Jones Hannah E, Robertson Gabriella L, Bodnya Caroline, Romero-Morales Alejandra, O'Rourke Rebecca, Gama Vivian, Siegenthaler Julie A
Department of Pediatrics, Section of Developmental Biology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Cell Biology, Stem Cells and Development Graduate Program, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Stem Cells Dev. 2025 Apr;34(7-8):152-163. doi: 10.1089/scd.2024.0231. Epub 2025 Mar 24.
Neural organoids derived from human-induced pluripotent stem cells (iPSCs) provide a model to study the earliest stages of human brain development, including neurogenesis, neural differentiation, and synaptogenesis. However, neural organoids lack supportive tissues and some non-neural cell types that are key regulators of brain development. Neural organoids have instead been cocultured with non-neural structures and cell types to promote their maturation and model interactions with neuronal cells. One component of the brain that does not form de novo in neural organoids is the meninges, a trilayered structure that surrounds the central nervous system and secretes key signaling molecules required for mammalian brain development. Most studies of meninges-brain signaling have been performed in mice or using two-dimensional cultures of human cells, which do not accurately recapitulate the architecture and cellular diversity of the tissue. To overcome this, we developed a coculture system of neural organoids generated from human iPSCs fused with fetal leptomeninges (LPM) from mice with fluorescently labeled meninges (Col1a1-GFP), which we call leptomeningeal neural organoid (LMNO) fusions. This proof-of-concept study tests the stability of the different cell types in the LPM (fibroblasts and macrophages) and the fused neural organoid (progenitors and neurons), as well as the interface between the organoid and meningeal tissue. We test the longevity of the fusion pieces after 30 and 60 days in culture, describe best practices for preparing the meninges sample before fusion, and examine the feasibility of single or multiple meninges pieces fused to a single organoid. We discuss potential uses of the current version of the LMNO fusion model and opportunities to improve the system.
源自人诱导多能干细胞(iPSC)的神经类器官为研究人类大脑发育的最早阶段提供了一个模型,包括神经发生、神经分化和突触形成。然而,神经类器官缺乏支持组织以及一些作为大脑发育关键调节因子的非神经细胞类型。相反,神经类器官已与非神经结构和细胞类型共培养,以促进其成熟并模拟与神经元细胞的相互作用。神经类器官中无法从头形成的大脑组成部分之一是脑膜,它是围绕中枢神经系统的三层结构,分泌哺乳动物大脑发育所需的关键信号分子。大多数关于脑膜 - 脑信号传导的研究是在小鼠中进行的,或者使用人类细胞的二维培养,这并不能准确地再现该组织的结构和细胞多样性。为了克服这一问题,我们开发了一种共培养系统,将源自人iPSC的神经类器官与来自带有荧光标记脑膜(Col1a1 - GFP)的小鼠的胎儿软脑膜(LPM)融合,我们将其称为软脑膜神经类器官(LMNO)融合体。这项概念验证研究测试了LPM中不同细胞类型(成纤维细胞和巨噬细胞)以及融合的神经类器官(祖细胞和神经元)的稳定性,以及类器官与脑膜组织之间的界面。我们测试了培养30天和60天后融合块的寿命,描述了融合前制备脑膜样本的最佳方法,并研究了将单个或多个脑膜块融合到单个类器官的可行性。我们讨论了当前版本的LMNO融合模型的潜在用途以及改进该系统的机会。