3D organoids containing endothelial and neural cells generation by serial inductions of differentiation on human iPSC-derived embryoid bodies
Wang, T.; Bagnell, A.; McDonald, V.; Gastfriend, B. D.; Steiner, J. P.; Elkahloun, A. G.; Johnson, K.; Langston, R. G.; Cookson, M. R.; Nath, A.
Show abstract
3D brain organoids have been widely used as a tool to study human brain development and disorders. Although endothelial cells play important roles in the brain development and pathogenesis in neurological disorders, most 3D brain organoids lack inherent endothelial cells and need either the addition of endothelial cells or to be transplanted to animals to reconstitute such vascular structures, likely missing the developmental interactions of endothelial cells and other cells in the human brain. In order to reconstitute a 3D organoid mimicking the in vivo neural and endothelial cells development, we cultured iPSC-derived embryoid bodies in sequentially applied endothelial and neuronal induction media along with Matrigel embedding. The resulting 3D organoid consists of both neural cells and endothelial cells with vascular like structures, as determined by immunostaining. With scRNA-Seq analysis, the brain organoid was confirmed to contain neural cell types similar with human brains, including a variety of excitatory and inhibitory neurons and glia. Furthermore, when compared with traditional cerebral organoids without endothelial cells using RNA-Seq analysis, the endothelial containing neural organoids (EC-neural organoids) showed difference in gene profiles and favored angiogenesis and vasculogenesis. Of the differentially expressed genes, KRBA2 expression was found higher in neural cells and its inhibition by siRNA treatment resulted in decreased transcriptions of a variety of genes such as neuronal differentiation specific genes but not in genes specific to pluripotent stem cells such as OCT4. The EC-neural organoids also express receptors to SARS-CoV-2 similar to human brains. This 3D model provides a useful tool to study the interactions of endothelial cells and neural cells in the brain development and neural infectious disorders where endothelial cells and pericytes play pivotal roles.
Matching journals
The top 9 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- Saxitoxin potentiates Zika virus-induced cell death in human neurons but not in neural progenitors and astrocytes 94%
- Dual SMAD inhibition and Wnt inhibition enhances the differentiation of induced pluripotent stem cells into Retinal Ganglion cells (iPSC-RGCs) 94%
- Retroviral Infection of Human Neurospheres and Use of Stem Cell EVs to Repair Cellular Damage 94%
Similar papers in this journal
- An optimized workflow to generate and characterize iPSC-derived motor neuron (MN) spheroids 95%
- Impaired p53-mediated DNA damage response contributes to microcephaly in Nijmegen Breakage Syndrome patient-derived cerebral organoids 95%
- Transcription factor-mediated generation of dopaminergic neurons from human iPSCs: a comparison of methods 95%
Similar papers in this journal
- AMPK-p38 axis converts human pluripotent stem cells to naïve state 94%
- Differentiation of Mesenchymal Stem/ Stromal Cells into CD45+ Macrophage-like Cells: Expanding Insights into MSC Plasticity 93%
- Induced pluripotent stem cells and cerebral organoids from the critically endangered Sumatran rhinoceros 93%
Similar papers in this journal
- Functional differentiation of Human Dental Pulp Stem Cells into neuron-like cells exhibiting electrophysiological activity 96%
- Emodin-Enhanced hUC-MSC Extracellular Vesicles Alleviate Acute Pancreatitis by Targeting Inflammation and Pyroptosis 94%
- GMP-grade neural progenitor derivation and differentiation from clinical-grade human embryonic stem cells 94%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.