Autologous Microfragmented Adipose Tissue Reduces the Catabolic and Fibrosis Response in an In Vitro Model of Tendon Cell Inflammation

Background. Mesenchymal stem cells (MSCs) emerged as a promising therapy for tendon pathologies. Microfragmented adipose tissue (μFAT) represents a convenient autologous product for the application of MSC-based therapies in the clinical setting. In the present study, the ability of μFAT to counterac...

Full description

Saved in:
Bibliographic Details
Main Authors: Marco Viganò, Gaia Lugano, Carlotta Perucca Orfei, Alessandra Menon, Enrico Ragni, Alessandra Colombini, Paola De Luca, Pietro Randelli, Laura de Girolamo
Format: Article
Language:English
Published: Wiley 2019-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2019/5620286
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832550987269668864
author Marco Viganò
Gaia Lugano
Carlotta Perucca Orfei
Alessandra Menon
Enrico Ragni
Alessandra Colombini
Paola De Luca
Pietro Randelli
Laura de Girolamo
author_facet Marco Viganò
Gaia Lugano
Carlotta Perucca Orfei
Alessandra Menon
Enrico Ragni
Alessandra Colombini
Paola De Luca
Pietro Randelli
Laura de Girolamo
author_sort Marco Viganò
collection DOAJ
description Background. Mesenchymal stem cells (MSCs) emerged as a promising therapy for tendon pathologies. Microfragmented adipose tissue (μFAT) represents a convenient autologous product for the application of MSC-based therapies in the clinical setting. In the present study, the ability of μFAT to counteract inflammatory processes induced by IL-1β on human tendon cells (TCs) was evaluated. Methods. Cell viability and proliferation were evaluated after 48 hours of transwell coculture of TCs and autologous μFAT in the presence or absence of IL-1β. Gene expression of scleraxis, collagen type I and type III, metalloproteinases-1 and -3, and cyclooxygenase-2 was evaluated by real-time RT-PCR. The content of VEGF, IL-1Ra, TNFα, and IL-6 was evaluated by ELISA. Results. IL-1β-treated TCs showed augmented collagen type III, metalloproteases, and cyclooxygenase-2 expression. μFAT was able to reduce the expression of collagen type III and metalloproteases-1 in a significant manner, and at the same time, it enhanced the production of VEGF, IL-1Ra, and IL-6. Conclusions. In this in vitro model of tendon cell inflammation, the paracrine action of μFAT, exerted by anti-inflammatory molecules and growth factors, was able to inhibit the expression of fibrosis and catabolic markers. Then, these results suggest that the application of μFAT may represent an effective conservative or adjuvant therapy for the treatment of tendon disorders.
format Article
id doaj-art-83f5b62cda6c48b08bf3ea6f9f00a476
institution Kabale University
issn 1687-966X
1687-9678
language English
publishDate 2019-01-01
publisher Wiley
record_format Article
series Stem Cells International
spelling doaj-art-83f5b62cda6c48b08bf3ea6f9f00a4762025-02-03T06:05:19ZengWileyStem Cells International1687-966X1687-96782019-01-01201910.1155/2019/56202865620286Autologous Microfragmented Adipose Tissue Reduces the Catabolic and Fibrosis Response in an In Vitro Model of Tendon Cell InflammationMarco Viganò0Gaia Lugano1Carlotta Perucca Orfei2Alessandra Menon3Enrico Ragni4Alessandra Colombini5Paola De Luca6Pietro Randelli7Laura de Girolamo8Orthopedics Biotechnology Lab, IRCCS Istituto Ortopedico Galeazzi, Milan, ItalyOrthopedics Biotechnology Lab, IRCCS Istituto Ortopedico Galeazzi, Milan, ItalyOrthopedics Biotechnology Lab, IRCCS Istituto Ortopedico Galeazzi, Milan, ItalyLaboratory of Applied Biomechanics, Department of Biomedical Sciences for Health, Università degli Studi di Milano, Via Mangiagalli 31, 20133 Milan, ItalyOrthopedics Biotechnology Lab, IRCCS Istituto Ortopedico Galeazzi, Milan, ItalyOrthopedics Biotechnology Lab, IRCCS Istituto Ortopedico Galeazzi, Milan, ItalyOrthopedics Biotechnology Lab, IRCCS Istituto Ortopedico Galeazzi, Milan, ItalyLaboratory of Applied Biomechanics, Department of Biomedical Sciences for Health, Università degli Studi di Milano, Via Mangiagalli 31, 20133 Milan, ItalyOrthopedics Biotechnology Lab, IRCCS Istituto Ortopedico Galeazzi, Milan, ItalyBackground. Mesenchymal stem cells (MSCs) emerged as a promising therapy for tendon pathologies. Microfragmented adipose tissue (μFAT) represents a convenient autologous product for the application of MSC-based therapies in the clinical setting. In the present study, the ability of μFAT to counteract inflammatory processes induced by IL-1β on human tendon cells (TCs) was evaluated. Methods. Cell viability and proliferation were evaluated after 48 hours of transwell coculture of TCs and autologous μFAT in the presence or absence of IL-1β. Gene expression of scleraxis, collagen type I and type III, metalloproteinases-1 and -3, and cyclooxygenase-2 was evaluated by real-time RT-PCR. The content of VEGF, IL-1Ra, TNFα, and IL-6 was evaluated by ELISA. Results. IL-1β-treated TCs showed augmented collagen type III, metalloproteases, and cyclooxygenase-2 expression. μFAT was able to reduce the expression of collagen type III and metalloproteases-1 in a significant manner, and at the same time, it enhanced the production of VEGF, IL-1Ra, and IL-6. Conclusions. In this in vitro model of tendon cell inflammation, the paracrine action of μFAT, exerted by anti-inflammatory molecules and growth factors, was able to inhibit the expression of fibrosis and catabolic markers. Then, these results suggest that the application of μFAT may represent an effective conservative or adjuvant therapy for the treatment of tendon disorders.http://dx.doi.org/10.1155/2019/5620286
spellingShingle Marco Viganò
Gaia Lugano
Carlotta Perucca Orfei
Alessandra Menon
Enrico Ragni
Alessandra Colombini
Paola De Luca
Pietro Randelli
Laura de Girolamo
Autologous Microfragmented Adipose Tissue Reduces the Catabolic and Fibrosis Response in an In Vitro Model of Tendon Cell Inflammation
Stem Cells International
title Autologous Microfragmented Adipose Tissue Reduces the Catabolic and Fibrosis Response in an In Vitro Model of Tendon Cell Inflammation
title_full Autologous Microfragmented Adipose Tissue Reduces the Catabolic and Fibrosis Response in an In Vitro Model of Tendon Cell Inflammation
title_fullStr Autologous Microfragmented Adipose Tissue Reduces the Catabolic and Fibrosis Response in an In Vitro Model of Tendon Cell Inflammation
title_full_unstemmed Autologous Microfragmented Adipose Tissue Reduces the Catabolic and Fibrosis Response in an In Vitro Model of Tendon Cell Inflammation
title_short Autologous Microfragmented Adipose Tissue Reduces the Catabolic and Fibrosis Response in an In Vitro Model of Tendon Cell Inflammation
title_sort autologous microfragmented adipose tissue reduces the catabolic and fibrosis response in an in vitro model of tendon cell inflammation
url http://dx.doi.org/10.1155/2019/5620286
work_keys_str_mv AT marcovigano autologousmicrofragmentedadiposetissuereducesthecatabolicandfibrosisresponseinaninvitromodeloftendoncellinflammation
AT gaialugano autologousmicrofragmentedadiposetissuereducesthecatabolicandfibrosisresponseinaninvitromodeloftendoncellinflammation
AT carlottaperuccaorfei autologousmicrofragmentedadiposetissuereducesthecatabolicandfibrosisresponseinaninvitromodeloftendoncellinflammation
AT alessandramenon autologousmicrofragmentedadiposetissuereducesthecatabolicandfibrosisresponseinaninvitromodeloftendoncellinflammation
AT enricoragni autologousmicrofragmentedadiposetissuereducesthecatabolicandfibrosisresponseinaninvitromodeloftendoncellinflammation
AT alessandracolombini autologousmicrofragmentedadiposetissuereducesthecatabolicandfibrosisresponseinaninvitromodeloftendoncellinflammation
AT paoladeluca autologousmicrofragmentedadiposetissuereducesthecatabolicandfibrosisresponseinaninvitromodeloftendoncellinflammation
AT pietrorandelli autologousmicrofragmentedadiposetissuereducesthecatabolicandfibrosisresponseinaninvitromodeloftendoncellinflammation
AT lauradegirolamo autologousmicrofragmentedadiposetissuereducesthecatabolicandfibrosisresponseinaninvitromodeloftendoncellinflammation