scholarly journals White Matter Interstitial Neurons in the Adult Human Brain: 3% of Cortical Neurons in Quest for Recognition

Cells ◽  
2021 ◽  
Vol 10 (1) ◽  
pp. 190
Author(s):  
Goran Sedmak ◽  
Miloš Judaš

White matter interstitial neurons (WMIN) are a subset of cortical neurons located in the subcortical white matter. Although they were fist described over 150 years ago, they are still largely unexplored and often considered a small, functionally insignificant neuronal population. WMIN are adult remnants of neurons located in the transient fetal subplate zone (SP). Following development, some of the SP neurons undergo apoptosis, and the remaining neurons are incorporated in the adult white matter as WMIN. In the adult human brain, WMIN are quite a large population of neurons comprising at least 3% of all cortical neurons (between 600 and 1100 million neurons). They include many of the morphological neuronal types that can be found in the overlying cerebral cortex. Furthermore, the phenotypic and molecular diversity of WMIN is similar to that of the overlying cortical neurons, expressing many glutamatergic and GABAergic biomarkers. WMIN are often considered a functionally unimportant subset of neurons. However, upon closer inspection of the scientific literature, it has been shown that WMIN are integrated in the cortical circuitry and that they exhibit diverse electrophysiological properties, send and receive axons from the cortex, and have active synaptic contacts. Based on these data, we are able to enumerate some of the potential WMIN roles, such as the control of the cerebral blood flow, sleep regulation, and the control of information flow through the cerebral cortex. Also, there is a number of studies indicating the involvement of WMIN in the pathophysiology of many brain disorders such as epilepsy, schizophrenia, Alzheimer’s disease, etc. All of these data indicate that WMIN are a large population with an important function in the adult brain. Further investigation of WMIN could provide us with novel data crucial for an improved elucidation of the pathophysiology of many brain disorders. In this review, we provide an overview of the current WMIN literature, with an emphasis on studies conducted on the human brain.

10.1038/nm837 ◽  
2003 ◽  
Vol 9 (4) ◽  
pp. 439-447 ◽  
Author(s):  
Marta C. Nunes ◽  
Neeta Singh Roy ◽  
H. Michael Keyoung ◽  
Robert R. Goodman ◽  
Guy McKhann ◽  
...  

2010 ◽  
Vol 41 (01) ◽  
Author(s):  
M Taubert ◽  
B Draganski ◽  
A Anwander ◽  
K Müller ◽  
A Horstmann ◽  
...  

2001 ◽  
Vol 46 (2) ◽  
pp. 401-406 ◽  
Author(s):  
Jinyuan Zhou ◽  
Xavier Golay ◽  
Peter C.M. van Zijl ◽  
M. Johanna Silvennoinen ◽  
Risto Kauppinen ◽  
...  

Biologia ◽  
2009 ◽  
Vol 64 (4) ◽  
Author(s):  
Ivana Macikova ◽  
Anna Perzelova ◽  
Peter Mraz ◽  
Ivan Bizik ◽  
Juraj Steno

AbstractTraditionally, astrocytes are divided into fibrous and protoplasmic types based on their morphologic appearance. Here the cultures were prepared separately from the adult human cortical gray and white matter of brain biopsies. Both cultures differed only in the number of glial fibrillary acidic protein (GFAP)-positive cells. In the gray matter these were absent or rare, whereas in confluent cultures from the white matter they reached 0.1% of all cells. Three main morphologic types of GFAP-positive cells were found in this study: stellate, bipolar and large flat cells. GFAP-positive cells with two or three long processes mimic a neuron-like morphology. We did not find process-bearing cells expressing neuronal markers (MAP-2, NF, and N-CAM). The conflicting reports concerning GFAP immunostaining and the study dealing with the presence of putative neurons in adult human brain cultures are discussed with respect to these findings. The latter classification of astrocytes into type 1 and type 2 is based on immunostaining to A2B5 antigen: type 1 (GFAP+/A2B5−) and type 2 (GFAP+/A2B5+) astrocytes are proposed to be analogous to protoplasmic and fibrous astrocytes, respectively. In adult human brain cultures we found only small amount of A2B5-positive cells. Double immunofluorescence revealed that astroglial cells of similar fibrous or bipolar shape grown on one coverslip were either GFAP+/A2B5+ or GFAP+/A2B5−. On the other hand, the A2B5+/GFAP− immunophenotype was not observed. These results indicate that in general the cell phenotype from adult human brain tissue is not well established when they are in culture.


Cell Reports ◽  
2021 ◽  
Vol 37 (4) ◽  
pp. 109890
Author(s):  
Cassandra Sampaio-Baptista ◽  
Heather F. Neyedli ◽  
Zeena-Britt Sanders ◽  
Kata Diosi ◽  
David Havard ◽  
...  

Author(s):  
S. Heyden ◽  
M. Ortiz

We investigate the functional optimality of the cerebral cortex of an adult human brain geometry. Unlike most competing models, we postulate that the cerebral cortex formation is driven by the objective of maximizing the total information transmission rate. Starting from a random path model, we show that this optimization problem is related to the Steklov eigenvalue problem. Combining realistic brain geometries with the finite-element method, we calculate the underlying Steklov eigenvalues and eigenfunctions. By comparison to a convex hull approximation, we show that the adult human brain geometry indeed reduces the Steklov eigenvalue spectrum and thus increases the rate at which information is exchanged between points on the cerebral cortex. With a view to possible clinical applications, the leading Steklov eigenfunctions and the resulting induced magnetic fields are computed and reported.


2005 ◽  
Vol 53 (3) ◽  
pp. 385-390 ◽  
Author(s):  
Yuri B. Yurov ◽  
Ivan Y. Iourov ◽  
Viktor V. Monakhov ◽  
Ilia V. Soloviev ◽  
Viktor M. Vostrikov ◽  
...  

Despite the lack of direct cytogenetic studies, the neuronal cells of the normal human brain have been postulated to contain normal (diploid) chromosomal complement. Direct proof of a chromosomal mutation presence leading to large-scale genomic alterations in neuronal cells has been missing in the human brain. Large-scale genomic variations due to chromosomal complement instability in developing neuronal cells may lead to the variable level of chromosomal mosaicism probably having a substantial effect on brain development. The aim of the present study was the pilot assessment of chromosome complement variations in neuronal cells of developing and adult human brain tissues using interphase multicolor fluorescence in situ hybridization (mFISH). Chromosome-enumerating DNA probes from the original collection (chromosomes 1, 13 and 21, 18, X, and Y) were used for the present pilot FISH study. As a source of fetal brain tissue, the medulla oblongata was used. FISH studies were performed using uncultured fetal brain samples as well as organotypic cultures of medulla oblongata tissue. Cortex tissues of postmortem adult brain samples (Brodmann area 10) were also studied. In cultured in vitro embryonic neuronal brain cells, an increased level of aneuploidy was found (mean rate in the range of 1.3–7.0% per individual chromosome, in contrast to 0.6–3.0% and 0.1–0.8% in uncultured fetal and postmortem adult brain cells, respectively). The data obtained support the hypothesis regarding aneuploidy occurrence in normal developing and adult human brain.


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