TY - JOUR
T1 - Origin and Heterogeneity of Tissue Myeloid Cells
T2 - A Focus on GMP-Derived Monocytes and Neutrophils
AU - Ng, Lai Guan
AU - Liu, Zhaoyuan
AU - Kwok, Immanuel
AU - Ginhoux, Florent
N1 - Publisher Copyright:
© 2023 Annual Reviews Inc.. All rights reserved.
PY - 2023/4/26
Y1 - 2023/4/26
N2 - Myeloid cells are a significant proportion of leukocytes within tissues, comprising granulocytes, monocytes, dendritic cells, and macrophages. With the identification of various myeloid cells that perform separate but complementary functions during homeostasis and disease, our understanding of tissue myeloid cells has evolved significantly. Exciting findings from transcriptomics profiling and fate-mapping mouse models have facilitated the identification of their developmental origins, maturation, and tissue-specific specializations. This review highlights the current understanding of tissue myeloid cells and the contributing factors of functional heterogeneity to better comprehend the complex and dynamic immune interactions within the healthy or inflamed tissue. Specifically, we discuss the new understanding of the contributions of granulocyte-monocyte progenitor-derived phagocytes to tissue myeloid cell heterogeneity as well as the impact of niche-specific factors on monocyte and neutrophil phenotype and function. Lastly, we explore the developing paradigm of myeloid cell heterogeneity during inflammation and disease.
AB - Myeloid cells are a significant proportion of leukocytes within tissues, comprising granulocytes, monocytes, dendritic cells, and macrophages. With the identification of various myeloid cells that perform separate but complementary functions during homeostasis and disease, our understanding of tissue myeloid cells has evolved significantly. Exciting findings from transcriptomics profiling and fate-mapping mouse models have facilitated the identification of their developmental origins, maturation, and tissue-specific specializations. This review highlights the current understanding of tissue myeloid cells and the contributing factors of functional heterogeneity to better comprehend the complex and dynamic immune interactions within the healthy or inflamed tissue. Specifically, we discuss the new understanding of the contributions of granulocyte-monocyte progenitor-derived phagocytes to tissue myeloid cell heterogeneity as well as the impact of niche-specific factors on monocyte and neutrophil phenotype and function. Lastly, we explore the developing paradigm of myeloid cell heterogeneity during inflammation and disease.
KW - GMP
KW - fate-mapping
KW - granulocyte-monocyte progenitors
KW - macrophages
KW - monocytes
KW - neutrophils
KW - niche
KW - tissue reprogramming
UR - http://www.scopus.com/inward/record.url?scp=85159255618&partnerID=8YFLogxK
U2 - 10.1146/annurev-immunol-081022-113627
DO - 10.1146/annurev-immunol-081022-113627
M3 - Review article
C2 - 37126421
AN - SCOPUS:85159255618
SN - 0732-0582
VL - 41
SP - 375
EP - 404
JO - Annual Review of Immunology
JF - Annual Review of Immunology
ER -