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Updated: May 8, 2026

Identification and Isolation of Oligopotent and Lineage-committed Myeloid Progenitors from Mouse Bone Marrow
Published on: July 29, 2018
CpG oligodeoxynucleotide induces bone marrow precursor cells into myeloid-derived suppressor cells
Jie Chen1, Chengyu Deng, Qingmin Shi
1Department of Immunology, National Key Laboratory of Medical Immunology and Institute of Immunology, Second Military Medical University, Shanghai 200433, P.R. China.
CpG oligodeoxynucleotide (CpG ODN) stimulation inhibits dendritic cell (DC) development and promotes bone marrow precursor cell differentiation into myeloid-derived suppressor cells (MDSCs). This finding was observed in vitro and in Listeria monocytogenes-infected mice.
Area of Science:
- Immunology
- Cell Biology
Background:
- Dendritic cells (DCs) and myeloid-derived suppressor cells (MDSCs) play crucial roles in immune regulation.
- Standard methods for DC generation involve culturing mouse bone marrow (BM) cells with GM-CSF and IL-4.
- Previous work showed BM precursors differentiate into MDSCs when co-cultured with poly (I:C).
Purpose of the Study:
- To investigate the effect of CpG oligodeoxynucleotide (CpG ODN) on BM precursor cell differentiation.
- To determine if CpG ODN influences DC development and MDSC induction.
Main Methods:
- Mouse bone marrow precursor cells were cultured with GM-CSF and IL-4.
- Cultures were treated with CpG ODN.
- Cell populations were analyzed for markers and function.
- A similar model was studied in Listeria monocytogenes-infected mice.
Main Results:
- CpG ODN treatment led to the accumulation of Gr1+CD11b+ cells with MDSC functions.
- A similar accumulation of these cells was observed in mice infected with Listeria monocytogenes.
- Prolonged CpG ODN stimulation inhibited DC development.
Conclusions:
- CpG ODN can inhibit the development of dendritic cells.
- CpG ODN can induce the differentiation of bone marrow precursor cells into myeloid-derived suppressor cells.
- These findings have implications for understanding immune cell dynamics in response to microbial stimuli.
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