Who drives the progress of osteoarthritis? – A descriptive study of synovium-meniscus crosstalk

Objective: The incidence of osteoarthritis (OA) increases with each passing year. The degeneration of the meniscus and synovium is considered the initial factor of knee osteoarthritis (KOA), but their synergistic mechanism has not been clarified. Methods: In this study, single-cell RNA sequencing (s...

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Main Authors: F Yu, TT Qi, J Weng, TB Wang, P Liu, YQ Chen, A Xiong, DL Wang, H Zeng
Format: Article
Language:English
Published: Forum Multimedia Publishing LLC 2024-10-01
Series:European Cells & Materials
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Online Access:https://www.ecmjournal.org/papers/vol048/vol048a06.php
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author F Yu
TT Qi
J Weng
TB Wang
P Liu
YQ Chen
A Xiong
DL Wang
H Zeng
author_facet F Yu
TT Qi
J Weng
TB Wang
P Liu
YQ Chen
A Xiong
DL Wang
H Zeng
author_sort F Yu
collection DOAJ
description Objective: The incidence of osteoarthritis (OA) increases with each passing year. The degeneration of the meniscus and synovium is considered the initial factor of knee osteoarthritis (KOA), but their synergistic mechanism has not been clarified. Methods: In this study, single-cell RNA sequencing (scRNA-seq) was employed to establish 16 normal or degenerated meniscus samples and 6 synovium samples based on the meniscus and synovium tissues of 16 patients. A cell atlas comprising 124,026 single cells in total was established (including 8 patients from the public database The Genome Sequence Archive for Human (GSA-Human) PRJCA008120). Results: Based on the exploration of the meniscus/synovium microenvironment homeostasis and the crosstalk between them during their degeneration, this study provided a comprehensive description of the involved cellular interactions. The cell types present in the meniscus and synovium were analyzed, and new fibroblast subtypes related to their degeneration were identified. Additionally, the interactions within pathways such as vascular endothelial growth factor (VEGF) and VISFATIN between the meniscus and synovium were studied, with a focus on various cell subtypes. The mechanisms involving vascular growth, immune cell infiltration, and common or distinct genes during the degeneration of synovium and meniscus tissues were also investigated. Conclusion: This study presented the largest cellular atlas of the synovium and meniscus in osteoarthritis (OA) to date, reflecting a detailed description of the cellular crosstalk during degeneration. The findings suggested that the synovium played a significant role in the intra-articular tissue crosstalk (synovium/meniscus), thereby contributing to the degeneration observed in OA.
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spelling doaj-art-a5e6d4167ee3484b927eb4fbceca98ad2025-08-20T02:36:53ZengForum Multimedia Publishing LLCEuropean Cells & Materials1473-22622024-10-01489311410.22203/eCM.v048a06Who drives the progress of osteoarthritis? – A descriptive study of synovium-meniscus crosstalkF YuTT QiJ WengTB WangP LiuYQ ChenA XiongDL WangH ZengObjective: The incidence of osteoarthritis (OA) increases with each passing year. The degeneration of the meniscus and synovium is considered the initial factor of knee osteoarthritis (KOA), but their synergistic mechanism has not been clarified. Methods: In this study, single-cell RNA sequencing (scRNA-seq) was employed to establish 16 normal or degenerated meniscus samples and 6 synovium samples based on the meniscus and synovium tissues of 16 patients. A cell atlas comprising 124,026 single cells in total was established (including 8 patients from the public database The Genome Sequence Archive for Human (GSA-Human) PRJCA008120). Results: Based on the exploration of the meniscus/synovium microenvironment homeostasis and the crosstalk between them during their degeneration, this study provided a comprehensive description of the involved cellular interactions. The cell types present in the meniscus and synovium were analyzed, and new fibroblast subtypes related to their degeneration were identified. Additionally, the interactions within pathways such as vascular endothelial growth factor (VEGF) and VISFATIN between the meniscus and synovium were studied, with a focus on various cell subtypes. The mechanisms involving vascular growth, immune cell infiltration, and common or distinct genes during the degeneration of synovium and meniscus tissues were also investigated. Conclusion: This study presented the largest cellular atlas of the synovium and meniscus in osteoarthritis (OA) to date, reflecting a detailed description of the cellular crosstalk during degeneration. The findings suggested that the synovium played a significant role in the intra-articular tissue crosstalk (synovium/meniscus), thereby contributing to the degeneration observed in OA.https://www.ecmjournal.org/papers/vol048/vol048a06.phposteoarthritiscrosstalksynoviummeniscussingle-cell rna sequencing
spellingShingle F Yu
TT Qi
J Weng
TB Wang
P Liu
YQ Chen
A Xiong
DL Wang
H Zeng
Who drives the progress of osteoarthritis? – A descriptive study of synovium-meniscus crosstalk
European Cells & Materials
osteoarthritis
crosstalk
synovium
meniscus
single-cell rna sequencing
title Who drives the progress of osteoarthritis? – A descriptive study of synovium-meniscus crosstalk
title_full Who drives the progress of osteoarthritis? – A descriptive study of synovium-meniscus crosstalk
title_fullStr Who drives the progress of osteoarthritis? – A descriptive study of synovium-meniscus crosstalk
title_full_unstemmed Who drives the progress of osteoarthritis? – A descriptive study of synovium-meniscus crosstalk
title_short Who drives the progress of osteoarthritis? – A descriptive study of synovium-meniscus crosstalk
title_sort who drives the progress of osteoarthritis a descriptive study of synovium meniscus crosstalk
topic osteoarthritis
crosstalk
synovium
meniscus
single-cell rna sequencing
url https://www.ecmjournal.org/papers/vol048/vol048a06.php
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