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ZFIN ID: ZDB-PUB-170721-7
Trim33 / Tif1-γ is essential for macrophage and neutrophil mobilisation to developmental or inflammatory cues
Demy, D.L., Tauzin, M., Lancino, M., le Cabec, V., Redd, M., Murayama, E., Maridonneau-Parini, I., Trede, N., Herbomel, P.
Date: 2017
Source: Journal of Cell Science   130(17): 2797-2807 (Journal)
Registered Authors: Demy, Doris-Lou, Herbomel, Philippe, Lancino, Mylène, Murayama, Emi, Redd, Michael, Tauzin, Muriel, Trede, Nick
Keywords: Amoeboid motility, In vivo, Leukocyte recruitment, Macrophages, Neutrophils, Tif1-gamma, Trim33, Zebrafish
MeSH Terms:
  • Animals
  • Bacterial Infections/pathology
  • Bone Marrow Cells/metabolism
  • Cell Movement
  • Central Nervous System/metabolism
  • Central Nervous System/pathology
  • Inflammation/metabolism
  • Inflammation/pathology*
  • Macrophages/metabolism*
  • Mice
  • Microglia/metabolism
  • Mutation/genetics
  • Myeloid Cells/metabolism
  • Neutrophils/metabolism*
  • Retina/pathology
  • Transcription Factors/deficiency
  • Transcription Factors/genetics
  • Transcription Factors/metabolism*
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism
PubMed: 28724755 Full text @ J. Cell Sci.
FIGURES
ABSTRACT
Macrophages infiltrate and establish in developing organs from an early stage, often before these have become vascularized. 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 understood. Trim33 (also known as Tif1-γ), a nuclear protein that associates with specific DNA-binding transcription factors to modulate gene expression, has been found to be mainly involved in hematopoiesis and gene regulation mediated by TGF-β. 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 a 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 being essential for the navigation of macrophages and neutrophils towards developmental or inflammatory cues within vertebrate tissues.
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