Macrophage core program | Nature Immunology

Macrophage core program | Nature Immunology

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Access through your institution Buy or subscribe The mechanisms that control the diversification of tissue-resident macrophages remain unclear. In _Science_, Geissmann and colleagues perform spatio-temporal analysis of macrophage development in mice. Transcriptional profiling of embryonic erythro-myeloid progenitors, fetal CD45+Lin−c-kit− pre-macrophages and F4/80+ adult tissue macrophages identifies a core macrophage transcriptional program, including expression of the transcription-factor-encoding genes _Csf1r_, _Maf_, _Batf3_, _Pparg_, _Irf8_ and _Zeb2_, that is acquired in pre-macrophages as they colonize the embryo in a manner dependent on the chemokine receptor CX3CR1. Tissue-specific signatures are acquired in each population as early as embryonic day 12.5 in microglia, Kupffer cells and kidney macrophages or undergo postnatal changes in Langerhans cells and alveolar macrophages. Genes encoding some tissue-specific factors are expressed as early as embryonic day 10.26 in tissue macrophages (_Sall1_ and _Sall3_) or are expressed in erythro-myeloid progenitors or pre-macrophages (_Id1_ and _Sall3_) before their expression becomes restricted to a certain macrophage subset. The transcription factor Id3 emerges as being important for the development and maintenance of Kupffer cells. _Science_ (4 August 2016) doi:10.1126/science.aaf4238 This is a preview of subscription content, access via your institution ACCESS OPTIONS Access through your institution Subscribe to this journal Receive 12 print issues and online access $209.00 per year only $17.42 per issue Learn more Buy this article * Purchase on SpringerLink * Instant access to full article PDF Buy now Prices may be subject to local taxes which are calculated during checkout ADDITIONAL ACCESS OPTIONS: * Log in * Learn about institutional subscriptions * Read our FAQs * Contact customer support Authors * Ioana Visan View author publications You can also search for this author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Visan, I. Macrophage core program. _Nat Immunol_ 17, 1141 (2016). https://doi.org/10.1038/ni.3569 Download citation * Published: 20 September 2016 * Issue Date: October 2016 * DOI: https://doi.org/10.1038/ni.3569 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative

Access through your institution Buy or subscribe The mechanisms that control the diversification of tissue-resident macrophages remain unclear. In _Science_, Geissmann and colleagues perform


spatio-temporal analysis of macrophage development in mice. Transcriptional profiling of embryonic erythro-myeloid progenitors, fetal CD45+Lin−c-kit− pre-macrophages and F4/80+ adult tissue


macrophages identifies a core macrophage transcriptional program, including expression of the transcription-factor-encoding genes _Csf1r_, _Maf_, _Batf3_, _Pparg_, _Irf8_ and _Zeb2_, that


is acquired in pre-macrophages as they colonize the embryo in a manner dependent on the chemokine receptor CX3CR1. Tissue-specific signatures are acquired in each population as early as


embryonic day 12.5 in microglia, Kupffer cells and kidney macrophages or undergo postnatal changes in Langerhans cells and alveolar macrophages. Genes encoding some tissue-specific factors


are expressed as early as embryonic day 10.26 in tissue macrophages (_Sall1_ and _Sall3_) or are expressed in erythro-myeloid progenitors or pre-macrophages (_Id1_ and _Sall3_) before their


expression becomes restricted to a certain macrophage subset. The transcription factor Id3 emerges as being important for the development and maintenance of Kupffer cells. _Science_ (4


August 2016) doi:10.1126/science.aaf4238 This is a preview of subscription content, access via your institution ACCESS OPTIONS Access through your institution Subscribe to this journal


Receive 12 print issues and online access $209.00 per year only $17.42 per issue Learn more Buy this article * Purchase on SpringerLink * Instant access to full article PDF Buy now Prices


may be subject to local taxes which are calculated during checkout ADDITIONAL ACCESS OPTIONS: * Log in * Learn about institutional subscriptions * Read our FAQs * Contact customer support


Authors * Ioana Visan View author publications You can also search for this author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS


ARTICLE Visan, I. Macrophage core program. _Nat Immunol_ 17, 1141 (2016). https://doi.org/10.1038/ni.3569 Download citation * Published: 20 September 2016 * Issue Date: October 2016 * DOI:


https://doi.org/10.1038/ni.3569 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently


available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative