scholarly journals Using the Gibbs Function as a Measure of Human Brain Development Trends from Fetal Stage to Advanced Age

2020 ◽  
Vol 21 (3) ◽  
pp. 1116
Author(s):  
Edward A. Rietman ◽  
Sophie Taylor ◽  
Hava T. Siegelmann ◽  
Marco A. Deriu ◽  
Marco Cavaglia ◽  
...  

We propose to use a Gibbs free energy function as a measure of the human brain development. We adopt this approach to the development of the human brain over the human lifespan: from a prenatal stage to advanced age. We used proteomic expression data with the Gibbs free energy to quantify human brain’s protein–protein interaction networks. The data, obtained from BioGRID, comprised tissue samples from the 16 main brain areas, at different ages, of 57 post-mortem human brains. We found a consistent functional dependence of the Gibbs free energies on age for most of the areas and both sexes. A significant upward trend in the Gibbs function was found during the fetal stages, which is followed by a sharp drop at birth with a subsequent period of relative stability and a final upward trend toward advanced age. We interpret these data in terms of structure formation followed by its stabilization and eventual deterioration. Furthermore, gender data analysis has uncovered the existence of functional differences, showing male Gibbs function values lower than female at prenatal and neonatal ages, which become higher at ages 8 to 40 and finally converging at late adulthood with the corresponding female Gibbs functions.


Author(s):  
Wai‐Kit Chan ◽  
Rana Fetit ◽  
Rosie Griffiths ◽  
Helen Marshall ◽  
John O Mason ◽  
...  


Author(s):  
Ugomma C. Eze ◽  
Aparna Bhaduri ◽  
Maximilian Haeussler ◽  
Tomasz J. Nowakowski ◽  
Arnold R. Kriegstein

AbstractThe human cortex comprises diverse cell types that emerge from an initially uniform neuroepithelium that gives rise to radial glia, the neural stem cells of the cortex. To characterize the earliest stages of human brain development, we performed single-cell RNA-sequencing across regions of the developing human brain, including the telencephalon, diencephalon, midbrain, hindbrain and cerebellum. We identify nine progenitor populations physically proximal to the telencephalon, suggesting more heterogeneity than previously described, including a highly prevalent mesenchymal-like population that disappears once neurogenesis begins. Comparison of human and mouse progenitor populations at corresponding stages identifies two progenitor clusters that are enriched in the early stages of human cortical development. We also find that organoid systems display low fidelity to neuroepithelial and early radial glia cell types, but improve as neurogenesis progresses. Overall, we provide a comprehensive molecular and spatial atlas of early stages of human brain and cortical development.





2016 ◽  
Vol 16 (1) ◽  
Author(s):  
Jimena Monzón-Sandoval ◽  
Atahualpa Castillo-Morales ◽  
Araxi O. Urrutia ◽  
Humberto Gutierrez


2019 ◽  
Vol 138 ◽  
pp. 33-42 ◽  
Author(s):  
Yusuke Seto ◽  
Mototsugu Eiraku


2018 ◽  
Vol 29 (2) ◽  
pp. 827-837 ◽  
Author(s):  
Riccardo Cafiero ◽  
Jens Brauer ◽  
Alfred Anwander ◽  
Angela D Friederici


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