Open AccessTrim33 / Tif1-γ is essential for macrophage and neutrophil mobilisation to developmental or inflammatory cues
Author(s) -
Doris Lou Demy,
Muriel Tauzin,
Mylène Lancino,
Véronique Le Cabec,
Michael J. Redd,
Emi Murayama,
Isabelle MaridonneauParini,
Nikolaus S. Trede,
Philippe Herbomel
Publication year - 2017
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.203471
Subject(s) - biology , macrophage , microbiology and biotechnology , inflammation , immunology , genetics , in vitro
Macrophages infiltrate and establish in developing organs from an early stage, often before these have become vascularised. Similarly, leukocytes in general can quickly migrate through tissues to any site of wounding. This unique capacity is rooted in their characteristic amoeboid motility, the genetic basis of which is poorly known. Trim33 (Tif1-γ), a nuclear protein that associates with specific DNA binding transcription factors to modulate gene expression, has been found mainly involved in hematopoiesis and gene regulation by TGF-ß. Here we have discovered that in Trim33 deficient zebrafish embryos, primitive macrophages are unable to colonize the central nervous system to become microglia. Moreover, both macrophages and neutrophils of Trim33 deficient embryos display a reduced basal mobility within interstitial tissues, and a profound lack of response to inflammatory recruitment signals, including local bacterial infections. Correlatively, Trim33 deficient mouse bone marrow derived macrophages display a strongly reduced three-dimensional amoeboid mobility in fibrous collagen gels. The transcriptional regulator Trim33 is thus revealed as essential for the navigation of macrophages and neutrophils towards developmental or inflammatory cues within vertebrate tissues.