# A 3D Collagen–Alginate Hydrogel Model for Mechanoregulation of Autophagy in Periodontal Ligament Cells

**Authors:** Xueping Kang, Bei Gao, Tong Wang, Qingbo Zhao, Shiyang Wu, Chuqi Li, Hui Zhang, Rui Zou, Yijie Wang

PMC · DOI: 10.3390/gels12010091 · 2026-01-20

## TL;DR

This paper introduces a 3D hydrogel model to study how mechanical compression affects autophagy in periodontal ligament cells, revealing a key role for AKT-mTOR signaling.

## Contribution

A novel 3D hydrogel model was developed to study mechanoregulation of autophagy in periodontal ligament cells under realistic compression.

## Key findings

- Cells under compression showed increased autophagy markers like ATG7, Beclin1, and LC3-II/LC3-I within 4-8 hours.
- Pharmacological inhibition of AKT-mTOR enhanced autophagy, identifying it as a negative regulator.
- The hydrogel model mimics native matrix properties and enables quantitative studies of periodontal remodeling.

## Abstract

Mechanical loading is a central cue in periodontal tissues, where compression of the periodontal ligament guides remodeling and orthodontic tooth movement (OTM). However, most mechanobiology studies have used two-dimensional cultures with poorly defined loading, and the role of autophagy under realistic three-dimensional compression remains unclear. In this study, we constructed a three-dimensional static compression model by encapsulating human periodontal ligament cells in collagen–alginate–CaSO4 hydrogels, whose swelling, degradation, and viscoelasticity approximate those of native matrix. When exposed to a controlled static compressive stress, the cells exhibited an early autophagic response with increased ATG7, Beclin1, and LC3-II/LC3-I; accumulation of LC3-positive puncta; and reduced p62 expression between 4 and 8 h. Pharmacological modulation showed that activation of AKT-mTOR signaling suppressed this response, whereas its inhibition further augmented autophagy, identifying AKT-mTOR as a negative regulator of compression-induced autophagy. Together, these findings demonstrate that moderate static compression drives AKT-mTOR-dependent autophagy in periodontal ligament cells and establish a simple hydrogel platform for quantitative studies of periodontal remodeling.

## Linked entities

- **Genes:** ATG7 (autophagy related 7) [NCBI Gene 10533], BECN1 (beclin 1) [NCBI Gene 8678], Map1lc3a (microtubule-associated protein 1 light chain 3 alpha) [NCBI Gene 362245], Map1lc3a (microtubule-associated protein 1 light chain 3 alpha) [NCBI Gene 362245], GTF2H1 (general transcription factor IIH subunit 1) [NCBI Gene 2965], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207], MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475]
- **Chemicals:** alginate (PubChem CID 5102882), CaSO4 (PubChem CID 24497)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** NUP62 (nucleoporin 62) [NCBI Gene 23636] {aka IBSN, SNDI, p62}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, BECN1 (beclin 1) [NCBI Gene 8678] {aka ATG6, VPS30, beclin1}, ATG7 (autophagy related 7) [NCBI Gene 10533] {aka APG7-LIKE, APG7L, GSA7, SCAR31}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, MAP1LC3A (microtubule associated protein 1 light chain 3 alpha) [NCBI Gene 84557] {aka ATG8E, LC3, LC3A, MAP1ALC3, MAP1BLC3}
- **Chemicals:** CaSO4 (MESH:D002133), Alginate (MESH:D000464)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12841157/full.md

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Source: https://tomesphere.com/paper/PMC12841157