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Status |
Public on Jun 07, 2023 |
Title |
Gene expression of Dcir-/- osteoclasts induced by M-CSF and RANKL |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Purpose: DCIR is an inhibitory type of C-type lectin receptor that regulates osteoclast (OC) formation and functions. This study aimed to find the genes of OCs that could be regulated through DCIR. Method: Bone marrow cells from WT and Dcir-/- mice were cultured in M-CSF for 2 days and the the cells were further cultured in M-CSF and RANKL. RNA profiles were generated by deep sequencing, in triplicate, using Illumina NovaSeq. Results: We detected xxx gense that were higher expression in Dcir-/- OCs, compared with WT OCs, with a fold change ≥1.5 and p value <0.05. Conclusion: Our data showed that Dcir deficiency in OCs changed the gene expression pattern, compared to WT OCs, which are induced by M-CSF and RANKL.
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Overall design |
mRNA profiles of WT and Dcir-/- osteoclasts for 2 days culture aftre RANKL stimulation
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Contributor(s) |
Shimizu K |
Citation(s) |
37266426 |
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Submission date |
Jan 21, 2023 |
Last update date |
Jun 07, 2023 |
Contact name |
Tomonori Kaifu |
E-mail(s) |
kaifu@tohoku-mpu.ac.jp
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Phone |
+817270212
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Organization name |
Tohoku Medicine and Pharmaceutical University
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Department |
Faculty of Medicine
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Lab |
Division of Immunology
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Street address |
1-15-1 Fukumuro Miyagino ku
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City |
Sendai |
State/province |
Miyagi |
ZIP/Postal code |
9838536 |
Country |
Japan |
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Platforms (1) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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Samples (6)
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Relations |
BioProject |
PRJNA926132 |