Lenti Elisa, Visentin Edoardo, Bojnik Engin, Neroni Alessia, Franchino Martina, Talarico Daniela, Sacchetti Nicolò, Scarfò Lydia, Maurizio Aurora, Garcia-Manteiga Jose Manuel, Ghia Paolo, Brendolan Andrea
Lymphoid Stromal Cell Biology Unit Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute Milan Italy.
B-Cell Neoplasia Unit Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute Milan Italy.
Hemasphere. 2025 Jul 7;9(7):e70170. doi: 10.1002/hem3.70170. eCollection 2025 Jul.
Chronic lymphocytic leukemia (CLL) B cells are characterized by a propensity to undergo rapid apoptosis when cultured in vitro, underscoring the importance of the tissue microenvironment for disease survival. One of the major limitations in studying the role of the microenvironment in tumor development and drug response is the inadequacy of conventional two-dimensional (2D) in vitro assays to physiologically reconstruct the complex spatial organization and interactions of cells in their natural lymphoid niches. To overcome this limitation, we developed a novel in vitro 3D lymph node-like spheroid model of the leukemic microenvironment by culturing human CLL cells with fibroblastic reticular cells (FRCs). FRCs are a key structural component of secondary lymphoid organs and are emerging as crucial players in tissue homeostasis and immune responses. Our results demonstrate that CLL spheroids maintain the physiological cellular ratio between FRCs and leukemic cells over time and protect tumor cells from apoptosis by mimicking the protective effects of the microenvironment. This was further demonstrated by venetoclax treatment that showed reduced apoptosis in 3D compared to a 2D setting. Importantly, the spheroids promote a gene expression profile more aligned with that of CLL cells in lymphoid tissues. The spheroid model provides a straightforward, quick-to-use platform for investigating drug efficacy under conditions that better replicate the natural lymph node microenvironment. This 3D lymph node-like spheroid model could serve as a valuable tool for studying tumor biology and the protective effects of the stromal microenvironment, and for testing therapeutic strategies in a more clinically relevant setting.
慢性淋巴细胞白血病(CLL)B细胞的特点是在体外培养时易于快速凋亡,这突出了组织微环境对疾病存活的重要性。研究微环境在肿瘤发生和药物反应中作用的主要局限之一是传统的二维(2D)体外检测方法不足以在生理层面重建细胞在其自然淋巴微环境中的复杂空间组织和相互作用。为克服这一局限,我们通过将人CLL细胞与成纤维网状细胞(FRCs)共培养,开发了一种新型的白血病微环境体外三维(3D)淋巴结样球体模型。FRCs是次级淋巴器官的关键结构成分,正成为组织稳态和免疫反应中的关键参与者。我们的结果表明,CLL球体随时间推移维持了FRCs与白血病细胞之间的生理细胞比例,并通过模拟微环境的保护作用保护肿瘤细胞免于凋亡。维奈克拉治疗进一步证明了这一点,与二维环境相比,三维环境中细胞凋亡减少。重要的是,球体促进了一种与淋巴组织中CLL细胞更一致的基因表达谱。该球体模型为在能更好模拟天然淋巴结微环境的条件下研究药物疗效提供了一个简单易用的平台。这种三维淋巴结样球体模型可作为研究肿瘤生物学和基质微环境保护作用以及在更具临床相关性的环境中测试治疗策略的宝贵工具。