Fig. 4. Induction of eotaxin mRNA expression in normal human dermal fibroblasts. Northern blot analysis of total RNA (10 μg) isolated from fibroblasts. Blots were hybridized with eotaxin- and subsequently with GAPDH-specific probes. (A) Untreated fibroblasts (lane 1), fibroblasts after stimulation with 30 ng/mL TNF- (lane 2), and fibroblasts after cocultivation with the Hodgkin cell lines L1236 (lane 3), L428 (lane 4), KM-H2 (lane 5), and the pre-B–cell line Blin-1 (lane 6). (B) Fibroblasts after stimulation with 10 ng/mL TNF- (lanes 1 and 2) and incubation with anti–TNF- antibodies (lane 2). Fibroblasts after cultivation in supernatant of the Hodgkin cell line L1236 (lanes 3 and 4) and incubation with anti–TNF- antibodies (lane 4).
Fig. 4.

Induction of eotaxin mRNA expression in normal human dermal fibroblasts. Northern blot analysis of total RNA (10 μg) isolated from fibroblasts. Blots were hybridized with eotaxin- and subsequently with GAPDH-specific probes. (A) Untreated fibroblasts (lane 1), fibroblasts after stimulation with 30 ng/mL TNF- (lane 2), and fibroblasts after cocultivation with the Hodgkin cell lines L1236 (lane 3), L428 (lane 4), KM-H2 (lane 5), and the pre-B–cell line Blin-1 (lane 6). (B) Fibroblasts after stimulation with 10 ng/mL TNF- (lanes 1 and 2) and incubation with anti–TNF- antibodies (lane 2). Fibroblasts after cultivation in supernatant of the Hodgkin cell line L1236 (lanes 3 and 4) and incubation with anti–TNF- antibodies (lane 4).

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