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. 2017 Apr 5;129(20):2749–2759. doi: 10.1182/blood-2017-01-761643

Figure 5.

Figure 5.

IL-6 and APRIL in concert with CD138 expression promote ASC survival. (A-E) Purified transgenic B cells from WT and sdc1−/− mice were injected into host mice in which the hematopoietic cells were either WT, IL-6 deficient (IL-6−/−), or APRIL deficient (APRIL−/−), and immunized and examined for YFP+ ASCs on day 7. (A) Graph depicts the percentage of WT and sdc1−/− ASCs from the LN in the different host mice. (B) WT ASCs were examined for apoptosis by Annexin V staining. Representative contour plots are shown (left). Graph depicts percentage of apoptosis in the CD138+ compartment of WT ASCs in WT, IL-6−/−, or APRIL−/− hosts. (C) As in Figure 3H, intravital two-photon microscopy was performed on the surgically exposed popliteal LNs of immunized mice. Apoptotic events were recorded and quantified in a blinded manner. Graph represents the number of apoptotic events observed per hour. (D-E) WT and sdc1−/− ASCs from the LN in the different host mice were examined for intracellular expression of Bcl-2 (D) and Mcl-1 (E). Graphs depict the MFI. *P < .05; **P < .01. ns, not significant.