# Evaluation of the Osteogenic Potential of Apigenin via Inducing Autophagy: An In Vitro Study

**Authors:** Mozafar Khazaei, Amirmohammad Khodaei, Maryam Bozorgi, Mohammad Rasool Khazaei, Azam Bozorgi

PMC · DOI: 10.1155/sci/6446943 · 2026-02-12

## TL;DR

This study shows that apigenin boosts bone cell development in stem cells by triggering autophagy, a process that helps cells renew.

## Contribution

The novel finding is that apigenin enhances osteogenic differentiation of ASCs through autophagy induction.

## Key findings

- Apigenin treatment increased expression of osteogenic and autophagy-related genes and proteins in ASCs.
- Alkaline phosphatase activity and calcium deposition were significantly higher in apigenin-treated groups.
- Apigenin promotes osteogenic differentiation of ASCs via autophagy stimulation.

## Abstract

The present study aimed to evaluate the effect of apigenin (Api) on the osteogenic differentiation of adipose tissue‐derived mesenchymal stem cells (ASCs) by stimulating autophagy. ASCs were isolated from fresh adipose tissues using mechanical and enzymatic digestion and characterized using flow cytometry. ASCs were treated with Api (0, 5, 10, 25, and 50 µM) for 48 and 72 h. After determining the optimal doses of Api (5 and 10 µM), ASCs were differentiated into the osteogenic lineage for 7 and 21 days. The expression of osteogenic and autophagy genes and proteins, as well as alkaline phosphatase (ALP) activity and calcium deposition, were assessed. About 94% of ASCs expressed CD73, CD90, and CD105, while 99% didn’t express CD34 and CD45. Api treatment increased the expression of ALP, RUNX2, COL I, osteocalcin (OCN), ATG5, ATG7, and LC3A genes, and RUNX2, OCN, LC3‐1, and LC3‐II proteins dose‐dependently. ALP activity and calcium deposition were significantly higher in Api‐treated groups than in the control. Api increased the osteogenic differentiation of ASCs via inducing autophagy, an effect advantageous for enhancing SC differentiation efficiency.

## Linked entities

- **Genes:** ALPP (alkaline phosphatase, placental) [NCBI Gene 250], RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860], bglap2 (bone gamma-carboxyglutamate (gla) protein (osteocalcin) 2) [NCBI Gene 100493875], BGLAP (bone gamma-carboxyglutamate protein) [NCBI Gene 632], ATG5 (autophagy related 5) [NCBI Gene 9474], ATG7 (autophagy related 7) [NCBI Gene 10533], MAP1LC3A (microtubule associated protein 1 light chain 3 alpha) [NCBI Gene 84557], Map1lc3a (microtubule-associated protein 1 light chain 3 alpha) [NCBI Gene 362245]
- **Proteins:** RUNX2 (RUNX family transcription factor 2), BGLAP (bone gamma-carboxyglutamate protein), Map1lc3a (microtubule-associated protein 1 light chain 3 alpha)
- **Chemicals:** apigenin (PubChem CID 5280443)

## Full-text entities

- **Genes:** NT5E (5'-nucleotidase ecto) [NCBI Gene 4907] {aka CALJA, CD73, E5NT, NT, NT5, NTE}, PTPRC (protein tyrosine phosphatase receptor type C) [NCBI Gene 5788] {aka B220, CD45, CD45R, GP180, IMD105, L-CA}, ATG7 (autophagy related 7) [NCBI Gene 10533] {aka APG7-LIKE, APG7L, GSA7, SCAR31}, ATG5 (autophagy related 5) [NCBI Gene 9474] {aka APG5, APG5-LIKE, APG5L, ASP, SCAR25, hAPG5}, BGLAP (bone gamma-carboxyglutamate protein) [NCBI Gene 632] {aka BGP, OC, OCN}, ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860] {aka AML3, CBF-alpha-1, CBFA1, CCD, CCD1, CLCD}, THY1 (Thy-1 cell surface antigen) [NCBI Gene 7070] {aka CD90, CDw90}, CD34 (CD34 molecule) [NCBI Gene 947], MAP1LC3A (microtubule associated protein 1 light chain 3 alpha) [NCBI Gene 84557] {aka ATG8E, LC3, LC3A, MAP1ALC3, MAP1BLC3}
- **Chemicals:** Api (MESH:D047310), calcium (MESH:D002118)

## Figures

18 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12901651/full.md

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Source: https://tomesphere.com/paper/PMC12901651