Figure 1.
Figure 1. The differential responses of the patient's PBMCs are due to differential expression of NEMO in each lineage. (A) Defective response of the patient's PBMCs to LPS but not to IL-18. PBMCs from the patient and healthy controls were stimulated with varying doses of IL-18 plus IL-12 (20 ng/mL) or with varying doses of LPS plus IFN-γ (5000 U/mL). A representative of 2 consistent results is shown. (B) Western blotting analysis of NEMO. Fifty micrograms of PBMC cell lysates (lanes 1-3), HTLV-I-transformed cells (lanes 4-5), and EBV-transformed cells (lanes 6-7) from the patient (lanes 3, 5, and 7) and healthy controls (lanes 1, 2, 4, and 6) were used. β-actin was used as a control for equal loading (lanes 1-7).

The differential responses of the patient's PBMCs are due to differential expression of NEMO in each lineage. (A) Defective response of the patient's PBMCs to LPS but not to IL-18. PBMCs from the patient and healthy controls were stimulated with varying doses of IL-18 plus IL-12 (20 ng/mL) or with varying doses of LPS plus IFN-γ (5000 U/mL). A representative of 2 consistent results is shown. (B) Western blotting analysis of NEMO. Fifty micrograms of PBMC cell lysates (lanes 1-3), HTLV-I-transformed cells (lanes 4-5), and EBV-transformed cells (lanes 6-7) from the patient (lanes 3, 5, and 7) and healthy controls (lanes 1, 2, 4, and 6) were used. β-actin was used as a control for equal loading (lanes 1-7).

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