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A transcriptional network underlies the identity and diversity of tissue macrophages
Author(s) -
GAUTIER E
Publication year - 2014
Publication title -
acta ophthalmologica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.534
H-Index - 87
eISSN - 1755-3768
pISSN - 1755-375X
DOI - 10.1111/j.1755-3768.2014.1751.x
Subject(s) - biology , macrophage , mertk , adipose tissue macrophages , microbiology and biotechnology , gene expression , gene , adipose tissue , genetics , signal transduction , endocrinology , white adipose tissue , in vitro , receptor tyrosine kinase
We recently assessed gene expression in tissue macrophages, which do not derive from monocytes, extracted from various mouse organs and found that the diversity in gene expression among different populations of macrophages was considerable. Only a few hundred mRNA transcripts were selectively expressed by macrophages rather than dendritic cells, and many of these were not present in all macrophages. Nonetheless, well‐characterized surface markers, including MerTK and FcγR1 (CD64), along with a cluster of previously unidentified transcripts, were distinctly and universally associated with mature tissue macrophages. We further demonstrated how these transcripts and the proteins they encode facilitated distinguishing macrophages from dendritic cells, and showed that they were turned on during monocyte to inflammatory macrophage differentiation. Furthermore, in support of the high diversity observed among tissue resident macrophages, the mRNAs encoding several transcription factors were associated with single macrophage populations and we provided evidence that Pparg and Gata6 specifically controls the homeostasis of specific tissue resident macrophage populations.