Transitional premonocytes emerge in the periphery for host defense against bacterial infections

Author:

Teh Ye Chean12ORCID,Chooi Ming Yao13ORCID,Liu Dehua1ORCID,Kwok Immanuel1ORCID,Lai Ghee Chuan1ORCID,Ayub Ow Yong Liyana34ORCID,Ng Melissa1ORCID,Li Jackson L. Y.1ORCID,Tan Yingrou15ORCID,Evrard Maximilien1ORCID,Tan Leonard13ORCID,Liong Ka Hang1ORCID,Leong Keith1ORCID,Goh Chi Ching1ORCID,Chan Andrew Y. J.1ORCID,Shadan Nurhidaya Binte1ORCID,Mantri Chinmay Kumar6ORCID,Hwang You Yi1ORCID,Cheng Hui7ORCID,Cheng Tao7ORCID,Yu Weimiao8ORCID,Tey Hong Liang359ORCID,Larbi Anis1,St John Ashley36ORCID,Angeli Veronique3ORCID,Ruedl Christiane10ORCID,Lee Bernett1ORCID,Ginhoux Florent111ORCID,Chen Swaine L.34ORCID,Ng Lai Guan13710ORCID,Ding Jeak Ling2ORCID,Chong Shu Zhen1ORCID

Affiliation:

1. Singapore Immunology Network (SIgN), A*STAR (Agency for Science, Technology and Research), Biopolis, Singapore 138648, Singapore.

2. Department of Biological Science, National University of Singapore (NUS), Singapore 117543, Singapore.

3. Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117545, Singapore.

4. Genome Institute of Singapore, A*STAR (Agency for Science, Technology and Research), Biopolis, Singapore 138672, Singapore.

5. National Skin Centre, 1 Mandalay Road, Singapore 308205, Singapore.

6. Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore 169857, Singapore.

7. State Key Laboratory of Experimental Hematology, National Clinical Research Centre for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China.

8. Institute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), Singapore 138673, Singapore.

9. Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore 308232, Singapore.

10. School of Biological Sciences, Nanyang Technological University, Singapore 637551, Singapore.

11. Shanghai Institute of Immunology, Shanghai JiaoTong University School of Medicine, Shanghai 200025, China.

Abstract

Circulating Ly6Chimonocytes often undergo cellular death upon exhaustion of their antibacterial effector functions, which limits their capacity for subsequent macrophage differentiation. This shrouds the understanding on how the host replaces the tissue-resident macrophage niche effectively during bacterial invasion to avert infection morbidity. Here, we show that proliferating transitional premonocytes (TpMos), an immediate precursor of mature Ly6Chimonocytes (MatMos), were mobilized into the periphery in response to acute bacterial infection and sepsis. TpMos were less susceptible to apoptosis and served as the main source of macrophage replenishment when MatMos were vulnerable toward bacteria-induced cellular death. Furthermore, TpMo and its derived macrophages contributed to host defense by balancing the proinflammatory cytokine response of MatMos. Consequently, adoptive transfer of TpMos improved the survival outcome of lethal sepsis. Our findings hence highlight a protective role for TpMos during bacterial infections and their contribution toward monocyte-derived macrophage heterogeneity in distinct disease outcomes.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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