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  3. SCSB Lunch Series: Impact of cellular metabolism on corticogenesis – an observation from human cortical organoid culture
SCSB Lunch Series: Impact of cellular metabolism on corticogenesis – an observation from human cortical organoid culture
Simons Center for the Social Brain

SCSB Lunch Series: Impact of cellular metabolism on corticogenesis – an observation from human cortical organoid culture

Add to CalendarAmerica/New_YorkSCSB Lunch Series: Impact of cellular metabolism on corticogenesis – an observation from human cortical organoid culture12/03/2021 12:00 pm12/03/2021 1:00 pm,
December 3, 2021
12:00 pm - 1:00 pm
Location
,
Contact
asokhina@mit.edu
    Description

    Date: Friday, December 3, 2021
    Time: 12:00pm – 1:00pm
    Location: Zoom meeting – Registration Required
    Register in advance for this talk: click here
    * After registering, you will receive a confirmation email containing information on how to join the talk.

    Speaker: Shaoyu Lin, Ph.D.
    Affiliation: Simons Fellow, Kwanghun Chung Laboratory, Picower Institute for Learning and Memory, Institute of Medical Engineering and Science, MIT
    Host: Dr. Kwanghun Chung

    Talk title: Impact of cellular metabolism on corticogenesis – an observation from human cortical organoid culture

    Abstract: 3D-cultured human stem cell-derived cortical organoids can mimic broad features of developing human cortex. However, even with the best protocol developed so far, many fundamental aspects of human corticogenesis have not been fully recapitulated in organoid culture yet. This has been partially due to aberrantly accelerated radial glia differentiation in an overall non-ideal in vitro environment. Here, our preliminary study has shown, after being cultured in hypothermal conditions to slow down metabolism, that the cortical organoids can grow with significantly enlarged size and more importantly, a remarkably increased neuronal production, particularly the upper-layer cortical neurons, which led to improved cortical lamination. Such phenotype can be attributed to an enlarged proliferating progenitor pool and a prolonged neurogenic time window. Our study revealed an unexpected relationship between cellular metabolism and corticogenesis, and strongly suggests that metabolic manipulation holds great promise as a more “universal” strategy to modulate neurodevelopment.

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