Bioengineering tissue morphogenesis and function in human neural organoids

• Published in: Seminars in cell & developmental biology 2021-03, Vol.111, p.52-59
• Main Authors: Fedorchak, Nikolai J., Iyer, Nisha, Ashton, Randolph S.
• Format: Article
• Language: English
• Subjects: Assembloids; Bioengineering - methods; Brain - cytology; Brain - physiology; Cell Differentiation; Circuit formation; Endothelial Cells - cytology; Endothelial Cells - physiology; Extracellular Matrix - metabolism; Humans; Models, Biological; Morphogenesis - physiology; Morphogenetic patterning; Neovascularization, Physiologic; Network maturation; Neural Stem Cells - cytology; Neural Stem Cells - physiology; Neural Stem Cells - transplantation; Neurogenesis - physiology; Neuroglia - cytology; Neuroglia - physiology; Neurons - cytology; Neurons - physiology; Neurons - transplantation; Organoids - cytology; Organoids - physiology; Pluripotent Stem Cells - cytology; Pluripotent Stem Cells - physiology; Signaling centers; Tissue Engineering - methods; Tissue morphology; Vascularization
• ISSN: 1084-9521; 1096-3634
• DOI: 10.1016/j.semcdb.2020.05.025

Over the last decade, scientists have begun to model CNS development, function, and disease in vitro using human pluripotent stem cell (hPSC)-derived organoids. Using traditional protocols, these 3D tissues are generated by combining the innate emergent properties of differentiating hPSC aggregates with a bioreactor environment that induces interstitial transport of oxygen and nutrients and an optional supportive hydrogel extracellular matrix (ECM). During extended culture, the hPSC-derived neural organoids (hNOs) obtain millimeter scale sizes with internal microscale cytoarchitectures, cellular phenotypes, and neuronal circuit behaviors mimetic of those observed in the developing brain, eye, or spinal cord. Early studies evaluated the cytoarchitectural and phenotypical character of these organoids and provided unprecedented insight into the morphogenetic processes that govern CNS development. Comparisons to human fetal tissues revealed their significant similarities and differences. While hNOs have current disease modeling applications and significant future promise, their value as anatomical and physiological models is limited because they fail to form reproducibly and recapitulate more mature in vivo features. These include biomimetic macroscale tissue morphology, positioning of morphogen signaling centers to orchestrate appropriate spatial organization and intra- and inter-connectivity of discrete tissue regions, maturation of physiologically relevant neural circuits, and formation of vascular networks that can support sustained in vitro tissue growth. To address these inadequacies scientists have begun to integrate organoid culture with bioengineering techniques and methodologies including genome editing, biomaterials, and microfabricated and microfluidic platforms that enable spatiotemporal control of cellular differentiation or the biochemical and biophysical cues that orchestrate organoid morphogenesis. This review will examine recent advances in hNO technologies and culture strategies that promote reproducible in vitro morphogenesis and greater biomimicry in structure and function.