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Status |
Public on May 27, 2022 |
Title |
Next Generation Sequencing of transcriptomes to reveal the role of HDAC3 in regulating the development of LMPP and CD115- CDP and bone marrow pDCs |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Hdac3 is highly expressed in pDCs, and its deficiency led to substantially impaired development of pDCs, but not cDCs in bone marrow (BM) and spleen. Meanwhile, the hematopoietic progenitors with DC differentiation potential, including CMP, CLP and CD115+ CDP were significantly decreased. Although the number of HSC and CD115− CDP were increased, their differentiation potential toward pDCs were abolished. Further investigation demonstrated that HDAC3 was required for the differentiation of pDC from progenitors at different differentiation stages.
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Overall design |
RNA profiles of sorted control or HDAC3 knockout mouse LMPPs and CD115- CDPs and bone marrow pDCs cells
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Contributor(s) |
Wu L, Zhang Y, He Z |
Citation(s) |
38011375 |
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Submission date |
Feb 22, 2022 |
Last update date |
Jan 02, 2024 |
Contact name |
Zhimin He |
E-mail(s) |
hzhm_2007@126.com
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Phone |
86-18010073801
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Organization name |
Tsinghua University
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Department |
School of Medicine
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Street address |
No. 1 Qinghuayuan Street
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City |
Beijing |
ZIP/Postal code |
100084 |
Country |
China |
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Platforms (2) |
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Samples (12)
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Relations |
BioProject |
PRJNA809366 |