Merck
CN
  • Kaempferol promotes proliferation, migration and differentiation of MC3T3-E1 cells via up-regulation of microRNA-101.

Kaempferol promotes proliferation, migration and differentiation of MC3T3-E1 cells via up-regulation of microRNA-101.

Artificial cells, nanomedicine, and biotechnology (2019-04-04)
Yang Wang, Hongyu Chen, Hanyang Zhang
摘要

Osteoblast has been found to exert indispensable functions during fracture healing. This study aimed to investigate the effects of kaempferol, a natural flavonoid compound, on osteoblast proliferation, migration and differentiation, as well as possible molecular mechanisms. qRT-PCR was performed to measure the expression level of microRNA-101 (miR-101). Cell viability and migration were respectively assessed using cell counting kit-8 (CCK-8) assay and two-chamber migration assay. Relative alkaline phosphatase (ALP) activity was evaluated using p-nitrophenyl phosphate (pNPP) as substrate. Western blotting was used to detect the protein expression levels of key molecules involved in cell proliferation, migration, differentiation, and Wnt/β-catenin pathway. Kaempferol treatment significantly promoted MC3T3-E1 cell proliferation, migration, and differentiation. Mechanistically, kaempferol notably enhanced the expression level of miR-101 in MC3T3-E1 cells. Knockdown of miR-101 obviously weakened the promoting effects of kaempferol on MC3T3-E1 cell proliferation, migration, and differentiation. In addition, kaempferol remarkably activated Wnt/β-catenin pathway in MC3T3-E1 cells via up-regulating miR-101. This research further confirmed the promoting effects of kaempferol on osteoblast proliferation, migration, and differentiation. The up-regulation of miR-101 and activation of Wnt/β-catenin pathway caused by kaempferol play critical roles in the promoting effects of kaempferol on osteoblast proliferation, migration, and differentiation.

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Sigma-Aldrich
叶酸, ≥97%
Sigma-Aldrich
山柰酚, ≥97.0% (HPLC)
Sigma-Aldrich
QCM趋化细胞迁移分析,24孔(8 µm),比色法, The QCM 24-well Migration Assay is ideal for the study of chemotaxis cell migration. The assay uses a 24-well plate with an 8 micron pore size, with colorimetric detection.