ASIC3 roles in mechanosensitive elongation of nucleus pulposus cells.

3D culture ASIC3 Mechano-signaling Nucleus pulposus

Journal

Journal of biomechanics
ISSN: 1873-2380
Titre abrégé: J Biomech
Pays: United States
ID NLM: 0157375

Informations de publication

Date de publication:
10 Jan 2024
Historique:
received: 08 03 2023
revised: 14 12 2023
accepted: 04 01 2024
medline: 14 1 2024
pubmed: 14 1 2024
entrez: 13 1 2024
Statut: aheadofprint

Résumé

Morphological changes of the nucleus pulposus (NP) cells occur concomitantly as part of the intervertebral disc (IVD) degeneration and excessive mechanical loading has been speculated as a significant key factor for contributing to such morphological changes. Therefore, we hypothesize that stress exerted on NP cells can cause a deformity of nucleus in response. The changes of cell morphology is observed in degenerative nucleus pulposus. One of the reasons for degeneration of NP is due to overloading of NP especially in the obese population. So the nucleus deformity caused by stress/force is of our study interest. To delineate the effects and role of mechanical stress, we developed a 3D assay using hydrogel cultures with a circular hole generated with needle indentation to simulate a local stress concentration along the edge of the hole. A stressed zone, encompassing 100 μm of range from the circular edge, is defined based on stress concentration calculation to enable quantitative analysis against the control zone. Our results demonstrated that the circular hole produces stress-induced morphological changes in NP cells. The tangential elongation of NP cells and their nucleus shape changes in the stressed zone are significantly increased compared to the non-stressed control zone. It is proposed that the cell elongation is a direct response to elevated stress within the stressed zone. Subsequently we found the stress induced morphological changes of the NP cells can be significantly reduced by inhibiting ASIC3. This suggests ASIC3 plays an important role of play in mechano-signaling of NP cells.

Identifiants

pubmed: 38217980
pii: S0021-9290(24)00015-0
doi: 10.1016/j.jbiomech.2024.111938
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

111938

Informations de copyright

Copyright © 2024 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Jaw-Lin Wang reports financial support was provided by Ministry of Science and Technology, Taiwan. Jaw-Lin Wang reports financial support was provided by National Health Research Institute, Taiwan. Jaw-Lin Wang reports a relationship with Ministry of Science and Technology, Taiwan that includes: funding grants.

Auteurs

Jormay Lim (J)

Department of Biomedical Engineering, College of Medicine and College of Engineering, Nation Taiwan University, Taipei, Taiwan.

Shao-Shiang Huang (SS)

Department of Biomedical Engineering, College of Medicine and College of Engineering, Nation Taiwan University, Taipei, Taiwan.

Mohammad Nikkhoo (M)

Graduate Institute of Rehabilitation Science, College of Medicine, Chang Gung University, Taoyuan, Taiwan.

Wei-Ting Tai (WT)

Department of Biomedical Engineering, College of Medicine and College of Engineering, Nation Taiwan University, Taipei, Taiwan.

Ya-Cherng Chu (YC)

Department of Biomedical Engineering, College of Medicine and College of Engineering, Nation Taiwan University, Taipei, Taiwan; Center of Medical Devices, National Taiwan University, Taipei, Taiwan.

Andy Chien (A)

Department of Biomedical Engineering, College of Medicine and College of Engineering, Nation Taiwan University, Taipei, Taiwan.

Jaw-Lin Wang (JL)

Department of Biomedical Engineering, College of Medicine and College of Engineering, Nation Taiwan University, Taipei, Taiwan; Center of Medical Devices, National Taiwan University, Taipei, Taiwan. Electronic address: jlwang@ntu.edu.tw.

Classifications MeSH