Skip to main content
. Author manuscript; available in PMC: 2021 Apr 6.
Published in final edited form as: Nat Immunol. 2021 Mar 11;22(4):510–519. doi: 10.1038/s41590-021-00894-5

Extended Data Fig. 4. Fate-mapping of perivascular lymphoid tissue organizer cells.

Extended Data Fig. 4

a, Schematic description of fate-mapping experiments in Ccl19 iBbw2.1 mice. Pregnant mice were treated with Doxycyclin (Dox) at embryonic day (E) 18.5 and offsprings were analysed at indicated timepoints. b, Images showing PP anlage at E18.5 harvested from Ccl19 iBbw2.1 embryos. Dashed line indicates intestinal epithelium. c, Images showing PP anlagen at postnatal day (P) 1 and P4 (in d) harvested from Ccl19 iBbw2.1 pups kept on Dox since E18.5. Arrowheads indicate perivascular EYFP+ cell cluster. e, Images showing PP anlage at P7 harvested from Ccl19 1Bbw2.1 pups kept on Dox since E18.5. Boxed area indicates representative area of higher magnification images below, Arrowheads indicate EYFP+ cell cluster. f, Images show whole-mount analysis of adult PP from Ccl19 1Bbw2.1mice, which were kept without (w/o) Dox. g, Images depicting histological section of adult PP harvested from Ccl19 1Bbw2.1mice kept on doxycycline since E18.5. h, Images showing high resolution confocal analysis of EYFP+ and tdTOMATO+ cell clusters in PP from adult Ccl19 iBbw2.1 mice kept on Dox since E18.5.Scale bars, 20 μm (b,c), 50 μm (d), 100 μm (e), 500 μm (f,g), 10 μm (h). Images are representative of at least 3 mice from 2-3 independent experiments.