| Literature DB >> 34354063 |
Ann-Na Cho1, Yoonhee Jin1, Yeonjoo An1, Jin Kim1, Yi Sun Choi1, Jung Seung Lee1, Junghoon Kim1, Won-Young Choi2, Dong-Jun Koo3, Weonjin Yu4, Gyeong-Eon Chang1, Dong-Yoon Kim3, Sung-Hyun Jo5, Jihun Kim6, Sung-Yon Kim3,7, Yun-Gon Kim5, Ju Young Kim8, Nakwon Choi9, Eunji Cheong1, Young-Joon Kim2, Hyunsoo Shawn Je4, Hoon-Chul Kang6, Seung-Woo Cho10,11,12.
Abstract
Brain organoids derived from human pluripotent stem cells provide a highly valuable in vitro model to recapitulate human brain development and neurological diseases. However, the current systems for brain organoid culture require further improvement for the reliable production of high-quality organoids. Here, we demonstrate two engineering elements to improve human brain organoid culture, (1) a human brain extracellular matrix to provide brain-specific cues and (2) a microfluidic device with periodic flow to improve the survival and reduce the variability of organoids. A three-dimensional culture modified with brain extracellular matrix significantly enhanced neurogenesis in developing brain organoids from human induced pluripotent stem cells. Cortical layer development, volumetric augmentation, and electrophysiological function of human brain organoids were further improved in a reproducible manner by dynamic culture in microfluidic chamber devices. Our engineering concept of reconstituting brain-mimetic microenvironments facilitates the development of a reliable culture platform for brain organoids, enabling effective modeling and drug development for human brain diseases.Entities:
Year: 2021 PMID: 34354063 DOI: 10.1038/s41467-021-24775-5
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919