miR-1275 Delivered via Mesenchymal Stem Cell-Derived Extracellular Vesicles Regulates ER-Phagy Through AXIN2 in Nucleus Pulposus Cells

Intervertebral disc degeneration (IDD) is a major contributor to low back pain, a prevalent and debilitating condition. Nucleus pulposus (NP) cells are essential for maintaining disc homeostasis, and their dysfunction plays a crucial role in IDD development. This study aimed to explore the potential...

Full description

Saved in:
Bibliographic Details
Main Authors: Zhiwu Dong, Hailong Zhang, Wenwei Yang, Keliang Huang, Xin Zhang, Lianxiang Xing, Ying Zhang, Kewen Zhao
Format: Article
Language:English
Published: Wiley 2025-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/sci/5091529
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849467310901821440
author Zhiwu Dong
Hailong Zhang
Wenwei Yang
Keliang Huang
Xin Zhang
Lianxiang Xing
Ying Zhang
Kewen Zhao
author_facet Zhiwu Dong
Hailong Zhang
Wenwei Yang
Keliang Huang
Xin Zhang
Lianxiang Xing
Ying Zhang
Kewen Zhao
author_sort Zhiwu Dong
collection DOAJ
description Intervertebral disc degeneration (IDD) is a major contributor to low back pain, a prevalent and debilitating condition. Nucleus pulposus (NP) cells are essential for maintaining disc homeostasis, and their dysfunction plays a crucial role in IDD development. This study aimed to explore the potential role of miR-1275, delivered via mesenchymal stem cell-derived extracellular vesicles (MSCs-EVs), in IDD pathogenesis and to elucidate the underlying molecular mechanisms through in vitro investigations. Decreased miR-1275 expression and elevated endoplasmic reticulum (ER) stress were observed in degenerated human NP tissues compared to normal controls. An in vitro IDD model was established by treating NP cells (NPCs) with advanced glycation end products (AGEs). Subsequent experiments demonstrated that EVs from miR-1275-overexpressing MSCs reduced AGE-induced ER stress, extracellular matrix (ECM) degradation, and apoptosis in NPCs by enhancing ER-phagy. Bioinformatic analyses identified AXIN2 as a direct target of miR-1275. Remarkably, AXIN2 overexpression significantly attenuated the effects of miR-1275 on NPC proliferation, apoptosis, ER stress, and ER-phagy under AGE-induced conditions. Mechanistic studies validated AXIN2 as a target of miR-1275, with miR-1275 binding to the 3′ untranslated region of AXIN2 and regulating its expression. Collectively, our in vitro findings reveal that MSCs-EVs carrying miR-1275 can modulate ER stress and enhance ER-phagy in NPCs through the targeted downregulation of AXIN2, suggesting a potential molecular mechanism in IDD pathogenesis.
format Article
id doaj-art-c49d6d630e734e9a96dcd19fbf2c3721
institution Kabale University
issn 1687-9678
language English
publishDate 2025-01-01
publisher Wiley
record_format Article
series Stem Cells International
spelling doaj-art-c49d6d630e734e9a96dcd19fbf2c37212025-08-20T03:26:16ZengWileyStem Cells International1687-96782025-01-01202510.1155/sci/5091529miR-1275 Delivered via Mesenchymal Stem Cell-Derived Extracellular Vesicles Regulates ER-Phagy Through AXIN2 in Nucleus Pulposus CellsZhiwu Dong0Hailong Zhang1Wenwei Yang2Keliang Huang3Xin Zhang4Lianxiang Xing5Ying Zhang6Kewen Zhao7Department of Laboratory MedicineDepartment of OrthopedicsDepartment of Laboratory MedicineDepartment of Laboratory MedicineDepartment of Laboratory MedicineDepartment of Laboratory MedicineDepartment of Laboratory MedicineKey Laboratory of Cell Differentiation and Apoptosis of National Ministry of EducationIntervertebral disc degeneration (IDD) is a major contributor to low back pain, a prevalent and debilitating condition. Nucleus pulposus (NP) cells are essential for maintaining disc homeostasis, and their dysfunction plays a crucial role in IDD development. This study aimed to explore the potential role of miR-1275, delivered via mesenchymal stem cell-derived extracellular vesicles (MSCs-EVs), in IDD pathogenesis and to elucidate the underlying molecular mechanisms through in vitro investigations. Decreased miR-1275 expression and elevated endoplasmic reticulum (ER) stress were observed in degenerated human NP tissues compared to normal controls. An in vitro IDD model was established by treating NP cells (NPCs) with advanced glycation end products (AGEs). Subsequent experiments demonstrated that EVs from miR-1275-overexpressing MSCs reduced AGE-induced ER stress, extracellular matrix (ECM) degradation, and apoptosis in NPCs by enhancing ER-phagy. Bioinformatic analyses identified AXIN2 as a direct target of miR-1275. Remarkably, AXIN2 overexpression significantly attenuated the effects of miR-1275 on NPC proliferation, apoptosis, ER stress, and ER-phagy under AGE-induced conditions. Mechanistic studies validated AXIN2 as a target of miR-1275, with miR-1275 binding to the 3′ untranslated region of AXIN2 and regulating its expression. Collectively, our in vitro findings reveal that MSCs-EVs carrying miR-1275 can modulate ER stress and enhance ER-phagy in NPCs through the targeted downregulation of AXIN2, suggesting a potential molecular mechanism in IDD pathogenesis.http://dx.doi.org/10.1155/sci/5091529
spellingShingle Zhiwu Dong
Hailong Zhang
Wenwei Yang
Keliang Huang
Xin Zhang
Lianxiang Xing
Ying Zhang
Kewen Zhao
miR-1275 Delivered via Mesenchymal Stem Cell-Derived Extracellular Vesicles Regulates ER-Phagy Through AXIN2 in Nucleus Pulposus Cells
Stem Cells International
title miR-1275 Delivered via Mesenchymal Stem Cell-Derived Extracellular Vesicles Regulates ER-Phagy Through AXIN2 in Nucleus Pulposus Cells
title_full miR-1275 Delivered via Mesenchymal Stem Cell-Derived Extracellular Vesicles Regulates ER-Phagy Through AXIN2 in Nucleus Pulposus Cells
title_fullStr miR-1275 Delivered via Mesenchymal Stem Cell-Derived Extracellular Vesicles Regulates ER-Phagy Through AXIN2 in Nucleus Pulposus Cells
title_full_unstemmed miR-1275 Delivered via Mesenchymal Stem Cell-Derived Extracellular Vesicles Regulates ER-Phagy Through AXIN2 in Nucleus Pulposus Cells
title_short miR-1275 Delivered via Mesenchymal Stem Cell-Derived Extracellular Vesicles Regulates ER-Phagy Through AXIN2 in Nucleus Pulposus Cells
title_sort mir 1275 delivered via mesenchymal stem cell derived extracellular vesicles regulates er phagy through axin2 in nucleus pulposus cells
url http://dx.doi.org/10.1155/sci/5091529
work_keys_str_mv AT zhiwudong mir1275deliveredviamesenchymalstemcellderivedextracellularvesiclesregulateserphagythroughaxin2innucleuspulposuscells
AT hailongzhang mir1275deliveredviamesenchymalstemcellderivedextracellularvesiclesregulateserphagythroughaxin2innucleuspulposuscells
AT wenweiyang mir1275deliveredviamesenchymalstemcellderivedextracellularvesiclesregulateserphagythroughaxin2innucleuspulposuscells
AT kelianghuang mir1275deliveredviamesenchymalstemcellderivedextracellularvesiclesregulateserphagythroughaxin2innucleuspulposuscells
AT xinzhang mir1275deliveredviamesenchymalstemcellderivedextracellularvesiclesregulateserphagythroughaxin2innucleuspulposuscells
AT lianxiangxing mir1275deliveredviamesenchymalstemcellderivedextracellularvesiclesregulateserphagythroughaxin2innucleuspulposuscells
AT yingzhang mir1275deliveredviamesenchymalstemcellderivedextracellularvesiclesregulateserphagythroughaxin2innucleuspulposuscells
AT kewenzhao mir1275deliveredviamesenchymalstemcellderivedextracellularvesiclesregulateserphagythroughaxin2innucleuspulposuscells