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. 2011 Jan 4;121(2):613–622. doi: 10.1172/JCI44478

Figure 5. Mouse CD200hiItga6hi cell location, cell cycle status, and gene expression are similar to those of human CD200hiITGA6hi cells.

Figure 5

(A and B) As assessed by immunohistology of mouse skin, CD200 was expressed in bulge and secondary hair germ cells (A), whereas CD34 was expressed in bulge cells, but not secondary hair germ cells (B). (C) FACS identified a CD200hiItga6hi population. (D) CD200 versus CD34 identified bulge cells (CD200hiCD34+) and secondary hair germ cells (CD200hiCD34). (E) CD34hiItga6hi cells (Supplemental Figure 6E) overlaying CD200hiItga6hi cells (as in C) demonstrated that CD200hiItga6hi cells extended to a CD34 population, but CD34hiItga6hi cells were entirely CD200+. In F, only the CD200hiItga6hi population is shown, exhibiting overlap to the secondary hair germ. (G) Cell cycle analysis demonstrated the lowest frequency of G0/G1 in CD200hiItga6hi cells in the secondary hair germ (CD34; n = 3, P = 0.02). (H) Enriched gene lists from microarray expression analysis of human CD200hiITGA6hi, mouse bulge (CD200hiCD34+), and mouse secondary hair germ (CD200hiCD34) cells demonstrated that the human CD200hiITGA6hi population overlapped with both mouse populations, but more so with murine bulge than with murine secondary hair germ. Scale bars: 100 μm. Numbers within dot plots indicate percent cells in the respective gate or quadrant.