scholarly journals 31. GENETIC CONTROL OF DECONVOLVED BRAIN CELL-TYPES

2021 ◽  
Vol 51 ◽  
pp. e57
Author(s):  
Chloe Yap ◽  
Chongyuan Luo ◽  
Dorothea Seiler Vellame ◽  
Arjun Bhattacharya ◽  
Alice Franklin ◽  
...  
Cephalalgia ◽  
2018 ◽  
Vol 38 (13) ◽  
pp. 1976-1983 ◽  
Author(s):  
William Renthal

Background Migraine is a debilitating disorder characterized by severe headaches and associated neurological symptoms. A key challenge to understanding migraine has been the cellular complexity of the human brain and the multiple cell types implicated in its pathophysiology. The present study leverages recent advances in single-cell transcriptomics to localize the specific human brain cell types in which putative migraine susceptibility genes are expressed. Methods The cell-type specific expression of both familial and common migraine-associated genes was determined bioinformatically using data from 2,039 individual human brain cells across two published single-cell RNA sequencing datasets. Enrichment of migraine-associated genes was determined for each brain cell type. Results Analysis of single-brain cell RNA sequencing data from five major subtypes of cells in the human cortex (neurons, oligodendrocytes, astrocytes, microglia, and endothelial cells) indicates that over 40% of known migraine-associated genes are enriched in the expression profiles of a specific brain cell type. Further analysis of neuronal migraine-associated genes demonstrated that approximately 70% were significantly enriched in inhibitory neurons and 30% in excitatory neurons. Conclusions This study takes the next step in understanding the human brain cell types in which putative migraine susceptibility genes are expressed. Both familial and common migraine may arise from dysfunction of discrete cell types within the neurovascular unit, and localization of the affected cell type(s) in an individual patient may provide insight into to their susceptibility to migraine.


Glia ◽  
1991 ◽  
Vol 4 (4) ◽  
pp. 408-416 ◽  
Author(s):  
Susan Pearce-Kelling ◽  
William J. Mitchell ◽  
Brian A. Summers ◽  
Max J. G. Appel

1982 ◽  
Vol 109 (1) ◽  
pp. 78-82 ◽  
Author(s):  
Martin R. Harris ◽  
Nerina Harborne ◽  
Bryan J. Smith ◽  
James Allan

2020 ◽  
Vol 87 (9) ◽  
pp. S110 ◽  
Author(s):  
Frank Wendt ◽  
Gita Pathak ◽  
Todd Lencz ◽  
John Krystal ◽  
Joel Gelernter ◽  
...  

2019 ◽  
Vol 29 ◽  
pp. S1124
Author(s):  
Diogo Marinho Almeida ◽  
Samuel Demharter ◽  
Thomas Werge ◽  
Konstantin Khodosevich ◽  
Alfonso Demur

Author(s):  
Theodore A. Sarafian ◽  
M. Anthony Verity ◽  
Harry V. Vinters ◽  
Charles C.-Y. Shih ◽  
Liangru Shi ◽  
...  

Author(s):  
Leon Fodoulian ◽  
Joel Tuberosa ◽  
Daniel Rossier ◽  
Madlaina Boillat ◽  
Chenda Kan ◽  
...  

AbstractVarious reports indicate an association between COVID-19 and anosmia, suggesting an infection of the olfactory sensory epithelium, and thus a possible direct virus access to the brain. To test this hypothesis, we generated RNA-seq libraries from human olfactory neuroepithelia, in which we found substantial expression of the genes coding for the virus receptor angiotensin-converting enzyme-2 (ACE2), and for the virus internalization enhancer TMPRSS2. We analyzed a human olfactory single-cell RNA-seq dataset and determined that sustentacular cells, which maintain the integrity of olfactory sensory neurons, express ACE2 and TMPRSS2. We then observed that the ACE2 protein was highly expressed in a subset of sustentacular cells in human and mouse olfactory tissues. Finally, we found ACE2 transcripts in specific brain cell types, both in mice and humans. Sustentacular cells thus represent a potential entry door for SARS-CoV-2 in a neuronal sensory system that is in direct connection with the brain.


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