4.4 Article

Mechanism of Cyclic Tensile Stress in Osteogenic Differentiation of Human Periodontal Ligament Stem Cells

Journal

CALCIFIED TISSUE INTERNATIONAL
Volume 108, Issue 5, Pages 640-653

Publisher

SPRINGER
DOI: 10.1007/s00223-020-00789-x

Keywords

Cyclic tensile stress; Human periodontal ligament stem cells; Osteogenic differentiation; microRNA-129-5p; BMP2; smad pathway

Funding

  1. Guangdong Basic and Applied Basic Research Foundation [2019A1515110854]
  2. National Undergraduate Training Program for Innovation and Entrepreneurship of Sun Yat-sen University - Ministry of Education [201901113]

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The study found that cyclic tensile stress can enhance the osteogenic differentiation ability of human periodontal ligament stem cells (hPDLSCs) by regulating the expression levels of miR-129-5p and BMP2, and activating the BMP2/Smad signaling pathway. This stimulative effect is manifested by increased ALP activity, osteogenesis-related gene expression, mineralized nodules, and positive ALP staining.
Human periodontal ligament stem cells (hPDLSCs) can undergo osteogenic differentiation under induction conditions. Cyclic tensile stress (CTS) can stimulate stem cell osteogenic differentiation. The present study explored the mechanism of CTS in hPDLSC osteogenic differentiation. The hPDLSCs of the 4th passage were selected. hPDLSCs were subjected to CTS with deformation of 10% elongation at 0.5 Hz for 1, 4, 8, 12 and 24 h. ALP activity and staining, ARS staining and detection of expressions of osteogenesis-related genes (RUNX2, OPN, Sp7 and OCN) were used to assess hPDLSC osteogenic differentiation ability. microRNA (miR)-129-5p and BMP2 expression and p-Smad1/5 level were detected under CTS stimulation. The binding relationship between miR-129-5p and BMP2 was predicted and verified. The osteogenic differentiation ability of CTS-treated hPDLSCs was evaluated after intervention of miR-129-5p and BMP2. CTS induced hPDLSC osteogenic differentiation, as manifested by increased ALP activities, osteogenesis-related gene expressions and mineralized nodules, together with positive ALP staining. CTS inhibited miR-129-5p expression, and promoted BMP2 expression and p-Smad1/5 level in hPDLSCs. miR-129-5p targeted BMP2. Overexpressed miR-129-5p or silenced BMP2 prevented hPDLSC osteogenic differentiation ability. We demonstrated that CTS inhibited miR-129-5p expression, and then activated the BMP2/Smad pathway, thereby showing stimulative effects on hPDLSC osteogenic differentiation.

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