During embryogenesis, optic vesicles develop from the diencephalon via a multistep process of organogenesis. Using induced pluripotent stem cell (iPSC)-derived human brain organoids, we attempted to simplify the complexities and demonstrate formation of forebrain-associated bilateral optic vesicles, cellular diversity, and functionality. Around day 30, brain organoids attempt to assemble optic vesicles, which develop progressively as visible structures within 60 days. These optic vesicle-containing brain organoids (OVB-organoids) constitute a developing optic vesicle’s cellular components, including primitive corneal epithelial and lens-like cells, retinal pigment epithelia, retinal progenitor cells, axon-like projections, and electrically active neuronal networks. OVB-organoids also display synapsin-1, CTIP-positive myelinated cortical neurons, and microglia. Interestingly, various light intensities could trigger photosensitive activity of OVB-organoids, and light sensitivities could be reset after transient photobleaching. Thus, brain organoids have the intrinsic ability to self-organize forebrain-associated primitive sensory structures in a topographically restricted manner and can allow interorgan interaction studies within a single organoid.
— Read on www.sciencedirect.com/science/article/pii/S1934590921002952
A new study led by University of Minnesota Twin Cities researchers shows that the stiffness of protein fibers in tissues like collagen, is a key component in controlling the movement of cells. The U.S. National Science Foundation-funded discovery could have a major impact on fields that study cell movement, from regenerative medicine to cancer research.
The research is published in Proceedings of the National Academy of Sciences .
— Read on www.nsf.gov/discoveries/disc_summ.jsp