditions in vitro. We investigated the regenerative potential of T-Lys in the hard tissues bone and cartilage. We have previously demonstrated that cells isolated from the tooth germ, Dental Bud Stem Cells (DBSCs), differentiate into osteoblast-like cells, representing a promising source of MSCs for bone regeneration. Herewith, we show that T-Lys treatment stimulates the expression of typical osteoblastic markers, such as Runx-2, Collagen I (Col1) and Alkaline Phosphatase (ALP), determining a higher production of mineralized matrix nodules. In addition, we found that T-Lys treatment positively affects α(V)β(3) integrin expression, key integrin in the osteoblastic commitment, leading to the formation of focal adhesions (FAs). The efficacy of T-Lys was also tested on chondrogenic differentiation starting from human articular chondrocytes (HACs) resulting in an increase of differentiation markers and cell number.
format Online
Article
Text
id pubmed-7214626
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-72146262020-05-19 Osteogenic and Chondrogenic Potential of the Supramolecular Aggregate T-LysYal® Di Benedetto, Adriana Posa, Francesca Marazzi, Mario Kalemaj, Zamira Grassi, Roberta Lo Muzio, Lorenzo Comite, Mariasevera Di Cavalcanti-Adam, Elisabetta Ada Grassi, Felice Roberto Mori, Giorgio Front Endocrinol (Lausanne) Endocrinology Hard tissue regeneration represents a challenge for the Regenerative Medicine and Mesenchymal stem cells (MSCs) could be a successful therapeutic strategy. T-LysYal® (T-Lys), a new derivative of Hyaluronic Acid (HA) possessing a superior stability, has already been proved efficient in repairing corneal epithelial cells damaged by dry conditions in vitro. We investigated the regenerative potential of T-Lys in the hard tissues bone and cartilage. We have previously demonstrated that cells isolated from the tooth germ, Dental Bud Stem Cells (DBSCs), differentiate into osteoblast-like cells, representing a promising source of MSCs for bone regeneration. Herewith, we show that T-Lys treatment stimulates the expression of typical osteoblastic markers, such as Runx-2, Collagen I (Col1) and Alkaline Phosphatase (ALP), determining a higher production of mineralized matrix nodules. In addition, we found that T-Lys treatment positively affects α(V)β(3) integrin expression, key integrin in the osteoblastic commitment, leading to the formation of focal adhesions (FAs). The efficacy of T-Lys was also tested on chondrogenic differentiation starting from human articular chondrocytes (HACs) resulting in an increase of differentiation markers and cell number. Frontiers Media S.A. 2020-05-05 /pmc/articles/PMC7214626/ /pubmed/32431670 http://dx.doi.org/10.3389/fendo.2020.00285 Text en Copyright © 2020 Di Benedetto, Posa, Marazzi, Kalemaj, Grassi, Lo Muzio, Comite, Cavalcanti-Adam, Grassi and Mori. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Di Benedetto, Adriana
Posa, Francesca
Marazzi, Mario
Kalemaj, Zamira
Grassi, Roberta
Lo Muzio, Lorenzo
Comite, Mariasevera Di
Cavalcanti-Adam, Elisabetta Ada
Grassi, Felice Roberto
Mori, Giorgio
Osteogenic and Chondrogenic Potential of the Supramolecular Aggregate T-LysYal®
title Osteogenic and Chondrogenic Potential of the Supramolecular Aggregate T-LysYal®
title_full Osteogenic and Chondrogenic Potential of the Supramolecular Aggregate T-LysYal®
title_fullStr Osteogenic and Chondrogenic Potential of the Supramolecular Aggregate T-LysYal®
title_full_unstemmed Osteogenic and Chondrogenic Potential of the Supramolecular Aggregate T-LysYal®
title_short Osteogenic and Chondrogenic Potential of the Supramolecular Aggregate T-LysYal®
title_sort osteogenic and chondrogenic potential of the supramolecular aggregate t-lysyal®
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214626/
https://www.ncbi.nlm.nih.gov/pubmed/32431670
http://dx.doi.org/10.3389/fendo.2020.00285
work_keys_str_mv AT dibenedettoadriana osteogenicandchondrogenicpotentialofthesupramolecularaggregatetlysyal
AT posafrancesca osteogenicandchondrogenicpotentialofthesupramolecularaggregatetlysyal
AT marazzimario osteogenicandchondrogenicpotentialofthesupramolecularaggregatetlysyal
AT kalemajzamira osteogenicandchondrogenicpotentialofthesupramolecularaggregatetlysyal
AT grassiroberta osteogenicandchondrogenicpotentialofthesupramolecularaggregatetlysyal
AT lomuziolorenzo osteogenicandchondrogenicpotentialofthesupramolecularaggregatetlysyal
AT comitemariaseveradi osteogenicandchondrogenicpotentialofthesupramolecularaggregatetlysyal
AT cavalcantiadamelisabettaada osteogenicandchondrogenicpotentialofthesupramolecularaggregatetlysyal
AT grassifeliceroberto osteogenicandchondrogenicpotentialofthesupramolecularaggregatetlysyal
AT morigiorgio osteogenicandchondrogenicpotentialofthesupramolecularaggregatetlysyal