Microfragmented adipose tissue is associated with improved ex vivo performance linked to HOXB7 and b-FGF expression.


Journal

Stem cell research & therapy
ISSN: 1757-6512
Titre abrégé: Stem Cell Res Ther
Pays: England
ID NLM: 101527581

Informations de publication

Date de publication:
28 08 2021
Historique:
received: 27 11 2020
accepted: 02 08 2021
entrez: 29 8 2021
pubmed: 30 8 2021
medline: 30 10 2021
Statut: epublish

Résumé

Adipose tissue (AT) has become a source of mesenchymal stromal/stem cells (MSC) for regenerative medicine applications, in particular skeletal disorders. Several enzymatic or mechanical procedures have been proposed to process AT with the aim to isolate cells that can be locally implanted. How AT is processed may impact its properties. Thus, we compared AT processed by centrifugation (C-AT) to microfragmentation (MF-AT). Focusing on MF-AT, we subsequently assessed the impact of synovial fluid (SF) alone on both MF-AT and isolated AT-MSC to better understand their cartilage repair mechanisms. MF-AT and C-AT from the same donors were compared by histology and qRT-PCR immediately after isolation or as ex vivo cultures using a micro-tissue pellet system. The in vitro impact of SF on MF-AT and AT-MSC was assessed by histological staining and molecular analysis. The main AT histological features (i.e., increased extracellular matrix and cellularity) of the freshly isolated or ex vivo-cultured MF-AT persisted compared to C-AT, which rapidly deteriorated during culture. Based on our previous studies of HOX genes in MSC, we investigated the involvement of Homeobox Protein HOX-B7 (HOXB7) and its target basic Fibroblast Growth Factor (bFGF) in the molecular mechanism underlying the improved performance of MF-AT. Indeed, both these biomarkers were more prominent in freshly isolated MF-AT compared to C-AT. SF alone preserved the AT histological features of MF-AT, together with HOXB7 and bFGF expression. Increased cell performance was also observed in isolated AT-MSC after SF treatment concomitant with enhanced HOXB7 expression, although there was no apparent association with bFGF. Our findings show that MF has a positive effect on the maintenance of AT histology and may trigger the expression of trophic factors that improve tissue repair by processed AT.

Identifiants

pubmed: 34454577
doi: 10.1186/s13287-021-02540-1
pii: 10.1186/s13287-021-02540-1
pmc: PMC8399787
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

481

Informations de copyright

© 2021. The Author(s).

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Auteurs

Giulia Casari (G)

Department of Medical and Surgical Sciences for Children and Adults, University-Hospital of Modena and Reggio Emilia, Modena, Italy.
Rigenerand srl, Medolla, Modena, Italy.

Elisa Resca (E)

Technopole Mario Veronesi, Mirandola, Modena, Italy.

Andrea Giorgini (A)

Department of Orthopaedic and Traumatology, University-Hospital of Modena and Reggio Emilia, Modena, Italy.

Olivia Candini (O)

Rigenerand srl, Medolla, Modena, Italy.

Tiziana Petrachi (T)

Technopole Mario Veronesi, Mirandola, Modena, Italy.

Maria Serena Piccinno (MS)

Technopole Mario Veronesi, Mirandola, Modena, Italy.

Elisabetta Manuela Foppiani (EM)

Department of Pediatrics, Emory University, Atlanta, USA.

Lucrezia Pacchioni (L)

Division of Plastic Surgery, Department of General Surgery and Surgical Specialties, University-Hospital of Modena and Reggio Emilia, Modena, Italy.

Marta Starnoni (M)

Division of Plastic Surgery, Department of General Surgery and Surgical Specialties, University-Hospital of Modena and Reggio Emilia, Modena, Italy.

Massimo Pinelli (M)

Division of Plastic Surgery, Department of General Surgery and Surgical Specialties, University-Hospital of Modena and Reggio Emilia, Modena, Italy.

Giorgio De Santis (G)

Division of Plastic Surgery, Department of General Surgery and Surgical Specialties, University-Hospital of Modena and Reggio Emilia, Modena, Italy.

Filippo Selleri (F)

Department of Orthopaedic and Traumatology, University-Hospital of Modena and Reggio Emilia, Modena, Italy.

Fabio Catani (F)

Department of Orthopaedic and Traumatology, University-Hospital of Modena and Reggio Emilia, Modena, Italy.

Massimo Dominici (M)

Department of Medical and Surgical Sciences for Children and Adults, University-Hospital of Modena and Reggio Emilia, Modena, Italy. massimo.dominici@unimore.it.
Rigenerand srl, Medolla, Modena, Italy. massimo.dominici@unimore.it.
Technopole Mario Veronesi, Mirandola, Modena, Italy. massimo.dominici@unimore.it.

Elena Veronesi (E)

Department of Medical and Surgical Sciences for Children and Adults, University-Hospital of Modena and Reggio Emilia, Modena, Italy. elena.veronesi@tpm.bio.
Technopole Mario Veronesi, Mirandola, Modena, Italy. elena.veronesi@tpm.bio.

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Classifications MeSH