Extra Cellular Matrix Deposition and Assembly in Dermis Spheroids

Francesca Rescigno, Laura Ceriotti, Marisa Meloni VitroScreen, In Vitro Innovation Center, Milan, ItalyCorrespondence: Francesca RescignoVitroScreen, In Vitro Innovation Center, via Mosè Bianchi, 103, Milan, 20149, ItalyEmail francesca.rescigno@vitroscreen.comObjective: Dermis spheroids from differe...

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Main Authors: Rescigno F, Ceriotti L, Meloni M
Format: Article
Language:English
Published: Dove Medical Press 2021-07-01
Series:Clinical, Cosmetic and Investigational Dermatology
Subjects:
Online Access:https://www.dovepress.com/extra-cellular-matrix-deposition-and-assembly-in-dermis-spheroids-peer-reviewed-fulltext-article-CCID
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spelling doaj-8b593610fab54bc1ad6d6b577838b2ac2021-07-25T19:23:39ZengDove Medical PressClinical, Cosmetic and Investigational Dermatology1178-70152021-07-01Volume 1493594367170Extra Cellular Matrix Deposition and Assembly in Dermis SpheroidsRescigno FCeriotti LMeloni MFrancesca Rescigno, Laura Ceriotti, Marisa Meloni VitroScreen, In Vitro Innovation Center, Milan, ItalyCorrespondence: Francesca RescignoVitroScreen, In Vitro Innovation Center, via Mosè Bianchi, 103, Milan, 20149, ItalyEmail francesca.rescigno@vitroscreen.comObjective: Dermis spheroids from different donors (40 and 50 years old) were developed from primary fibroblasts to demonstrate their capacity to synthetize and organize the main dermal structural components when cultured in 3D microenvironment, forming endogenous de novo ECM according to their potential metabolic activity.Methods: Dermis spheroids were produced from primary human dermal fibroblasts at early passages in hanging drop culture system. Dermis models were characterized in terms of spheroid diameter, PICP release, collagen III and CD44 expression.Results: An increase of collagen III synthesis (101%) was found in the young donor compared to the old donor (23.5%) after seven days of culture by immunofluorescence. The progressive ECM assembly over the time and dermis maturation was showed by Masson’s trichrome staining and by immunofluorescence for collagen III and CD44; both molecules significantly accumulated in the dermal compartment from day seven to day 10 of culture with a global decrease for both spheroid models after 21 days of culture.Conclusion: Our results showed that specific culture conditions in the 3D scaffold-free microenvironment allowed the physiological and progressive ECM assembly of miniaturized dermis models reflecting phenotypic profile features of “young” and “old” native tissue from which cells were isolated with a potential application to personalized care approaches in dermatological research on aging processes and medicine.Keywords: 3D culture, dermis, scaffold-free spheroids, intrinsic aging, extracellular matrix, tissue remodelinghttps://www.dovepress.com/extra-cellular-matrix-deposition-and-assembly-in-dermis-spheroids-peer-reviewed-fulltext-article-CCID3d culturedermisscaffold-free spheroidsintrinsic agingextracellular matrixtissue remodeling
collection DOAJ
language English
format Article
sources DOAJ
author Rescigno F
Ceriotti L
Meloni M
spellingShingle Rescigno F
Ceriotti L
Meloni M
Extra Cellular Matrix Deposition and Assembly in Dermis Spheroids
Clinical, Cosmetic and Investigational Dermatology
3d culture
dermis
scaffold-free spheroids
intrinsic aging
extracellular matrix
tissue remodeling
author_facet Rescigno F
Ceriotti L
Meloni M
author_sort Rescigno F
title Extra Cellular Matrix Deposition and Assembly in Dermis Spheroids
title_short Extra Cellular Matrix Deposition and Assembly in Dermis Spheroids
title_full Extra Cellular Matrix Deposition and Assembly in Dermis Spheroids
title_fullStr Extra Cellular Matrix Deposition and Assembly in Dermis Spheroids
title_full_unstemmed Extra Cellular Matrix Deposition and Assembly in Dermis Spheroids
title_sort extra cellular matrix deposition and assembly in dermis spheroids
publisher Dove Medical Press
series Clinical, Cosmetic and Investigational Dermatology
issn 1178-7015
publishDate 2021-07-01
description Francesca Rescigno, Laura Ceriotti, Marisa Meloni VitroScreen, In Vitro Innovation Center, Milan, ItalyCorrespondence: Francesca RescignoVitroScreen, In Vitro Innovation Center, via Mosè Bianchi, 103, Milan, 20149, ItalyEmail francesca.rescigno@vitroscreen.comObjective: Dermis spheroids from different donors (40 and 50 years old) were developed from primary fibroblasts to demonstrate their capacity to synthetize and organize the main dermal structural components when cultured in 3D microenvironment, forming endogenous de novo ECM according to their potential metabolic activity.Methods: Dermis spheroids were produced from primary human dermal fibroblasts at early passages in hanging drop culture system. Dermis models were characterized in terms of spheroid diameter, PICP release, collagen III and CD44 expression.Results: An increase of collagen III synthesis (101%) was found in the young donor compared to the old donor (23.5%) after seven days of culture by immunofluorescence. The progressive ECM assembly over the time and dermis maturation was showed by Masson’s trichrome staining and by immunofluorescence for collagen III and CD44; both molecules significantly accumulated in the dermal compartment from day seven to day 10 of culture with a global decrease for both spheroid models after 21 days of culture.Conclusion: Our results showed that specific culture conditions in the 3D scaffold-free microenvironment allowed the physiological and progressive ECM assembly of miniaturized dermis models reflecting phenotypic profile features of “young” and “old” native tissue from which cells were isolated with a potential application to personalized care approaches in dermatological research on aging processes and medicine.Keywords: 3D culture, dermis, scaffold-free spheroids, intrinsic aging, extracellular matrix, tissue remodeling
topic 3d culture
dermis
scaffold-free spheroids
intrinsic aging
extracellular matrix
tissue remodeling
url https://www.dovepress.com/extra-cellular-matrix-deposition-and-assembly-in-dermis-spheroids-peer-reviewed-fulltext-article-CCID
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