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膝关节骨关节炎:流行病学、发病机制和间充质干细胞:还有什么新进展?更新。

Knee Osteoarthritis: Epidemiology, Pathogenesis, and Mesenchymal Stem Cells: What Else Is New? An Update.

机构信息

IRCCS Istituto Ortopedico Galeazzi, 20161 Milan, Italy.

Residency Program in Orthopedics and Traumatology, University of Milan, 20141 Milan, Italy.

出版信息

Int J Mol Sci. 2023 Mar 29;24(7):6405. doi: 10.3390/ijms24076405.


DOI:10.3390/ijms24076405
PMID:37047377
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10094836/
Abstract

Osteoarthritis (OA) is a chronic disease and the most common orthopedic disorder. A vast majority of the social OA burden is related to hips and knees. The prevalence of knee OA varied across studies and such differences are reflected by the heterogeneity of data reported by studies conducted worldwide. A complete understanding of the pathogenetic mechanisms underlying this pathology is essential. The OA inflammatory process starts in the synovial membrane with the activation of the immune system, involving both humoral and cellular mediators. A crucial role in this process is played by the so-called "damage-associated molecular patterns" (DAMPs). Mesenchymal stem cells (MSCs) may be a promising option among all possible therapeutic options. However, many issues are still debated, such as the best cell source, their nature, and the right amount. Further studies are needed to clarify the remaining doubts. This review provides an overview of the most recent and relevant data on the molecular mechanism of cartilage damage in knee OA, including current therapeutic approaches in regenerative medicine.

摘要

骨关节炎(OA)是一种慢性疾病,也是最常见的骨科疾病。绝大多数的社会 OA 负担与髋关节和膝关节有关。膝关节 OA 的患病率在不同的研究中有所不同,这种差异反映了全球开展的研究报告的数据异质性。全面了解这种病理学的发病机制至关重要。OA 的炎症过程始于滑膜,免疫系统被激活,涉及体液和细胞介质。在这个过程中,所谓的“损伤相关分子模式”(DAMPs)起着关键作用。间充质干细胞(MSCs)可能是所有可能的治疗选择中最有前途的选择之一。然而,仍有许多问题存在争议,例如最佳细胞来源、其性质和合适的数量。需要进一步的研究来澄清剩余的疑问。本综述提供了关于膝骨关节炎软骨损伤的分子机制的最新和最相关的数据概述,包括再生医学中的当前治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccd4/10094836/039dc21a3baf/ijms-24-06405-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccd4/10094836/fd2a3f056ebb/ijms-24-06405-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccd4/10094836/039dc21a3baf/ijms-24-06405-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccd4/10094836/fd2a3f056ebb/ijms-24-06405-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccd4/10094836/039dc21a3baf/ijms-24-06405-g002.jpg

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Knee Osteoarthritis: Epidemiology, Pathogenesis, and Mesenchymal Stem Cells: What Else Is New? An Update.

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[2]
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[3]
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[7]
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[8]
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引用本文的文献

[1]
The Diagnostic Value of Musculoskeletal Ultrasound in Knee Osteoarthritis and Its Correlation with Pain Stratification.

J Musculoskelet Neuronal Interact. 2025-9-1

[2]
The Effects of Hyaluronic Acid on Gait Parameters in Patients with Knee Osteoarthritis: A Systematic Literature Review.

Medicina (Kaunas). 2025-8-20

[3]
[Predictors of Knee Replacement Following Meniscal Tear Arthroscopy: a 7-Year Risk Prediction Model].

Acta Chir Orthop Traumatol Cech. 2025-6

[4]
Postural correction training improves chronic pain, nerve function, and inflammation in knee osteoarthritis: A retrospective cohort study.

World J Orthop. 2025-8-18

[5]
Oral enzyme combination therapy reduces systemic inflammation, urinary CTXII and pain in knee osteoarthritis: a proof-of-mechanism, randomised, crossover, double-blind, placebo-controlled trial.

RMD Open. 2025-8-12

[6]
Comparative Outcomes Between Cruciate-Retaining and Posterior-Stabilized Prostheses in Total Knee Arthroplasty.

Cureus. 2025-7-7

[7]
Chinese Massage (Tuina) Attenuates Knee Osteoarthritis by Modulating Autophagy-Related Cytokines: A Multidisciplinary Methodological Investigation.

J Inflamm Res. 2025-8-2

[8]
Piezo1 induces mitochondrial autophagy dysfunction leading to cartilage injury in knee osteoarthritis.

Mol Med. 2025-8-2

[9]
Shengyu decoction ameliorates knee osteoarthritis by inhibiting endoplasmic reticulum stress via Piezo1 channels.

Front Pharmacol. 2025-7-14

[10]
Intra-articular Injections of Allogeneic Platelet-Rich Plasma from Responder Patients for the Treatment of Knee Osteoarthritis: A Pilot and Feasibility Clinical Trial.

Cartilage. 2025-7-29

本文引用的文献

[1]
Targeting macrophage polarization as a promising therapeutic strategy for the treatment of osteoarthritis.

Int Immunopharmacol. 2023-3

[2]
Comparative effectiveness of adipose-derived mesenchymal stromal cells in the management of knee osteoarthritis: A meta-analysis.

World J Orthop. 2023-1-18

[3]
Osteoarthritis: Pathogenesis, Animal Models, and New Regenerative Therapies.

J Clin Med. 2022-12-20

[4]
Intra-Articular Mesenchymal Stem Cell Injection for Knee Osteoarthritis: Mechanisms and Clinical Evidence.

Int J Mol Sci. 2022-12-21

[5]
CD14+ monocytes and soluble CD14 of synovial fluid are associated with osteoarthritis progression.

Arch Rheumatol. 2022-3-3

[6]
PRISMA-Compliant Meta-Analysis of Randomized Controlled Trials on Osteoarthritis of Knee Managed with Allogeneic vs Autologous MSCs: Efficacy and Safety Analysis.

Indian J Orthop. 2022-9-20

[7]
Molecular Mechanisms of Cartilage Repair and Their Possible Clinical Uses: A Review of Recent Developments.

Int J Mol Sci. 2022-11-17

[8]
Phenotypic and functional characterisation of synovial fluid-derived neutrophils in knee osteoarthritis and knee infection.

Osteoarthritis Cartilage. 2023-1

[9]
Soluble CCR2 gene therapy controls joint inflammation, cartilage damage, and the progression of osteoarthritis by targeting MCP-1 in a monosodium iodoacetate (MIA)-induced OA rat model.

J Transl Med. 2022-9-23

[10]
ALPK1 Accelerates the Pathogenesis of Osteoarthritis by Activating NLRP3 Signaling.

J Bone Miner Res. 2022-10

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