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Ex vivo expansion in a clinical grade medium, containing growth factors from human platelets, enhances migration capacity of adipose stem cells.
Agostini, Francesco; Vicinanza, Carla; Lombardi, Elisabetta; Da Ros, Francesco; Marangon, Miriam; Massarut, Samuele; Mazzucato, Mario; Durante, Cristina.
Affiliation
  • Agostini F; Stem Cell Unit, CRO Aviano, National Cancer Institute, IRCCS, Aviano, Italy.
  • Vicinanza C; Stem Cell Unit, CRO Aviano, National Cancer Institute, IRCCS, Aviano, Italy.
  • Lombardi E; Stem Cell Unit, CRO Aviano, National Cancer Institute, IRCCS, Aviano, Italy.
  • Da Ros F; Stem Cell Unit, CRO Aviano, National Cancer Institute, IRCCS, Aviano, Italy.
  • Marangon M; Stem Cell Unit, CRO Aviano, National Cancer Institute, IRCCS, Aviano, Italy.
  • Massarut S; Breast Cancer Surgery Unit, CRO Aviano, National Cancer Institute, IRCCS, Aviano, Italy.
  • Mazzucato M; Stem Cell Unit, CRO Aviano, National Cancer Institute, IRCCS, Aviano, Italy.
  • Durante C; Stem Cell Unit, CRO Aviano, National Cancer Institute, IRCCS, Aviano, Italy.
Front Immunol ; 15: 1404228, 2024.
Article de En | MEDLINE | ID: mdl-38812519
ABSTRACT

Introduction:

Adipose tissue mesenchymal stem/stromal cells (ASC) can be used as advanced therapy medicinal product in regenerative and cancer medicine. We previously demonstrated Supernatant Rich in Growth Factors (SRGF) can replace fetal bovine serum (FBS) to expand ASC by a clinical grade compliant protocol. The therapeutic potential of ASC is based also on their homing capacity toward inflammatory/cancer sites oriented cell migration is a fundamental process in this scenario. We investigated the impact of SRGF on ASC migration properties.

Methods:

The motility/migration potential of ASC expanded in 5% SRGF was analyzed, in comparison to 10% FBS, by standard wound healing, bidimensional chemotaxis and transwell assays, and by millifluidic transwell tests. Mechanisms involved in the migration process were investigated by transient protein overexpression.

Results:

In comparison to standard 10% FBS, supplementation of the cell culture medium with 5% SRGF, strongly increased migration properties of ASC along the chemotactic gradient and toward cancer cell derived soluble factors, both in static and millifluidic conditions. We showed that, independently from applied migratory stimulus, SRGF expanded ASC were characterized by far lower expression of α-smooth muscle actin (αSMA), a protein involved in the cell migration machinery. Overexpression of αSMA induced a significant and marked decrease in migration capacity of SRGF expanded ASC.

Discussion:

In conclusion, 5% SRGF addition in the cell culture medium increases the migration potential of ASC, reasonably through appropriate downregulation of αSMA. Thus, SRGF could potentially improve the therapeutic impact of ASC, both as modulators of the immune microenviroment or as targeted drug delivery vehicles in oncology.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Plaquettes / Mouvement cellulaire / Tissu adipeux / Protéines et peptides de signalisation intercellulaire / Cellules souches mésenchymateuses Limites: Female / Humans Langue: En Journal: Front Immunol Année: 2024 Type de document: Article Pays d'affiliation: Italie Pays de publication: Suisse

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Plaquettes / Mouvement cellulaire / Tissu adipeux / Protéines et peptides de signalisation intercellulaire / Cellules souches mésenchymateuses Limites: Female / Humans Langue: En Journal: Front Immunol Année: 2024 Type de document: Article Pays d'affiliation: Italie Pays de publication: Suisse