A reader of JBMR contacted the journal with concerns of duplication with shifts and slight magnification in Fig. 5B in ref 1. The image appeared to show duplication of p38 MAPK staining, magnification adjustment, and enhanced brightness in the Comp(+) 6-hour image of Merge. The authors reported that they erroneously saved a sample image to the wrong folder, causing the duplication of PI image of p-p38 MAPK staining in Fig. 5B. 5 Fig (Figure presented.) Activation of ERK1/2 in osteocytes by compressive force loading. (A, B) Phosphorylation of ERK1/2 (A) and p38 MAPK (B) in loaded osteocytes. The loading period was 6 hours. Comp = compressive force loading. Arrowhead = osteocyte with nuclear translocation. Scale bars = 20mm. (C) Effects of PD98059 (left) and SB239063 (right) on osteocyte apoptosis induced by loading. The loading period was 6 hours. Each bar represents the means ± SE of three independent evaluations. *p<0.05, significantly different from control. The authors provided original and supplemental data for the editors and provided a corrected Fig. 5, shown below. The new Fig. 5A and B uses images of PI, ERK, p-ERK, p38 MAPK, p-p38 MAPK, and Merge, taken from samples for each group of Comp(-) 0 hours, Comp(-) 6 hours, and Comp(+) 6 hours during experiments at that time. Immunofluorescence staining in Fig. 5A and B showed that phosphorylation of ERK1/2 was promoted in loaded osteocytes (Fig. 5A), whereas phosphorylation of p38 MAPK was slightly enhanced after loading (Fig. 5B). There were some osteocytes showing nuclear translocation of p-ERK1/2. The authors confirmed that no revisions to the original text are needed.
ASJC Scopus subject areas
- Endocrinology, Diabetes and Metabolism
- Orthopedics and Sports Medicine