Abedin Md Joynal, Michelhaugh Sharon K, Mittal Sandeep, Berdichevsky Yevgeny
Department of Bioengineering, Lehigh University, Bethlehem, PA, United States.
Fralin Biomedical Research Institute, Virginia Tech, Roanoke, VA, United States.
Front Bioeng Biotechnol. 2023 Mar 9;11:1150772. doi: 10.3389/fbioe.2023.1150772. eCollection 2023.
Glioblastoma (GBM) invasiveness and ability to infiltrate deep into the brain tissue is a major reason for the poor patient prognosis for this type of brain cancer. Behavior of glioblastoma cells, including their motility, and expression of invasion-promoting genes such as matrix metalloprotease-2 (MMP2), are strongly influenced by normal cells found in the brain parenchyma. Cells such as neurons may also be influenced by the tumor, as many glioblastoma patients develop epilepsy. models of glioblastoma invasiveness are used to supplement animal models in a search for better treatments, and need to combine capability for high-throughput experiments with capturing bidirectional interactions between GBM and brain cells. In this work, two 3D models of GBM-cortical interactions were investigated. A matrix-free model was created by co-culturing GBM and cortical spheroids, and a matrix-based model was created by embedding cortical cells and a GBM spheroid in Matrigel. Rapid GBM invasion occurred in the matrix-based model, and was enhanced by the presence of cortical cells. Little invasion occurred in the matrix-free model. In both types of models, presence of GBM cells resulted in a significant increase in paroxysmal neuronal activity. Matrix-based model may be better suited for studying GBM invasion in an environment that includes cortical cells, while matrix-free model may be useful in investigation of tumor-associated epilepsy.
胶质母细胞瘤(GBM)的侵袭性以及深入脑组织的能力是这类脑癌患者预后不良的主要原因。胶质母细胞瘤细胞的行为,包括其运动性,以及诸如基质金属蛋白酶-2(MMP2)等促侵袭基因的表达,受到脑实质中正常细胞的强烈影响。诸如神经元等细胞也可能受到肿瘤的影响,因为许多胶质母细胞瘤患者会发生癫痫。胶质母细胞瘤侵袭模型用于补充动物模型以寻找更好的治疗方法,并且需要将高通量实验能力与捕捉GBM和脑细胞之间的双向相互作用相结合。在这项工作中,研究了两种GBM与皮质相互作用的三维模型。通过共培养GBM和皮质球体创建了无基质模型,通过将皮质细胞和GBM球体嵌入基质胶中创建了基于基质的模型。在基于基质的模型中发生了快速的GBM侵袭,并且皮质细胞的存在增强了这种侵袭。在无基质模型中几乎没有侵袭发生。在这两种模型中,GBM细胞的存在导致阵发性神经元活动显著增加。基于基质的模型可能更适合在包含皮质细胞的环境中研究GBM侵袭,而无基质模型可能有助于研究肿瘤相关性癫痫。