Skip to Main Content (Press Enter)

Logo UNISR
  • ×
  • Home
  • Persone
  • Pubblicazioni
  • Facoltà
  • Ambiti Di Ricerca

UNIFIND
Logo UNISR

|

UNIFIND

unisr.it
  • ×
  • Home
  • Persone
  • Pubblicazioni
  • Facoltà
  • Ambiti Di Ricerca
  1. Pubblicazioni

Nanoengineered 3D culture substrate enables superior persistence and polyclonal engraftment of genetically engineered hematopoietic stem cells

Articolo
Data di Pubblicazione:
2026
Citazione:
Nanoengineered 3D culture substrate enables superior persistence and polyclonal engraftment of genetically engineered hematopoietic stem cells / Midena, F.; Alessandrini, L.; Conci, C.; Barcella, M.; Gazzo, F.; Jacchetti, E.; Carsana, E.; Benedicenti, F.; Vacca, R.; Della Volpe, L.; Arevalo, S.; Giannetti, K.; Barozzi, D.; Franchino, M.; Zonari, E.; Ferrua, F.; Farina, G.; Brombin, C.; Cugnata, F.; Fiumara, M.; Tavella, T.; Cherubin, L.; Fraschetta, F.; Cerullo, G.; Osellame, R.; Radrizzani, M.; Ferrari, S.; Merelli, I.; Gentner, B.; Scielzo, C.; Brendolan, A.; Naldini, L.; Aiuti, A.; Montini, E.; Raimondi, M. T.; Di Micco, R.. - In: CELL STEM CELL. - ISSN 1934-5909. - 33:2(2026), pp. 217-232.e9. [10.1016/j.stem.2025.12.016]
Abstract:
Ex vivo culture of hematopoietic stem and progenitor cells (HSPCs) is required for gene therapy applications but inadvertently triggers detrimental cellular responses, potentially threatening clinical success. In this study, we employ nichoids, biocompatible 3D culture substrates with cell-scale resolution, to provide HSPCs with mechanical support during ex vivo manipulation. This innovative 3D system improves HSPC multi-lineage differentiation and engraftment capacity by leveraging mechanobiological control over nuclear morphology, cytoskeleton organization, metabolism, and DNA integrity. Notably, 3D culture enables efficient genetic engineering across multiple platforms, including long-range gene editing, base- and prime-editing, and lentiviral-mediated gene addition. Moreover, this scaffold increases the clonal output and persistence of genetically engineered cells in xenotransplantation experiments, including a clinical protocol for lentiviral gene addition in Wiskott-Aldrich syndrome. Overall, we propose a transformative approach to enhance the efficacy and safety of emerging and established hematopoietic stem cell-based gene therapy applications.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
3D culture; clonal tracking; genome editing; hematopoietic stem cells; lentiviral gene transfer; mechanobiology; Wiskott-Aldrich syndrome
Elenco autori:
Midena, F.; Alessandrini, L.; Conci, C.; Barcella, M.; Gazzo, F.; Jacchetti, E.; Carsana, E.; Benedicenti, F.; Vacca, R.; Della Volpe, L.; Arevalo, S.; Giannetti, K.; Barozzi, D.; Franchino, M.; Zonari, E.; Ferrua, F.; Farina, G.; Brombin, C.; Cugnata, F.; Fiumara, M.; Tavella, T.; Cherubin, L.; Fraschetta, F.; Cerullo, G.; Osellame, R.; Radrizzani, M.; Ferrari, S.; Merelli, I.; Gentner, B.; Scielzo, C.; Brendolan, A.; Naldini, L.; Aiuti, A.; Montini, E.; Raimondi, M. T.; Di Micco, R.
Autori di Ateneo:
AIUTI ALESSANDRO
BROMBIN CHIARA
CUGNATA FEDERICA
FERRARI SAMUELE
NALDINI LUIGI
Link alla scheda completa:
https://iris.unisr.it/handle/20.500.11768/201345
Pubblicato in:
CELL STEM CELL
Journal
  • Utilizzo dei cookie

Realizzato con VIVO | Designed by Cineca | 26.5.1.0