1. LAPTM5 is transactivated by RUNX2 and involved in RANKL trafficking in osteoblastic cells.
- Author
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Geng YM, Liu CX, Lu WY, Liu P, Yuan PY, Liu WL, Xu PP, and Shen XQ
- Subjects
- Animals, Biomarkers, Cell Line, Cells, Cultured, Coculture Techniques, Core Binding Factor Alpha 1 Subunit genetics, Gene Expression, Gene Expression Regulation, Immediate-Early Proteins metabolism, Membrane Proteins metabolism, Mice, Promoter Regions, Genetic, Protein Binding, Protein Transport, RANK Ligand genetics, Core Binding Factor Alpha 1 Subunit metabolism, Immediate-Early Proteins genetics, Membrane Proteins genetics, Osteoblasts metabolism, RANK Ligand metabolism, Transcriptional Activation
- Abstract
The present study aimed to investigate the role of lysosomal‑associated transmembrane protein 5 (LAPTM5) in osteoclast differentiation induced by osteoblasts. The results demonstrated that the expression levels of LAPTM5 were downregulated following runt‑related transcription factor 2 (RUNX2) silencing and upregulated following RUNX2 overexpression in ST2 cells. Chromatin immunoprecipitation analysis identified the binding of RUNX2 to the LAPTM5 promoter at the ‑1176 to ‑1171 position. Dual‑luciferase reporter assays confirmed that RUNX2 directly activated the LAPTM5 gene. The concentration of receptor activator of nuclear factor‑κB ligand (RANKL) protein in the cytoplasm and in the media was significantly increased following LAPTM5 knockdown. LAPTM5 silencing in ST2 cells enhanced osteoclastic differentiation of co‑cultured RAW264.7 cells. The present study indicated that expression of LAPTM5 was regulated by the interaction of RUNX2 with its promoter region and that LAPTM5 was involved in the trafficking of RANKL. These findings suggested a possible coupling mechanism between osteogenesis and osteoclastogenesis in which RUNX2 may be involved in osteoclast differentiation through the regulation of the lysosome‑associated genes that modulate RANKL expression.
- Published
- 2019
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