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. Author manuscript; available in PMC: 2010 Sep 23.
Published in final edited form as: Sci Signal. 2010 Mar 23;3(114):ra22. doi: 10.1126/scisignal.2000818

Fig. 4. Exaggerated Ca2+ signaling in human FAD B lymphoblasts.

Fig. 4

(A) Representative single cell Ca2+ responses to strong IgM stimulation (5µg/ml; arrow) in control human B lymphoblasts (CTL) or FAD lymphoblasts carrying PS1-A246E mutation. Dark lines below and to the left of each trace indicate zero Ca2+. (B) Responses to IgM stimulation. Percentages responding with Ca2+ oscillations (red) or large amplitude Ca2+ transients (blue). (C) Summary of peak amplitudes of high-amplitude transient Ca2+ responses triggered by 5 µg/ml anti-IgM. (D) Ca2+ oscillation frequency in response to anti-IgM. N = 3 experiments with 30 cells in each. Asterisk: p < 0.05, Student’s t-test. (E) Representative single cell Ca2+ responses to weak IgM stimulation (50 ng/ml; arrow) and (F) spontaneous oscillations during perfusion with serum-containing medium in lymphoblasts from unaffected (CTL) and FAD individuals. Dark lines: zero Ca2+ level. (G) Percentage of cells responding to IgM (black) or undergoing spontaneous Ca2+ oscillations in complete medium (blue). (H) Summaries of Ca2+ oscillation frequency in response to IgM (black) or spontaneous Ca2+ oscillations observed in complete medium (blue). Data in each group summarized from 4 experiments with 30 cells in each. Asterisks or #: p < 0.05 by ANOVA as compared with respective controls.