File:Mouse embryo Trafficking kinetics of CSF1R+ cells are similar to pre-macrophages.jpg

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Description Fig 5 (1 correction). Trafficking kinetics of CSF1R+ cells are similar to pre-macrophages. a Schematic graph for the Csf1rCre:Rosa26eYFP mouse model. b, e Fluorescence images of CSF1R YFP+ cells (green) in the YS (e) with corresponding quantifications (b) of cells per microscopic field at indicated time points; mean ± SD. c Quantification of intravascular CSF1R+ cells in an average-sized vessel; mean ± SD. d Velocity of intravascular non-adhering (n = 21) and rolling (n = 11) CSF1R+ cells in the YS at E9.5; median ± IQR. f, g Fluorescence images of CSF1R YFP+ cells (green) in different embryonic regions (f) with corresponding quantifications (g) of cells per microscopic field at indicated time points; ** p = 0.0072, n.s. p = 0.0569 (two-tailed Mann–Whitney test); median ± IQR. Scale bars are 100 µm (e, f)
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Source https://www.nature.com/articles/s41467-018-06065-9/figures/1 Yolk sac macrophage progenitors traffic to the embryo during defined stages of development. Nat Commun 9, 75 (2018). https://doi.org/10.1038/s41467-017-02492-2
Author Stremmel, C., Schuchert, R., Wagner, F. et al.
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current20:56, 21 April 2024Thumbnail for version as of 20:56, 21 April 20241,790 × 1,508 (1.34 MB)Rasbak (talk | contribs){{Information |description=Fig 5 (1 correction). Trafficking kinetics of CSF1R+ cells are similar to pre-macrophages. a Schematic graph for the Csf1r<sup>Cre</sup>:Rosa26<sup>eYFP</sup> mouse model. b, e Fluorescence images of CSF1R YFP+ cells (green) in the YS (e) with corresponding quantifications (b) of cells per microscopic field at indicated time points; mean ± SD. c Quantification of intravascular CSF1R+ cells in an average-sized vessel; mean ± SD. d Velocity of intravascular non-adheri...

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