Ovarian failure is the most common cause of infertility. Although numerous strategies have been proposed, a definitive solution for recovering ovarian functions and restoring fertility is currently unavailable. One innovative alternative may be represented by the development of an “artificial ovary” that could be transplanted in patients for re-establishing reproductive activities. Here, we describe a novel approach for successful repopulation of decellularized ovarian bioscaffolds in vitro. Porcine whole ovaries were subjected to a decellularization protocol that removed the cell compartment, while maintaining the macrostructure and microstructure of the original tissue. The obtained bioscaffolds were then repopulated with porcine ovarian cells or with epigenetically erased porcine and human dermal fibroblasts. The results obtained demonstrated that the decellularized extracellular matrix (ECM)-based scaffold may constitute a suitable niche for ex vivo culture of ovarian cells. Furthermore, it was able to properly drive epigenetically erased cell differentiation, fate, and viability. Overall, the method described represents a powerful tool for the in vitro creation of a bioengineered ovary that may constitute a promising solution for hormone and fertility restoration. In addition, it allows for the creation of a suitable 3D platform with useful applications both in toxicological and transplantation studies.

Ovarian decellularized bioscaffolds provide an optimal microenvironment for cell growth and differentiation in vitro / G. Pennarossa, T. De Iorio, F. Gandolfi, T. Brevini. - In: CELLS. - ISSN 2073-4409. - 10:8(2021 Aug 18), pp. 2126.1-2126.19. [10.3390/cells10082126]

Ovarian decellularized bioscaffolds provide an optimal microenvironment for cell growth and differentiation in vitro

G. Pennarossa
Primo
;
T. De Iorio
Secondo
;
F. Gandolfi
Penultimo
;
T. Brevini
Ultimo
2021

Abstract

Ovarian failure is the most common cause of infertility. Although numerous strategies have been proposed, a definitive solution for recovering ovarian functions and restoring fertility is currently unavailable. One innovative alternative may be represented by the development of an “artificial ovary” that could be transplanted in patients for re-establishing reproductive activities. Here, we describe a novel approach for successful repopulation of decellularized ovarian bioscaffolds in vitro. Porcine whole ovaries were subjected to a decellularization protocol that removed the cell compartment, while maintaining the macrostructure and microstructure of the original tissue. The obtained bioscaffolds were then repopulated with porcine ovarian cells or with epigenetically erased porcine and human dermal fibroblasts. The results obtained demonstrated that the decellularized extracellular matrix (ECM)-based scaffold may constitute a suitable niche for ex vivo culture of ovarian cells. Furthermore, it was able to properly drive epigenetically erased cell differentiation, fate, and viability. Overall, the method described represents a powerful tool for the in vitro creation of a bioengineered ovary that may constitute a promising solution for hormone and fertility restoration. In addition, it allows for the creation of a suitable 3D platform with useful applications both in toxicological and transplantation studies.
No
English
bioprosthetic ovary; ECM-based scaffold repopulation; epigenetically erased cells; fibroblasts; human; ovarian reconstruction; porcine; whole-ovary decellularization; animals; cell differentiation; extracellular matrix; female; ovary; swine; tissue engineering; tissue scaffolds
Settore VET/01 - Anatomia degli Animali Domestici
Articolo
Esperti anonimi
Pubblicazione scientifica
   MIND FoodS HUB
   REGIONE LOMBARDIA
18-ago-2021
MDPI
10
8
2126
1
19
19
Pubblicato
Periodico con rilevanza internazionale
scopus
pubmed
crossref
wos
Aderisco
info:eu-repo/semantics/article
Ovarian decellularized bioscaffolds provide an optimal microenvironment for cell growth and differentiation in vitro / G. Pennarossa, T. De Iorio, F. Gandolfi, T. Brevini. - In: CELLS. - ISSN 2073-4409. - 10:8(2021 Aug 18), pp. 2126.1-2126.19. [10.3390/cells10082126]
open
Prodotti della ricerca::01 - Articolo su periodico
4
262
Article (author)
si
G. Pennarossa, T. De Iorio, F. Gandolfi, T. Brevini
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/895526
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