Bidirectional cell-matrix interaction dictates neuronal network formation in a brain-mimetic 3D scaffold

被引:16
作者
Samanta, Sumanta [1 ]
Ylae-Outinen, Laura [2 ,3 ]
Rangasami, Vignesh Kumar [1 ]
Narkilahti, Susanna [2 ]
Oommen, Oommen P. [1 ]
机构
[1] Tampere Univ, Fac Med & Hlth Technol, Bioengn & Nanomed Grp, Tampere 33720, Finland
[2] Tampere Univ, Fac Med & Hlth Technol, NeuroGrp, Tampere, Finland
[3] Univ Jyvaskyla, Fac Sports & Hlth Sci, Jyvaskyla, Finland
基金
芬兰科学院; 欧盟地平线“2020”;
关键词
Neuronal network; Human pluripotent stem cells; Hyaluronic acid; Chondroitin sulfate; Dopamine; Brain-mimetic hydrogel scaffold; IN-VITRO; HYDROGELS; DIFFERENTIATION; OUTGROWTH; STROKE;
D O I
10.1016/j.actbio.2021.12.010
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Human pluripotent stem cells (hPSC) derived neurons are emerging as a powerful tool for studying neurobiology, disease pathology, and modeling. Due to the lack of platforms available for housing and growing hPSC-derived neurons, a pressing need exists to tailor a brain-mimetic 3D scaffold that reca-pitulates tissue composition and favourably regulates neuronal network formation. Despite the progress in engineering biomimetic scaffolds, an ideal brain-mimetic scaffold is still elusive. We bioengineered a physiologically relevant 3D scaffold by integrating brain-like extracellular matrix (ECM) components and chemical cues. Culturing hPSCs-neurons in hyaluronic acid (HA) gels and HA-chondroitin sulfate (HA-CS) composite gels showed that the CS component prevails as the predominant factor for the growth of neuronal cells, albeit to modest efficacy. Covalent grafting of dopamine (DA) moieties to the HA-CS gel (HADA-CS) enhanced the scaffold stability and stimulated the gel's remodeling properties by entrap-ping cell-secreted laminin, and binding brain-derived neurotrophic factor (BDNF). Neurons cultured in the scaffold expressed Col1, Col11, and ITGB4; important for cell adhesion and cell-ECM signaling. Thus, the HA-CS scaffold with integrated chemical cues (DA) supported neuronal growth and network formation. This scaffold offers a valuable tool for tissue engineering and disease modeling and helps in bridging the gap between animal models and human diseases by providing biomimetic neurophysiology.Statement of significance Developing a brain mimetic 3D scaffold that supports neuronal growth could potentially be useful to study neurobiology, disease pathology, and disease modeling. However, culturing human induced pluripo-tent stem cells (hiPSC) and human embryonic stem cells (ESCs) derived neurons in a 3D matrix is ex-tremely challenging as neurons are very sensitive cells and require tailored composition, viscoelasticity, and chemical cues. This article identified the key chemical cues necessary for designing neuronal matrix that trap the cell-produced ECM and neurotrophic factors and remodel the matrix and supports neurite outgrowth. The tailored injectable scaffold possesses self-healing/shear-thinning property which is use-ful to design injectable gels for regenerative medicine and disease modeling that provides biomimetic neurophysiology.(c) 2021 The Author(s). Published by Elsevier Ltd on behalf of Acta Materialia Inc. This is an open access article under the CC BY license ( http://creativecommons.org/licenses/by/4.0/ )
引用
收藏
页码:314 / 323
页数:10
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