神经科学
生物
脑膜瘤
个体发育
神经组阅片室
多样性(政治)
电池类型
神经外科
祖细胞
病理
神经学
起源细胞
解剖
细胞
医学
进化生物学
中枢神经系统
再生(生物学)
介入放射学
作者
M. Necmettin Pamir,Ayça Erşen-Danyeli,Koray Özduman
标识
DOI:10.1007/s00701-026-06908-1
摘要
BACKGROUND: For over a century, the dominant hypothesis has maintained that meningiomas arise exclusively from arachnoid cap cells. However, emerging evidence from single-cell transcriptomics, spatial sequencing, developmental biology, and transgenic animal models suggests a significantly more complex and heterogeneous cellular origin. METHODS: This mini-review revisits historical perspectives and critically evaluates the limitations of the traditional arachnoid-based paradigm. By synthesizing classical histological insights with contemporary molecular and proteomic data, the study explores alternative hypotheses, particularly those implicating fibroblast-like or regionally distinct meningeal progenitors. RESULTS: The synthesis of multi-omic and developmental data indicates that a singular cellular source is insufficient to account for the clinical and biological diversity of meningiomas. Findings suggest that meningioma ontogeny is likely driven by a broader spectrum of progenitors whose characteristics vary according to anatomical location and embryological lineage. CONCLUSIONS: A redefinition of meningioma ontogeny is necessary. Future classification and therapeutic strategies should reflect the inherent diversity of their cellular sources and anatomical environments, moving beyond the classical arachnoid-cap-cell model.
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