Fate Mapping via Ms4a3-Expression History Traces Monocyte-Derived Cells

被引:427
作者
Liu, Zhaoyuan [1 ]
Gu, Yaqi [1 ]
Chakarov, Svetoslav [2 ]
Bleriot, Camille [2 ]
Kwok, Immanuel [2 ]
Chen, Xin [1 ]
Shin, Amanda [1 ]
Huang, Weijie [1 ]
Dress, Regine J. [2 ]
Dutertre, Charles-Antoine [2 ]
Schlitzer, Andreas [3 ]
Chen, Jinmiao [2 ]
Ng, Lai Guan [2 ]
Wang, Honglin [1 ]
Liu, Zhiduo [1 ]
Su, Bing [1 ,4 ]
Ginhoux, Florent [1 ,2 ,5 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Inst Immunol, Dept Immunol & Microbiol, Sch Med, Shanghai 200025, Peoples R China
[2] Agcy Sci Technol & Res, Singapore Immunol Network, Singapore 138648, Singapore
[3] Univ Bonn, LIMES Inst, Myeloid Cell Biol, D-53115 Bonn, Germany
[4] Shanghai Jiao Tong Univ, Key Lab Cell Differentiat & Apoptosis, Chinese Minist Educ, Sch Med, Shanghai 200025, Peoples R China
[5] SingHlth Duke NUS Acad Med Ctr, Translat Immunol Inst, Singapore, Singapore
基金
中国国家自然科学基金; 新加坡国家研究基金会;
关键词
PLASMACYTOID DENDRITIC CELLS; GENE-EXPRESSION; MACROPHAGES; TISSUE; PROGENITORS; REVEALS; LINEAGE; HETEROGENEITY; PRECURSORS; CX(3)CR1;
D O I
10.1016/j.cell.2019.08.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Most tissue-resident macrophage (RTM) populations are seeded by waves of embryonic hematopoiesis and are self-maintained independently of a bone marrow contribution during adulthood. A proportion of RTMs, however, is constantly replaced by blood monocytes, and their functions compared to embryonic RTMs remain unclear. The kinetics and extent of the contribution of circulating monocytes to RTM replacement during homeostasis, inflammation, and disease are highly debated. Here, we identified Ms4a3 as a specific gene expressed by granulocyte-monocyte progenitors (GMPs) and subsequently generated Ms4a3(TdT) reporter, Ms4a3(Cre), and Ms4a3(CreERT2) fate-mapping models. These models traced efficiently monocytes and granulocytes, but no lymphocytes or tissue dendritic cells. Using these models, we precisely quantified the contribution of monocytes to the RTM pool during homeostasis and inflammation. The unambiguous idenification of monocyte-derived cells will permit future studies of their function under any condition.
引用
收藏
页码:1509 / +
页数:36
相关论文
共 41 条
[1]   CX3CR1+ CD115+ CD135+ common macrophage/DC precursors and the role of CX3CR1 in their response to inflammation [J].
Auffray, Cedric ;
Fogg, Darin K. ;
Narni-Mancinelli, Emilie ;
Senechal, Brigitte ;
Trouillet, Celine ;
Saederup, Noah ;
Leemput, Julia ;
Bigot, Karine ;
Campisi, Laura ;
Abitbol, Marc ;
Molina, Thierry ;
Charo, Israel ;
Hume, David A. ;
Cumano, Ana ;
Lauvau, Gregoire ;
Geissmann, Frederic .
JOURNAL OF EXPERIMENTAL MEDICINE, 2009, 206 (03) :595-606
[2]   Long-lived self-renewing bone marrow-derived macrophages displace embryo-derived cells to inhabit adult serous cavities [J].
Bain, Calum C. ;
Hawley, Catherine A. ;
Garner, Hannah ;
Scott, Charlotte L. ;
Schridde, Anika ;
Steers, Nicholas J. ;
Mack, Matthias ;
Joshi, Anagha ;
Guilliams, Martin ;
Mowat, Allan Mc I. ;
Geissmann, Frederic ;
Jenkins, Stephen J. .
NATURE COMMUNICATIONS, 2016, 7
[3]   Constant replenishment from circulating monocytes maintains the macrophage pool in the intestine of adult mice [J].
Bain, Calum C. ;
Bravo-Blas, Alberto ;
Scott, Charlotte L. ;
Perdiguero, Elisa Gomez ;
Geissmann, Frederic ;
Henri, Sandrine ;
Malissen, Bernard ;
Osborne, Lisa C. ;
Artis, David ;
Mowat, Allan Mci .
NATURE IMMUNOLOGY, 2014, 15 (10) :929-U236
[4]   Liver-Resident Macrophage Necroptosis Orchestrates Type 1 Microbicidal Inflammation and Type-2-Mediated Tissue Repair during Bacterial Infection [J].
Bleriot, Camille ;
Dupuis, Theo ;
Jouvion, Gregory ;
Eberl, Gerard ;
Disson, Olivier ;
Lecuit, Marc .
IMMUNITY, 2015, 42 (01) :145-158
[5]   Two distinct interstitial macrophage populations coexist across tissues in specific subtissular niches [J].
Chakarov, Svetoslav ;
Lim, Hwee Ying ;
Tan, Leonard ;
Lim, Sheau Yng ;
See, Peter ;
Lum, Josephine ;
Zhang, Xiao-Meng ;
Foo, Shihui ;
Nakamizo, Satoshi ;
Duan, Kaibo ;
Kong, Wan Ting ;
Gentek, Rebecca ;
Balachander, Akhila ;
Carbajo, Daniel ;
Bleriot, Camille ;
Malleret, Benoit ;
Tam, John Kit Chung ;
Baig, Sonia ;
Shabeer, Muhammad ;
Toh, Sue-Anne Ee Shiow ;
Schlitzer, Andreas ;
Larbi, Anis ;
Marichal, Thomas ;
Malissen, Bernard ;
Chen, Jinmiao ;
Poidinger, Michael ;
Kabashima, Kenji ;
Bajenoff, Marc ;
Ng, Lai Guan ;
Angeli, Veronique ;
Ginhoux, Florent .
SCIENCE, 2019, 363 (6432) :1190-+
[6]   Conditional gene targeting in macrophages and granulocytes using LysMcre mice [J].
Clausen, BE ;
Burkhardt, C ;
Reith, W ;
Renkawitz, R ;
Förster, I .
TRANSGENIC RESEARCH, 1999, 8 (04) :265-277
[7]   Human HTm4 is a hematopoietic cell cycle regulator [J].
Donato, JL ;
Ko, J ;
Kutok, JL ;
Cheng, T ;
Shirakawa, T ;
Mao, XQ ;
Beach, D ;
Scadden, DT ;
Sayegh, MH ;
Adra, CN .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 109 (01) :51-58
[8]   Plasmacytoid dendritic cells develop from Ly6D+ lymphoid progenitors distinct from the myeloid lineage [J].
Dress, Regine J. ;
Dutertre, Charles-Antoine ;
Giladi, Amir ;
Schlitzer, Andreas ;
Low, Ivy ;
Shadan, Nurhidaya Binte ;
Tay, Alicia ;
Lum, Josephine ;
Kairi, Muhammad Faris Bin Mohd ;
Hwang, You Yi ;
Becht, Etienne ;
Cheng, Yang ;
Chevrier, Marion ;
Larbi, Anis ;
Newell, Evan W. ;
Amit, Ido ;
Chen, Jinmiao ;
Ginhoux, Florent .
NATURE IMMUNOLOGY, 2019, 20 (07) :852-+
[9]   Self-renewing resident arterial macrophages arise from embryonic CX3CR1+ precursors and circulating monocytes immediately after birth [J].
Ensan, Sherine ;
Li, Angela ;
Besla, Rickvinder ;
Degousee, Norbert ;
Cosme, Jake ;
Roufaiel, Mark ;
Shikatani, Eric A. ;
El-Maldizil, Mahmoud ;
Williams, Jesse W. ;
Robins, Lauren ;
Li, Cedric ;
Lewis, Bonnie ;
Yun, Tae Jin ;
Lees, Jun Seong ;
Wieghofer, Peter ;
Khattar, Ramzi ;
Farrokhil, Kaveh ;
Byrne, John ;
Ouzounian, Maral ;
Zavitz, Caleb C. J. ;
Levy, Gary A. ;
Bauer, Carla M. T. ;
Libby, Peter ;
Husain, Mansoor ;
Swirski, Filip K. ;
Cheong, Cheolho ;
Prinz, Marco ;
Hilgendorf, Ingo ;
Randolph, Gwendalyn J. ;
Epelman, Slava ;
Gramolini, Anthony O. ;
Cybulsky, Myron I. ;
Rubin, Barry B. ;
Robbins, Clinton S. .
NATURE IMMUNOLOGY, 2016, 17 (02) :159-168
[10]   Regulation of Cre recombinase activity by mutated estrogen receptor ligand-binding domains [J].
Feil, R ;
Wagner, J ;
Metzger, D ;
Chambon, P .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 237 (03) :752-757