<scp>D</scp> 2‐type dopamine receptors are required for <scp>LPS</scp> ‐induced acute hematopoiesis

Hematopoietic stem and progenitor cells (HSPCs) rapidly proliferate during infection and stress to replenish immune cells, which is essential for host defense. Dopamine, released by bone marrow (BM) nerves, regulates HSPCs via D2-type dopamine receptors. However, their role in emergency hematopoiesis across organs is unclear. We show that D2-type receptors are crucial for hematopoiesis in BM, spleen, lymph nodes, and thymus. Genetic deletion of D2-type receptors in hematopoietic cells (DKO<sup>∆HC</sup>) impairs HSPC proliferation and reduces blood cell production under lipopolysaccharide (LPS) stimulation, particularly in BM and spleen. Limited defects are observed in lymphoid organs. Mechanistically, D2-type signaling modulates the LPS-activated TAK1-ERK pathway via Lck. The inhibition of Lck mimics decreased ERK phosphorylation seen in DKO<sup>∆HC</sup> HSPCs, revealing the important role of dopamine signals in LPS-TLR4-mediated responses.

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Publication Details

Journal
FEBS Letters
Published
2025-08-11
DOI
https://doi.org/10.1002/1873-3468.70143
Primary Topic
Hematological disorders and diagnostics
Type
article
Field-Weighted Citation Impact
0.00

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article

D 2‐type dopamine receptors are required for LPS ‐induced acute hematopoiesis

Jinjin Ma, Tao‐Sheng Li, Qi Chen, Zhao‐hua Deng et al.
FEBS Letters
Hematological disorders and diagnostics
article

D 2‐type dopamine receptors are required for LPS ‐induced acute hematopoiesis

Jinjin Ma, Tao‐Sheng Li, Qi Chen, Zhao‐hua Deng, Yang Liu, Yu Yu, Yuyan Li, Jiaxin Yang, Ke Bai
article en

Abstract

Hematopoietic stem and progenitor cells (HSPCs) rapidly proliferate during infection and stress to replenish immune cells, which is essential for host defense. Dopamine, released by bone marrow (BM) nerves, regulates HSPCs via D2-type dopamine receptors. However, their role in emergency hematopoiesis across organs is unclear. We show that D2-type receptors are crucial for hematopoiesis in BM, spleen, lymph nodes, and thymus. Genetic deletion of D2-type receptors in hematopoietic cells (DKO<sup>∆HC</sup>) impairs HSPC proliferation and reduces blood cell production under lipopolysaccharide (LPS) stimulation, particularly in BM and spleen. Limited defects are observed in lymphoid organs. Mechanistically, D2-type signaling modulates the LPS-activated TAK1-ERK pathway via Lck. The inhibition of Lck mimics decreased ERK phosphorylation seen in DKO<sup>∆HC</sup> HSPCs, revealing the important role of dopamine signals in LPS-TLR4-mediated responses.

FEBS LettersVol. 599(22)
Guangzhou Institutes of Biomedicine and Health (CN), University of Chinese Academy of Sciences (CN), South China University of Technology (CN), Guangzhou Medical University (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences, Guangdong Provincial Pearl River Talents Program, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities, Science and Technology Planning Project of Guangdong Province, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Basic and Applied Basic Research Foundation of Guangdong Province
Good health and well-being
Openalex Percentile: Top 69%
Hematological disorders and diagnostics
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