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Curr Rheumatol Rev. 2023 Jun 5;19(3):246-259. doi: 10.2174/1573397119666230127144711.
2
Persistent popliteal lymphatic muscle cell coverage defects despite amelioration of arthritis and recovery of popliteal lymphatic vessel function in TNF-Tg mice following anti-TNF therapy.尽管 TNF-Tg 小鼠在接受抗 TNF 治疗后关节炎得到改善且腘窝淋巴管功能得到恢复,但仍然存在持续性的腘窝淋巴肌肉细胞覆盖缺陷。
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3
Single-cell transcriptomics of popliteal lymphatic vessels and peripheral veins reveals altered lymphatic muscle and immune cell populations in the TNF-Tg arthritis model.腘窝淋巴管和外周静脉的单细胞转录组学研究揭示了 TNF-Tg 关节炎模型中淋巴管肌和免疫细胞群体的改变。
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1
Lymphatic vessels: roles and potential therapeutic intervention in rheumatoid arthritis and osteoarthritis.淋巴管:类风湿关节炎和骨关节炎中的作用和潜在治疗干预。
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2
Distinct mast cell subpopulations within and around lymphatic vessels regulate lymph flow and progression of inflammatory-erosive arthritis in TNF-transgenic mice.在 TNF 转基因小鼠中,淋巴管内和周围的不同肥大细胞亚群调节淋巴液流动和炎症性侵蚀性关节炎的进展。
Front Immunol. 2023 Dec 14;14:1275871. doi: 10.3389/fimmu.2023.1275871. eCollection 2023.
3
Multi-omics analysis identifies IgG2b class-switching with ALCAM-CD6 co-stimulation in joint-draining lymph nodes during advanced inflammatory-erosive arthritis.多组学分析鉴定出在晚期炎症性侵蚀性关节炎时关节引流淋巴结中与 ALCAM-CD6 共刺激的 IgG2b 类别转换。
Front Immunol. 2023 Aug 25;14:1237498. doi: 10.3389/fimmu.2023.1237498. eCollection 2023.

本文引用的文献

1
Persistent popliteal lymphatic muscle cell coverage defects despite amelioration of arthritis and recovery of popliteal lymphatic vessel function in TNF-Tg mice following anti-TNF therapy.尽管 TNF-Tg 小鼠在接受抗 TNF 治疗后关节炎得到改善且腘窝淋巴管功能得到恢复,但仍然存在持续性的腘窝淋巴肌肉细胞覆盖缺陷。
Sci Rep. 2022 Jul 26;12(1):12751. doi: 10.1038/s41598-022-16884-y.
2
Lymphatic Collecting Vessel: New Perspectives on Mechanisms of Contractile Regulation and Potential Lymphatic Contractile Pathways to Target in Obesity and Metabolic Diseases.淋巴收集血管:收缩调节机制及肥胖和代谢性疾病中潜在可靶向的淋巴收缩途径的新观点
Front Pharmacol. 2022 Mar 9;13:848088. doi: 10.3389/fphar.2022.848088. eCollection 2022.
3
Lymphatic Valve Dysfunction in Western Diet-Fed Mice: New Insights Into Obesity-Induced Lymphedema.西方饮食喂养小鼠的淋巴管瓣膜功能障碍:对肥胖诱导性淋巴水肿的新见解。
Front Pharmacol. 2022 Mar 4;13:823266. doi: 10.3389/fphar.2022.823266. eCollection 2022.
4
Notoginsenoside R1 (NG-R1) Promoted Lymphatic Drainage Function to Ameliorating Rheumatoid Arthritis in TNF-Tg Mice by Suppressing NF-κB Signaling Pathway.三七皂苷R1(NG-R1)通过抑制NF-κB信号通路促进TNF-Tg小鼠的淋巴引流功能,从而改善类风湿性关节炎。
Front Pharmacol. 2022 Feb 24;12:730579. doi: 10.3389/fphar.2021.730579. eCollection 2021.
5
Single-cell transcriptomics of popliteal lymphatic vessels and peripheral veins reveals altered lymphatic muscle and immune cell populations in the TNF-Tg arthritis model.腘窝淋巴管和外周静脉的单细胞转录组学研究揭示了 TNF-Tg 关节炎模型中淋巴管肌和免疫细胞群体的改变。
Arthritis Res Ther. 2022 Mar 7;24(1):64. doi: 10.1186/s13075-022-02730-z.
6
Intra-articular injection of biologic anti-rheumatic drugs enhances local exposure to the joint-draining lymphatics.关节内注射生物类抗风湿药物可增强局部对关节引流淋巴管的暴露。
Eur J Pharm Biopharm. 2022 Apr;173:34-44. doi: 10.1016/j.ejpb.2022.02.014. Epub 2022 Feb 25.
7
Lymphangion-chip: a microphysiological system which supports co-culture and bidirectional signaling of lymphatic endothelial and muscle cells.淋巴管芯片:一种微生理系统,支持淋巴管内皮细胞和肌肉细胞的共培养和双向信号传递。
Lab Chip. 2021 Dec 21;22(1):121-135. doi: 10.1039/d1lc00720c.
8
Mesenteric lymphatic dysfunction promotes insulin resistance and represents a potential treatment target in obesity.肠系膜淋巴功能障碍会促进胰岛素抵抗,是肥胖症潜在的治疗靶点。
Nat Metab. 2021 Sep;3(9):1175-1188. doi: 10.1038/s42255-021-00457-w. Epub 2021 Sep 20.
9
Cross-tissue organization of the fibroblast lineage.成纤维细胞谱系的跨组织组织。
Nature. 2021 May;593(7860):575-579. doi: 10.1038/s41586-021-03549-5. Epub 2021 May 12.
10
Lymphatic endothelial-cell expressed ACKR3 is dispensable for postnatal lymphangiogenesis and lymphatic drainage function in mice.淋巴管内皮细胞表达的 ACKR3 对于小鼠出生后淋巴管生成和淋巴管引流功能是可有可无的。
PLoS One. 2021 Apr 15;16(4):e0249068. doi: 10.1371/journal.pone.0249068. eCollection 2021.

淋巴肌细胞之谜:它们从何而来,如何维持,能否再生?

The Enigmas of Lymphatic Muscle Cells: Where Do They Come From, How Are They Maintained, and Can They Regenerate?

机构信息

Center for Musculoskeletal Research, University of Rochester Medical Center, 601 Elmwood Ave, Box 665, Rochester, NY, 14642, USA.

Department of Pathology & Laboratory Medicine, University of Rochester Medical Center, Rochester, NY, USA.

出版信息

Curr Rheumatol Rev. 2023 Jun 5;19(3):246-259. doi: 10.2174/1573397119666230127144711.

DOI:10.2174/1573397119666230127144711
PMID:36705238
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10257750/
Abstract

Lymphatic muscle cell (LMC) contractility and coverage of collecting lymphatic vessels (CLVs) are integral to effective lymphatic drainage and tissue homeostasis. In fact, defects in lymphatic contractility have been identified in various conditions, including rheumatoid arthritis, inflammatory bowel disease, and obesity. However, the fundamental role of LMCs in these pathologic processes is limited, primarily due to the difficulty in directly investigating the enigmatic nature of this poorly characterized cell type. LMCs are a unique cell type that exhibit dual tonic and phasic contractility with hybrid structural features of both vascular smooth muscle cells (VSMCs) and cardiac myocytes. While advances have been made in recent years to better understand the biochemistry and function of LMCs, central questions regarding their origins, investiture into CLVs, and homeostasis remain unanswered. To summarize these discoveries, unexplained experimental results, and critical future directions, here we provide a focused review of current knowledge and open questions related to LMC progenitor cells, recruitment, maintenance, and regeneration. We also highlight the high-priority research goal of identifying LMC-specific genes towards genetic conditional- inducible in vivo gain and loss of function studies. While our interest in LMCs has been focused on understanding lymphatic dysfunction in an arthritic flare, these concepts are integral to the broader field of lymphatic biology, and have important potential for clinical translation through targeted therapeutics to control lymphatic contractility and drainage.

摘要

淋巴管肌细胞 (LMC) 的收缩性和收集淋巴管 (CLV) 的覆盖对于有效的淋巴引流和组织稳态至关重要。事实上,在各种情况下,包括类风湿性关节炎、炎症性肠病和肥胖症,已经发现了淋巴管收缩性缺陷。然而,LMC 在这些病理过程中的基本作用是有限的,主要是由于难以直接研究这种特征较差的神秘细胞类型。LMC 是一种独特的细胞类型,具有双重紧张性和阶段性收缩性,兼具血管平滑肌细胞 (VSMC) 和心肌细胞的混合结构特征。尽管近年来在更好地了解 LMC 的生物化学和功能方面取得了进展,但关于它们的起源、CLV 的投资以及稳态的核心问题仍未得到解答。为了总结这些发现、解释不明的实验结果和关键的未来方向,我们在这里提供了一篇关于 LMC 祖细胞、募集、维持和再生的当前知识和开放性问题的重点综述。我们还强调了确定 LMC 特异性基因的高优先级研究目标,以进行遗传条件诱导的体内获得和功能丧失研究。虽然我们对 LMC 的兴趣集中在理解关节炎发作中的淋巴功能障碍,但这些概念是淋巴生物学更广泛领域的重要组成部分,并且通过靶向治疗控制淋巴收缩性和引流具有重要的临床转化潜力。