Glial cells provide physical and chemical support and protection for neurons. Secreted neurotrophic factors, scaffolds and vesicles regulate in addition to normal homeostasis, repair following neural tissue injury or degeneration. We previously demonstrated that human CNS glia have revascularization capacity by inducing endothelial cell sprouting and microchanneling driven by glial cell secreted components. The clinical potential of using secreted factors and vesicles generated by glial cells in conditioned media was shown by their re-normalization of pathological blood vessels and 3D tissue wound healing and remodeling capacity. To identify secreted components of glial cells and how CNS and PNS glial cells differentially regulate neural tissue homeostasis, disease and injury response, we developed a novel culture method for various types of glial cells that allow for isolating and characterizing secreted glial components, free of animal factors and contaminants normally associated with serum-based culture conditions. Our culture method will enable to identify secreted components using ultrasensitive RNA, glycoconjugate and protein analysis technologies. The characterization of glial secreted factors involved microchanneling may help in development of new clinical therapies for glial and neural cells or axons to migrate and reform connections.

Three-dimensional cultures for collecting CNS and PNS glial secreted factors, vesicles and scaffolds free of animal serum components / C. Cocola, T. Mohamed, E. Piscitelli, P. Pelucchi, E. Abeni, E. Mosca, G.D. Petro, G. Porta, J. Kehler, M. Götte, I. Zucchi, V. Magnaghi, R. Reinbold. - (2023 Dec 04). [10.20944/preprints202312.0115.v1]

Three-dimensional cultures for collecting CNS and PNS glial secreted factors, vesicles and scaffolds free of animal serum components

T. Mohamed;V. Magnaghi
Penultimo
;
2023

Abstract

Glial cells provide physical and chemical support and protection for neurons. Secreted neurotrophic factors, scaffolds and vesicles regulate in addition to normal homeostasis, repair following neural tissue injury or degeneration. We previously demonstrated that human CNS glia have revascularization capacity by inducing endothelial cell sprouting and microchanneling driven by glial cell secreted components. The clinical potential of using secreted factors and vesicles generated by glial cells in conditioned media was shown by their re-normalization of pathological blood vessels and 3D tissue wound healing and remodeling capacity. To identify secreted components of glial cells and how CNS and PNS glial cells differentially regulate neural tissue homeostasis, disease and injury response, we developed a novel culture method for various types of glial cells that allow for isolating and characterizing secreted glial components, free of animal factors and contaminants normally associated with serum-based culture conditions. Our culture method will enable to identify secreted components using ultrasensitive RNA, glycoconjugate and protein analysis technologies. The characterization of glial secreted factors involved microchanneling may help in development of new clinical therapies for glial and neural cells or axons to migrate and reform connections.
glial cells; neurogenesis; vasculogenic mimicry; microchanneling; central nervous system; peripheral nervous system; 2D and 3D serum replacement culture; glycoconjugates; vesicles
Settore BIO/09 - Fisiologia
   Molecular pathways in Schwannomatosis: exploiting in vitro models for the identification of new therapeutic targets
   MINISTERO DELL'ISTRUZIONE E DEL MERITO
   2017BJJ5EE_001
4-dic-2023
https://www.preprints.org/manuscript/202312.0115/v1
File in questo prodotto:
File Dimensione Formato  
preprints202312.0115.v1.pdf

accesso aperto

Tipologia: Pre-print (manoscritto inviato all'editore)
Dimensione 852.83 kB
Formato Adobe PDF
852.83 kB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1026890
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact