4.6 Article

Fetal Brain Extracellular Matrix Boosts Neuronal Network Formation in 3D Bioengineered Model of Cortical Brain Tissue

期刊

ACS BIOMATERIALS SCIENCE & ENGINEERING
卷 2, 期 1, 页码 131-140

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsbiomaterials.5b00446

关键词

fetal; brain; extracellular matrix; matricellular; 3D cell culture; neurons; decellularized

资金

  1. US National Institutes of Health (NIH) P41 Tissue Engineering Resource Center [EB002520]
  2. NIH R01 [NS092847]
  3. German Research Foundation (DFG) [CH 1400/2-1]
  4. NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [P41EB002520] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS092847] Funding Source: NIH RePORTER

向作者/读者索取更多资源

The extracellular matrix (ECM) constituting up to 20% of the organ volume is a significant component of the brain due to its instructive role in the compartmentalization of functional microdomains in every brain structure. The composition, quantity, and structure of ECM changes dramatically during the development of an organism greatly contributing to the remarkably sophisticated architecture and function of the brain. Because fetal brain is highly plastic, we hypothesize that the fetal brain ECM may contain cues promoting neural growth and differentiation, highly desired in regenerative medicine. Thus, we studied the effect of brain derived fetal and adult ECM complemented with matricellular proteins on cortical neurons using in vitro 3D bioengineered model of cortical brain tissue. The tested parameters included neuronal network density, cell viability, calcium signaling, and electrophysiology. Both adult and fetal brain ECM as well as matricellular proteins significantly improved neural network formation as compared to single-component, collagen I matrix. Additionally, the brain ECM improved cell viability and lowered glutamate release. The fetal brain ECM induced superior neural network formation, calcium signaling, and spontaneous spiking activity over adult brain ECM. This study highlights the difference in the neuroinductive properties of fetal and adult brain ECM and suggests that delineating the basis for this divergence may have implications for regenerative medicine.

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