Autophagy attenuates osteoarthritis in mice by inhibiting chondrocyte pyroptosis and improving subchondral bone remodeling

Osteoarthritis (OA) is an age-related degenerative disease characterized by cartilage degeneration and abnormal bone remodeling in the subchondral bone. Autophagy maintains cellular homeostasis by self-phagocytosis. However, the underlying mechanisms of autophagy on the pathological progression of O...

Full description

Bibliographic Details
Main Authors: Jiangbo Yan, Gangning Feng, Yong Yang, Dong Ding, Long Ma, Xin Zhao, Xiaolei Chen, Hui Wang, Zhirong Chen, Qunhua Jin
Format: Article
Language:English
Published: Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina 2023-01-01
Series:Biomolecules & Biomedicine
Subjects:
Online Access:https://www.bjbms.org/ojs/index.php/bjbms/article/view/7677
_version_ 1797261317369757696
author Jiangbo Yan
Gangning Feng
Yong Yang
Dong Ding
Long Ma
Xin Zhao
Xiaolei Chen
Hui Wang
Zhirong Chen
Qunhua Jin
author_facet Jiangbo Yan
Gangning Feng
Yong Yang
Dong Ding
Long Ma
Xin Zhao
Xiaolei Chen
Hui Wang
Zhirong Chen
Qunhua Jin
author_sort Jiangbo Yan
collection DOAJ
description Osteoarthritis (OA) is an age-related degenerative disease characterized by cartilage degeneration and abnormal bone remodeling in the subchondral bone. Autophagy maintains cellular homeostasis by self-phagocytosis. However, the underlying mechanisms of autophagy on the pathological progression of OA are still unknown. This study assessed the effects of autophagy on cartilage and subchondral bone in a mouse OA model. A mouse OA model was induced using destabilization of the medial meniscus (DMM) surgery. Assessment was performed by histomorphology, microcomputed tomography (micro-CT), immunohistochemical, immunofluorescent, and tartrate-resistant acid phosphatase (TRAP) staining. Our data revealed that autophagy can significantly delay the pathological progression of OA by increasing the thickness of hyaline cartilage and decreasing the thickness of calcified cartilage, increasing the subchondral bone volume fraction and bone mineralization density, and decreasing trabecular separation in the early stages of OA (2 weeks), whereas the opposite is true in the late stages of OA (8 weeks). Mechanistically, activation of autophagy in cartilage increased the expression of type II collagen (Col II), decreased the expression of matrix metalloproteinase 13 (MMP 13) and decreased the pyroptosis mediated by NOD-like receptor protein 3 (NLRP3) inflammasome by decreasing the expression of NLRP3, caspase-1, gasdermin D (GSDMD), and IL-1β. In the subchondral bone, activation of autophagy decreased the generation of mature osteoclasts at the early stages of OA (2 weeks) mainly by reducing the receptor activator for nuclear factor-κB ligand (RANKL)/osteoprotegerin (OPG) ratio, while it decreased osteoblastogenesis by reducing Runt-related transcription factor 2 (Runx2) expression significantly in the late stages of OA (8 weeks). In conclusion, autophagy may delay the pathological progression of OA in mice by inhibiting chondrocyte pyroptosis and improving subchondral bone remodeling.
first_indexed 2024-04-24T23:39:18Z
format Article
id doaj.art-bbe1da7899fd4d899b3069c57b36d08f
institution Directory Open Access Journal
issn 2831-0896
2831-090X
language English
last_indexed 2024-04-24T23:39:18Z
publishDate 2023-01-01
publisher Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina
record_format Article
series Biomolecules & Biomedicine
spelling doaj.art-bbe1da7899fd4d899b3069c57b36d08f2024-03-15T13:30:44ZengAssociation of Basic Medical Sciences of Federation of Bosnia and HerzegovinaBiomolecules & Biomedicine2831-08962831-090X2023-01-0123110.17305/bjbms.2022.7677Autophagy attenuates osteoarthritis in mice by inhibiting chondrocyte pyroptosis and improving subchondral bone remodelingJiangbo Yan0Gangning Feng1Yong Yang2Dong Ding3Long Ma4Xin Zhao5Xiaolei Chen6Hui Wang7Zhirong Chen8Qunhua Jin9Clinical College, Ningxia Medical University, Yinchuan, China; Orthopedics Ward 3, The General Hospital of Ningxia Medical University, Ningxia Medical University, Yinchuan, ChinaClinical College, Ningxia Medical University, Yinchuan, ChinaOrthopedics Ward 3, The General Hospital of Ningxia Medical University, Ningxia Medical University, Yinchuan, ChinaHand and Ankle Department, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, ChinaOrthopedics Ward 3, The General Hospital of Ningxia Medical University, Ningxia Medical University, Yinchuan, ChinaOrthopedics Ward 3, The General Hospital of Ningxia Medical University, Ningxia Medical University, Yinchuan, ChinaClinical College, Ningxia Medical University, Yinchuan, China; Orthopedics Ward 3, The General Hospital of Ningxia Medical University, Ningxia Medical University, Yinchuan, ChinaClinical College, Ningxia Medical University, Yinchuan, ChinaClinical College, Ningxia Medical University, Yinchuan, China; Orthopedics Ward 3, The General Hospital of Ningxia Medical University, Ningxia Medical University, Yinchuan, ChinaClinical College, Ningxia Medical University, Yinchuan, China; Orthopedics Ward 3, The General Hospital of Ningxia Medical University, Ningxia Medical University, Yinchuan, ChinaOsteoarthritis (OA) is an age-related degenerative disease characterized by cartilage degeneration and abnormal bone remodeling in the subchondral bone. Autophagy maintains cellular homeostasis by self-phagocytosis. However, the underlying mechanisms of autophagy on the pathological progression of OA are still unknown. This study assessed the effects of autophagy on cartilage and subchondral bone in a mouse OA model. A mouse OA model was induced using destabilization of the medial meniscus (DMM) surgery. Assessment was performed by histomorphology, microcomputed tomography (micro-CT), immunohistochemical, immunofluorescent, and tartrate-resistant acid phosphatase (TRAP) staining. Our data revealed that autophagy can significantly delay the pathological progression of OA by increasing the thickness of hyaline cartilage and decreasing the thickness of calcified cartilage, increasing the subchondral bone volume fraction and bone mineralization density, and decreasing trabecular separation in the early stages of OA (2 weeks), whereas the opposite is true in the late stages of OA (8 weeks). Mechanistically, activation of autophagy in cartilage increased the expression of type II collagen (Col II), decreased the expression of matrix metalloproteinase 13 (MMP 13) and decreased the pyroptosis mediated by NOD-like receptor protein 3 (NLRP3) inflammasome by decreasing the expression of NLRP3, caspase-1, gasdermin D (GSDMD), and IL-1β. In the subchondral bone, activation of autophagy decreased the generation of mature osteoclasts at the early stages of OA (2 weeks) mainly by reducing the receptor activator for nuclear factor-κB ligand (RANKL)/osteoprotegerin (OPG) ratio, while it decreased osteoblastogenesis by reducing Runt-related transcription factor 2 (Runx2) expression significantly in the late stages of OA (8 weeks). In conclusion, autophagy may delay the pathological progression of OA in mice by inhibiting chondrocyte pyroptosis and improving subchondral bone remodeling. https://www.bjbms.org/ojs/index.php/bjbms/article/view/7677Osteoarthritischondrocyteautophagypyroptosissubchondral bone
spellingShingle Jiangbo Yan
Gangning Feng
Yong Yang
Dong Ding
Long Ma
Xin Zhao
Xiaolei Chen
Hui Wang
Zhirong Chen
Qunhua Jin
Autophagy attenuates osteoarthritis in mice by inhibiting chondrocyte pyroptosis and improving subchondral bone remodeling
Biomolecules & Biomedicine
Osteoarthritis
chondrocyte
autophagy
pyroptosis
subchondral bone
title Autophagy attenuates osteoarthritis in mice by inhibiting chondrocyte pyroptosis and improving subchondral bone remodeling
title_full Autophagy attenuates osteoarthritis in mice by inhibiting chondrocyte pyroptosis and improving subchondral bone remodeling
title_fullStr Autophagy attenuates osteoarthritis in mice by inhibiting chondrocyte pyroptosis and improving subchondral bone remodeling
title_full_unstemmed Autophagy attenuates osteoarthritis in mice by inhibiting chondrocyte pyroptosis and improving subchondral bone remodeling
title_short Autophagy attenuates osteoarthritis in mice by inhibiting chondrocyte pyroptosis and improving subchondral bone remodeling
title_sort autophagy attenuates osteoarthritis in mice by inhibiting chondrocyte pyroptosis and improving subchondral bone remodeling
topic Osteoarthritis
chondrocyte
autophagy
pyroptosis
subchondral bone
url https://www.bjbms.org/ojs/index.php/bjbms/article/view/7677
work_keys_str_mv AT jiangboyan autophagyattenuatesosteoarthritisinmicebyinhibitingchondrocytepyroptosisandimprovingsubchondralboneremodeling
AT gangningfeng autophagyattenuatesosteoarthritisinmicebyinhibitingchondrocytepyroptosisandimprovingsubchondralboneremodeling
AT yongyang autophagyattenuatesosteoarthritisinmicebyinhibitingchondrocytepyroptosisandimprovingsubchondralboneremodeling
AT dongding autophagyattenuatesosteoarthritisinmicebyinhibitingchondrocytepyroptosisandimprovingsubchondralboneremodeling
AT longma autophagyattenuatesosteoarthritisinmicebyinhibitingchondrocytepyroptosisandimprovingsubchondralboneremodeling
AT xinzhao autophagyattenuatesosteoarthritisinmicebyinhibitingchondrocytepyroptosisandimprovingsubchondralboneremodeling
AT xiaoleichen autophagyattenuatesosteoarthritisinmicebyinhibitingchondrocytepyroptosisandimprovingsubchondralboneremodeling
AT huiwang autophagyattenuatesosteoarthritisinmicebyinhibitingchondrocytepyroptosisandimprovingsubchondralboneremodeling
AT zhirongchen autophagyattenuatesosteoarthritisinmicebyinhibitingchondrocytepyroptosisandimprovingsubchondralboneremodeling
AT qunhuajin autophagyattenuatesosteoarthritisinmicebyinhibitingchondrocytepyroptosisandimprovingsubchondralboneremodeling