| Literature DB >> 29034320 |
Disha Sood1, Karolina Chwalek1, Emily Stuntz1, Dimitra Pouli1, Chuang Du1, Min Tang-Schomer1, Irene Georgakoudi1, Lauren D Black1, David L Kaplan1.
Abstract
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. Since 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.Entities:
Keywords: 3D cell culture; brain; decellularized; extracellular matrix; fetal; matricellular; neurons
Year: 2015 PMID: 29034320 PMCID: PMC5636008 DOI: 10.1021/acsbiomaterials.5b00446
Source DB: PubMed Journal: ACS Biomater Sci Eng ISSN: 2373-9878