Dendritic cells in developing and adult zebrafish arise from different origins and display distinct <i>flt3</i> dependencies

Dendritic cells (DCs) are key cellular components of the immune system and perform crucial functions in innate and acquired immunity. In mammals, it is generally believed that DCs originate exclusively from hematopoietic stem cells (HSCs). Using a temporal-spatial resolved fate-mapping system, here we show that, in zebrafish, DCs arise from two sources: dorsal aorta-born endothelium-derived hematopoietic progenitors (EHPs) and HSCs. The EHP-derived DCs emerge early, predominantly colonizing the developing thymus during larval stages and diminishing by juvenile stages. In contrast, HSC-derived DCs emerge later and can populate different tissues from late larval stages to adulthood. We further document that the EHP- and HSC-derived DCs display different dependencies on Fms-like tyrosine kinase 3 (Flt3), a pivotal receptor tyrosine kinase crucial for DC development in mammals. Our study reveals the presence of two distinct waves of DC development in zebrafish, each with unique origins and developmental controls.

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Publication Details

Journal
Development
Published
2025-01-27
DOI
https://doi.org/10.1242/dev.204410
Citations
1
Primary Topic
Immunotherapy and Immune Responses
Type
article
Field-Weighted Citation Impact
0.80

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article

Dendritic cells in developing and adult zebrafish arise from different origins and display distinct flt3 dependencies

Zilong Wen, Guanzhen Lin, Youqi Wang, Thu Thao Pham
1 citations
Development
Immunotherapy and Immune Responses
0.80
article

Dendritic cells in developing and adult zebrafish arise from different origins and display distinct flt3 dependencies

Zilong Wen, Guanzhen Lin, Youqi Wang, Thu Thao Pham
article en
1 citations

Abstract

Dendritic cells (DCs) are key cellular components of the immune system and perform crucial functions in innate and acquired immunity. In mammals, it is generally believed that DCs originate exclusively from hematopoietic stem cells (HSCs). Using a temporal-spatial resolved fate-mapping system, here we show that, in zebrafish, DCs arise from two sources: dorsal aorta-born endothelium-derived hematopoietic progenitors (EHPs) and HSCs. The EHP-derived DCs emerge early, predominantly colonizing the developing thymus during larval stages and diminishing by juvenile stages. In contrast, HSC-derived DCs emerge later and can populate different tissues from late larval stages to adulthood. We further document that the EHP- and HSC-derived DCs display different dependencies on Fms-like tyrosine kinase 3 (Flt3), a pivotal receptor tyrosine kinase crucial for DC development in mammals. Our study reveals the presence of two distinct waves of DC development in zebrafish, each with unique origins and developmental controls.

DevelopmentVol. 152(4)
Hong Kong University of Science and Technology (HK), Southern University of Science and Technology (CN), Shenzhen Bay Laboratory (CN), University of Hong Kong (HK)
Research Grants Council, University Grants Committee
Openalex Percentile: Top 32%
Immunotherapy and Immune Responses
0.80
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