Engineered extracellular matrices facilitate brain organoids from human pluripotent stem cells

被引:6
|
作者
Muniz, Ayse J. [1 ,2 ]
Topal, Tugba [1 ]
Brooks, Michael D. [3 ]
Sze, Angela [1 ]
Kim, Do Hoon [1 ,4 ]
Jordahl, Jacob [1 ,4 ]
Nguyen, Joe [1 ]
Krebsbach, Paul H. [1 ]
Savelieff, Masha G. [5 ,6 ]
Feldman, Eva L. [5 ,6 ,7 ]
Lahann, Joerg [1 ,2 ,4 ,8 ]
机构
[1] Univ Michigan, Biointerfaces Inst, Ann Arbor, MI USA
[2] Univ Michigan, Macromol Sci & Engn Program, Ann Arbor, MI USA
[3] Univ Michigan, Dept Internal Med, Ann Arbor, MI USA
[4] Univ Michigan, Dept Chem Engn, Ann Arbor, MI USA
[5] Univ Michigan, NeuroNetwork Emerging Therapies, Ann Arbor, MI USA
[6] Univ Michigan, Dept Neurol, Ann Arbor, MI USA
[7] Univ Michigan, NeuroNetwork Emerging Therapies, 5017 AAT BSRB, 109 Zina Pitcher Pl, Ann Arbor, MI 48109 USA
[8] Univ Michigan, Biointerfaces Inst, NCRC Bldg 10, Room A175, 2800 Plymouth Rd, Ann Arbor, MI 48109 USA
来源
基金
美国国家科学基金会;
关键词
PROTEOMIC ANALYSIS; MATRIGEL; DIFFERENTIATION; MORPHOGENESIS; HYDROGELS; DISEASES; NEURONS; BURDEN; MODELS; GROWTH;
D O I
10.1002/acn3.51820
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
ObjectiveBrain organoids are miniaturized in vitro brain models generated from pluripotent stem cells, which resemble full-sized brain more closely than conventional two-dimensional cell cultures. Although brain organoids mimic the human brain's cell-to-cell network interactions, they generally fail to faithfully recapitulate cell-to-matrix interactions. Here, an engineered framework, called an engineered extracellular matrix (EECM), was developed to provide support and cell-to-matrix interactions to developing brain organoids. MethodsWe generated brain organoids using EECMs comprised of human fibrillar fibronectin supported by a highly porous polymer scaffold. The resultant brain organoids were characterized by immunofluorescence microscopy, transcriptomics, and proteomics of the cerebrospinal fluid (CSF) compartment. ResultsThe interstitial matrix-mimicking EECM enhanced neurogenesis, glial maturation, and neuronal diversity from human embryonic stem cells versus conventional protein matrix (Matrigel). Additionally, EECMs supported long-term culture, which promoted large-volume organoids containing over 250 mu L of CSF. Proteomics analysis of the CSF found it superseded previous brain organoids in protein diversity, as indicated by 280 proteins spanning 500 gene ontology pathways shared with adult CSF. InterpretationEngineered EECM matrices represent a major advancement in neural engineering as they have the potential to significantly enhance the structural, cellular, and functional diversity that can be achieved in advanced brain models.
引用
收藏
页码:1239 / 1253
页数:15
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