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. 2015 Apr 27;16(6):753–768. doi: 10.15252/embr.201439505

Figure 1.

Figure 1

Reduced LKB1 B-cell subsets with splenomegaly from a T-cell expansion in BKO-YFP mice
  1. Flow cytometry for YFP expression in CD19+ splenocytes from WT-YFP (= 7) and BKO-YFP (= 8) mice. ****= 4.9E-06 by two-tailed, unpaired Student's t-test.
  2. qRT–PCR (= 3) and a representative Western blot for LKB1 in YFP-sorted splenocytes from BKO-YFP mice. LKB1 expression, relative to 36b4 expression, shown normalized to LKB1+YPF CD19+ BKO B cells. ****= 3.8E-05 by two-tailed, unpaired Student's t-test.
  3. Flow cytometry analysis for splenic transitional (TR: CD19+B220+AA41+), follicular (FO: CD19+B220+AA41IgM+CD21+), and marginal zone (MZ: CD19+B220+AA41IgM++CD21++) B cells in WT (= 8) and BKO (= 11) mice and the percentage of YFP+ cells for each subpopulation in WT-YFP (= 7) and BKO-YFP (= 8) mice. *= 0.03 by Mann–Whitney U-test and ****= 3.5E-006 and 1.5E-010 by two-tailed, unpaired Student's t-test, respectively.
  4. Representative images of spleens from WT and BKO mice. Weight of WT (= 34) and BKO (= 34) spleens and cell numbers recovered from WT (= 13) and BKO (= 18) spleens. *P = 0.011 and ****= 9.7E-13 by two-tailed, unpaired Student's t-test.
  5. Flow cytometry and number of B220+CD19+ splenic B cells from WT (= 13) and BKO (= 18) mice.
  6. Flow cytometry and number of CD4+ and CD8+ T cells from WT (= 11) and BKO (= 11) mice. ****= 1.1E-06 and 4.6E-06, respectively, by Mann–Whitney U-test.
  7. Non-lymphocyte white blood cells in spleens calculated by flow cytometry from WT (= 5) and BKO (= 5) mice. **= 0.008, *= 0.03 and 0.032, respectively, by two-tailed, unpaired Student's t-test.
  8. Histologic sections of WT and BKO spleens stained with hematoxylin and eosin (H&E), anti-B220, or anti-CD3 antibodies. Scale bar represents 500 microns.
Data information: (A, C–G) Mean ± s.d. (B) Mean ± SEM.