GPR55 restrains IEL accumulation in the small intestine.

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Presentation transcript:

GPR55 restrains IEL accumulation in the small intestine. GPR55 restrains IEL accumulation in the small intestine. (A) Gpr55 transcript abundance in the indicated cell subsets relative to Hprt. Each point indicates cells sorted from an individual mouse (except for intestinal DCs and macrophages that were sorted from pooled samples of 10 mice), and lines indicate means ± SEM. EC, epithelial cell. (B) Flow cytometric analysis of CD8α and TCRγδ expression by small intestinal IELs from the indicated mice. Number shows fraction of cells in the indicated gate. (C) Frequency of IELs and LPLs (left and center) and number of IELs (right) in the indicated mice. Each population was pregated on CD45+CD3ε+ cells. Each point represents data from an individual mouse, and lines represent means ± SEM. Left: GPR55 Het, n = 20; GPR55 KO, n = 15. Center: GPR55 Het, n = 13; GPR55 KO, n = 9. Right: GPR55 Het, n = 16; GPR55 KO, n = 12. (D) Expression of Vγ7, Thy1.2, β7 integrin, and CD103 (αE integrin) on CD8α+CD8β− GL3+ IELs from GPR55 Het and KO mice. (E) Percentage of GL3+ cells among the CD4 and CD8 double-negative thymocyte population (left) and the fraction of these cells that express Vγ7 (right). GPR55 Het, n = 7; GPR55 KO, n = 4. (F) Frequency of IELs of the indicated types that had incorporated BrdU after a 1-week labeling period. GPR55 Het, n = 6; GPR55 KO, n = 5. (G) Number (left) and frequency (right) of IELs of the indicated types in irradiated WT mice reconstituted with GPR55 Het or KO BM. GPR55 Het, n = 4; GPR55 KO, n = 4. Data are representative of two independent experiments. (H) Ratio of GPR55 or empty vector (EV)–transduced cells compared with untransduced cells of the indicated types in BM chimeras reconstituted with GPR55 KO BM transduced with the indicated retroviral constructs. Thy1.1 marks transduced cells. **P < 0.01, *P < 0.05, n.s. (not significant). P > 0.05 by Student’s t test. Hayakazu Sumida et al. Sci. Immunol. 2017;2:eaao1135 Copyright © 2017 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works