Ultrasound-Activated Piezoelectric Nanoparticles Trigger Microglia Activity Against Glioblastoma Cells.
Maria Cristina CeccarelliCarlotta PucciDaniele De PasqualeAttilio MarinoMaria Cristina CeccarelliMartina MazzuferiMartina BartolucciAndrea PetrettoMirko PratoDoriana DebellisGiorgio De SimoniGiammarino PuglieseMassimiliano LabardiGianni CiofaniPublished in: Advanced healthcare materials (2024)
Glioblastoma 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.
Keyphrases
- drug resistant
- induced apoptosis
- cell cycle arrest
- inflammatory response
- multidrug resistant
- signaling pathway
- white matter
- magnetic resonance imaging
- anti inflammatory
- drug delivery
- spinal cord injury
- acinetobacter baumannii
- squamous cell carcinoma
- cancer therapy
- minimally invasive
- papillary thyroid
- pi k akt
- computed tomography
- pseudomonas aeruginosa
- cerebral ischemia
- squamous cell