Recapitulation of Human Neural Microenvironment Signatures in iPSC-Derived NPC 3D Differentiation

被引:54
作者
Simao, Daniel [1 ,2 ]
Silva, Marta M. [1 ,2 ]
Terrasso, Ana P. [1 ,2 ]
Arez, Francisca [1 ,2 ]
Sousa, Marcos F. Q. [1 ,2 ]
Mehrjardi, Narges Z. [3 ]
Saric, Tomo [3 ]
Gomes-Alves, Patricia [1 ,2 ]
Raimundo, Nuno [4 ]
Alves, Paula M. [1 ,2 ]
Brito, Catarina [1 ,2 ]
机构
[1] Inst Biol Expt & Biol, iBET, Oeiras, Portugal
[2] Univ Nova Lisboa, Inst Tecnol Quim & Biol Antonio Xavier, Oeiras, Portugal
[3] Univ Cologne, Med Fac, Ctr Physiol & Pathophysiol, Inst Neurophysiol, D-50931 Cologne, Germany
[4] Univ Med Gottingen, Inst Zellbiochem, Gottingen, Germany
来源
STEM CELL REPORTS | 2018年 / 11卷 / 02期
基金
欧洲研究理事会;
关键词
PLURIPOTENT STEM-CELLS; CENTRAL-NERVOUS-SYSTEM; EXTRACELLULAR-MATRIX; CEREBRAL ORGANOIDS; BRAIN; ADHESION; NEURONS; METALLOPROTEINASES; PROTEOGLYCANS; SPECIFICATION;
D O I
10.1016/j.stemcr.2018.06.020
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Brain microenvironment plays an important role in neurodevelopment and pathology, where the extracellular matrix (ECM) and soluble factors modulate multiple cellular processes. Neural cell culture typically relies on heterologous matrices poorly resembling brain ECM. Here, we employed neurospheroids to address microenvironment remodeling during neural differentiation of human stem cells, without the confounding effects of exogenous matrices. Proteome and transcriptome dynamics revealed significant changes at cell membrane and ECM during 3D differentiation, diverging significantly from the 2D differentiation. Structural proteoglycans typical of brain ECM were enriched during 3D differentiation, in contrast to basement membrane constituents in 2D. Moreover, higher expression of synaptic and ion transport machinery was observed in 3D cultures, suggesting higher neuronal maturation in neurospheroids. This work demonstrates that 3D neural differentiation as neurospheroids promotes the expression of cellular and extracellular features found in neural tissue, highlighting its value to address molecular defects in cell-ECM interactions associated with neurological disorders.
引用
收藏
页码:552 / 564
页数:13
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