小胶质细胞
促炎细胞因子
胶质瘤
免疫系统
免疫疗法
表型
人口
肿瘤微环境
表型筛选
神经科学
生物
医学
癌症研究
炎症
免疫学
基因
生物化学
环境卫生
作者
Margherita Montorsi,Carlotta Pucci,Daniele De Pasquale,Attilio Marino,Maria Cristina Ceccarelli,Martina Mazzuferi,Martina Bartolucci,Andrea Petretto,Mirko Prato,Doriana Debellis,Giorgio De Simoni,Giammarino Pugliese,M. Labardi,Gianni Ciofani
标识
DOI:10.1002/adhm.202304331
摘要
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.
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