| Literature DB >> 32595422 |
Daeha Joung1, Vincent Truong2, Colin C Neitzke2, Shuang-Zhuang Guo1, Patrick J Walsh2, Joseph R Monat1, Fanben Meng1, Sung Hyun Park1, James R Dutton3, Ann M Parr2, Michael C McAlpine1.
Abstract
A bioengineered spinal cord is fabricated via extrusion-based multi-material 3D bioprinting, in which clusters of induced pluripotent stem cell (iPSC)-derived spinal neuronal progenitor cells (sNPCs) and oligodendrocyte progenitor cells (OPCs) are placed in precise positions within 3D printed biocompatible scaffolds during assembly. The location of a cluster of cells, of a single type or multiple types, is controlled using a point-dispensing printing method with a 200 μm center-to-center spacing within 150 μm wide channels. The bioprinted sNPCs differentiate and extend axons throughout microscale scaffold channels, and the activity of these neuronal networks is confirmed by physiological spontaneous calcium flux studies. Successful bioprinting of OPCs in combination with sNPCs demonstrates a multicellular neural tissue engineering approach, where the ability to direct the patterning and combination of transplanted neuronal and glial cells can be beneficial in rebuilding functional axonal connections across areas of central nervous system (CNS) tissue damage. This platform can be used to prepare novel biomimetic, hydrogel-based scaffolds modeling complex CNS tissue architecture in vitro and harnessed to develop new clinical approaches to treat neurological diseases, including spinal cord injury.Entities:
Keywords: 3D bioprinting; induced pluripotent stem cells; neural progenitor cells; spinal cord scaffolds; tissue engineering
Year: 2018 PMID: 32595422 PMCID: PMC7319181 DOI: 10.1002/adfm.201801850
Source DB: PubMed Journal: Adv Funct Mater ISSN: 1616-301X Impact factor: 18.808