ScholarWorks@숙명여자대학교

초록

Following the publication of the original article [1], the authors found an error in Fig. 7B. Unintentionally, the wrong flow cytometry image was displayed in recruited CD8+ T cells toward APN KO BMSCs. To further verify the study's accuracy, we would like to provide the revised Fig. 7B. The correct image is presented in this correction article, and the correction does not change the description or the conclusion of the original paper. (Figure presented.) B APN KO BMSCs were placed in the bottom chamber, splenocytes from EL-4-bearing WT mice were placed in the upper chamber of the transwell plate, and the population of migrated CD8+ T cells in the bottom chamber was analyzed by flow cytometry. C Cell lysates from the BMSCs were used to measure the levels of various chemokines. All dots were quantified using ImageJ software, and bar graphs were used for quantitative data Further to this, the discussion has been updated to: “Indeed, APN activated GSK3β activity in BMSC (Fig. 4B), and the GSK3β inhibitor promoted the stabilization of HIF1α (Fig. 4D).” We offer the revised sentence to clarify the content of the research article. The authors would like to apologize for any inconvenience caused. The original article [1] has been corrected. © 2023, BioMed Central Ltd., part of Springer Nature.