Revealing the Impact of Mitochondrial Fitness During Early Neural Development Using Human Brain Organoids

被引:0
作者
Romero-Morales, Alejandra I. [1 ]
Gama, Vivian [1 ,2 ,3 ]
机构
[1] Vanderbilt Univ, Dept Cell & Dev Biol, Nashville, TN USA
[2] Vanderbilt Univ, Vanderbilt Ctr Stem Cell Biol, Nashville, TN USA
[3] Vanderbilt Univ, Vanderbilt Brain Inst, Nashville, TN USA
来源
FRONTIERS IN MOLECULAR NEUROSCIENCE | 2022年 / 15卷
关键词
stem cells; glycolysis; oxidative phosphorylation; mitochondria; neural precursor cells; neural rosettes; brain organoids; PLURIPOTENT STEM-CELLS; RADIAL GLIAL-CELLS; DYNAMIN-RELATED PROTEIN; HUMAN CEREBRAL-CORTEX; INTERKINETIC NUCLEAR MIGRATION; SUBCORTICAL PROJECTION NEURONS; ADULT HUMAN FIBROBLASTS; HUMAN PREFRONTAL CORTEX; SUBTYPE-SPECIFIC GENES; HUMAN IPSC LINE;
D O I
10.3389/fnmol.2022.840265
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mitochondrial homeostasis -including function, morphology, and inter-organelle communication- provides guidance to the intrinsic developmental programs of corticogenesis, while also being responsive to environmental and intercellular signals. Two- and three-dimensional platforms have become useful tools to interrogate the capacity of cells to generate neuronal and glia progeny in a background of metabolic dysregulation, but the mechanistic underpinnings underlying the role of mitochondria during human neurogenesis remain unexplored. Here we provide a concise overview of cortical development and the use of pluripotent stem cell models that have contributed to our understanding of mitochondrial and metabolic regulation of early human brain development. We finally discuss the effects of mitochondrial fitness dysregulation seen under stress conditions such as metabolic dysregulation, absence of developmental apoptosis, and hypoxia; and the avenues of research that can be explored with the use of brain organoids.
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页数:31
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