Smith Ian M, Hengen Autumn C, Abraham Ariel W, Majeti Venkata Sai Pranav, Banerjee Shohini, Givpoor Nikka, Moses Allison K, Stroka Kimberly M
Fischell Department of Bioengineering, University of Maryland, College Park, MD 20742, USA.
Department of Bioengineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Am J Physiol Cell Physiol. 2025 Aug 20. doi: 10.1152/ajpcell.00408.2025.
Aquaporins are water transport proteins that regulate pro-metastatic behaviors in cancer, including cell invasion, proliferation, and epithelial-to-mesenchymal transition. Aquaporin 5, an isoform virtually absent from healthy tissues, is overexpressed in numerous cancer types. Studies have connected Aquaporin 5 to the migratory and invasive properties of single cells in two-dimensional assays; however, the role of Aquaporin 5 in inducing invasive phenotypes in models that recapitulate the tumor microenvironment remains unknown. To address this gap, MDA-MB-231 cell lines were created with Aquaporin 5 overexpression and knockdown to identify the resulting single and collective cell motility in three-dimensional models. Upon validating the developed cell lines, Aquaporin 5 expression regulated cell motility and invasion in varied biaxial microenvironments. Additionally, Aquaporin 5 was found to play a unique role in regulating MDA-MB-231 spheroid development, influencing the formation, size, circularity, and adhesion, distinct from its function in two-dimensional models. Finally, increased Aquaporin 5 expression intensified the invasive capacity of spheroid multicellular protrusions by polarizing to their invasive front. In summary, this work expands upon the knowledge that Aquaporin 5 enhances cell motility, while elucidating the previously unreported adhesive and multicellular invasive effects of Aquaporin 5 in a three-dimensional model.
水通道蛋白是调节癌症中促转移行为的水转运蛋白,包括细胞侵袭、增殖和上皮-间质转化。水通道蛋白5在健康组织中几乎不存在,却在多种癌症类型中过度表达。研究已将水通道蛋白5与二维实验中单个细胞的迁移和侵袭特性联系起来;然而,水通道蛋白5在模拟肿瘤微环境的模型中诱导侵袭表型的作用仍不清楚。为填补这一空白,构建了水通道蛋白5过表达和敲低的MDA-MB-231细胞系,以确定在三维模型中由此产生的单个细胞和集体细胞运动性。在验证所构建的细胞系后,发现水通道蛋白5的表达在不同的双轴微环境中调节细胞运动性和侵袭。此外,还发现水通道蛋白5在调节MDA-MB-231球体发育中发挥独特作用,影响其形成、大小、圆形度和黏附,这与其在二维模型中的功能不同。最后,水通道蛋白5表达的增加通过使其极化到侵袭前沿增强了球体多细胞突起的侵袭能力。总之,这项工作扩展了对水通道蛋白5增强细胞运动性的认识,同时阐明了水通道蛋白5在三维模型中以前未报道的黏附及多细胞侵袭作用。