Ultrasound‐Activated Piezoelectric Nanoparticles Trigger Microglia Activity Against Glioblastoma Cells

Author:

Montorsi Margherita12ORCID,Pucci Carlotta1,De Pasquale Daniele1,Marino Attilio1,Ceccarelli Maria Cristina12,Mazzuferi Martina3,Bartolucci Martina4,Petretto Andrea4,Prato Mirko5,Debellis Doriana6,De Simoni Giorgio7,Pugliese Giammarino8,Labardi Massimiliano9,Ciofani Gianni1ORCID

Affiliation:

1. Istituto Italiano di Tecnologia Smart Bio‐Interfaces Viale Rinaldo Piaggio 34 Pontedera 56025 Italy

2. Scuola Superiore Sant'Anna The BioRobotics Institute Viale Rinaldo Piaggio 34 Pontedera 56025 Italy

3. Politecnico di Torino DIMEAS Corso Duca degli Abruzzi 24 Torino 10129 Italy

4. IRCCS Istituto Giannina Gaslini Core Facilities‐Clinical Proteomics and Metabolomics Via Gerolamo Gaslini 5 Genova 16147 Italy

5. Istituto Italiano di Tecnologia Materials Characterization Facility Via Morego 30 Genova 16163 Italy

6. Istituto Italiano di Tecnologia Electron Microscopy Facility Via Morego 30 Genova 16163 Italy

7. CNR Nanoscience Institute NEST Laboratory Piazza San Silvestro 12 Pisa 56127 Italy

8. Istituto Italiano di Tecnologia Chemistry Facility Via Morego 30 Genova 16163 Italy

9. CNR‐IPCF Sede Secondaria di Pisa Largo Pontecorvo 3 Pisa 56127 Italy

Abstract

AbstractGlioblastoma multiforme (GBM) is the most aggressive brain cancer, characterized by a rapid and drug‐resistant progression. GBM “builds” around its primary core a genetically heterogeneous tumor‐microenvironment (TME), recruiting surrounding healthy brain cells by releasing various intercellular signals. Glioma‐associated microglia (GAM) represent the largest population of collaborating cells, which, in the TME, usually exhibit the anti‐inflammatory M2 phenotype, thus promoting an immunosuppressing environment that helps tumor growth. Conversely, “classically activated” M1 microglia could provide proinflammatory and antitumorigenic activity, expected to exert a beneficial effect in defeating glioblastoma. In this work, an immunotherapy approach based on proinflammatory modulation of the GAM phenotype is proposed, through a controlled and localized electrical stimulation. The developed strategy relies on the wireless ultrasonic excitation of polymeric piezoelectric nanoparticles coated with GBM cell membrane extracts, to exploit homotypic targeting in antiglioma applications. Such camouflaged nanotransducers locally generate electrical cues on GAM membranes, activating their M1 phenotype and ultimately triggering a promising anticancer activity. Collected findings open new perspectives in the modulation of immune cell activities through “smart” nanomaterials and, more specifically, provide an innovative auspicious tool in glioma immunotherapy.

Publisher

Wiley

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