|
Status |
Public on Jun 04, 2021 |
Title |
Endothelial cell infection and dysfunction, immune activation in severe COVID-19 |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
|
Summary |
SARS-CoV2 infects endothelial cells and induce the dysfunction of them.
|
|
|
Overall design |
I. We infected WT C57BL/6J or K18 hACE2 transegnic mice in both male and female mice with 2x10^5 pfu SARS-CoV2. Then those mice were eutanized 4 days post challenge and the lungs were removed and processed for total RNA preparation. II. We infected female WT C57BL/6J or K18 hACE2 transgenic mice with 2x10^5 pfu SARS-CoV2. Then those mice were eutanized 4 days post challenge and the lungs were removed and processed for single cell suspensions.
|
|
|
Contributor(s) |
Qin X, Kolls J |
Citation(s) |
34335981 |
NIH grant(s) |
Grant ID |
Grant title |
Affiliation |
Name |
U54 CA260581 |
Tulane University COVID Antibody and Immunity Network (TUCAIN) |
TULANE UNIVERSITY |
JAMES E Robinson |
|
Submission date |
Jun 02, 2021 |
Last update date |
Aug 01, 2023 |
Contact name |
Jay Kolls |
Organization name |
Tulane University
|
Department |
Medicine
|
Lab |
Center for Translational Research in Infection and Inflammation
|
Street address |
1430 Tulane Ave
|
City |
New Orleans |
State/province |
LA |
ZIP/Postal code |
70112 |
Country |
USA |
|
|
Platforms (2) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
GPL21626 |
NextSeq 550 (Mus musculus) |
|
Samples (8)
|
|
Relations |
BioProject |
PRJNA734526 |
SRA |
SRP322333 |