Suppr超能文献

多种原发性淋巴水肿小鼠模型在淋巴静脉瓣膜发育中表现出明显缺陷。

Multiple mouse models of primary lymphedema exhibit distinct defects in lymphovenous valve development.

作者信息

Geng Xin, Cha Boksik, Mahamud Md Riaj, Lim Kim-Chew, Silasi-Mansat Robert, Uddin Mohammad K M, Miura Naoyuki, Xia Lijun, Simon Alexander M, Engel James Douglas, Chen Hong, Lupu Florea, Srinivasan R Sathish

机构信息

Cardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.

Department of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.

出版信息

Dev Biol. 2016 Jan 1;409(1):218-233. doi: 10.1016/j.ydbio.2015.10.022. Epub 2015 Nov 2.

Abstract

Lymph is returned to the blood circulation exclusively via four lymphovenous valves (LVVs). Despite their vital importance, the architecture and development of LVVs is poorly understood. We analyzed the formation of LVVs at the molecular and ultrastructural levels during mouse embryogenesis and identified three critical steps. First, LVV-forming endothelial cells (LVV-ECs) differentiate from PROX1(+) progenitors and delaminate from the luminal side of the veins. Second, LVV-ECs aggregate, align perpendicular to the direction of lymph flow and establish lympho-venous connections. Finally, LVVs mature with the recruitment of mural cells. LVV morphogenesis is disrupted in four different mouse models of primary lymphedema and the severity of LVV defects correlate with that of lymphedema. In summary, we have provided the first and the most comprehensive analysis of LVV development. Furthermore, our work suggests that aberrant LVVs contribute to lymphedema.

摘要

淋巴液仅通过四个淋巴静脉瓣(LVV)回流至血液循环。尽管它们至关重要,但LVV的结构和发育仍知之甚少。我们在小鼠胚胎发育过程中从分子和超微结构水平分析了LVV的形成,并确定了三个关键步骤。首先,形成LVV的内皮细胞(LVV-EC)从PROX1(+)祖细胞分化而来,并从静脉腔侧脱离。其次,LVV-EC聚集,垂直于淋巴流动方向排列并建立淋巴静脉连接。最后,LVV随着壁细胞的募集而成熟。在四种不同的原发性淋巴水肿小鼠模型中,LVV形态发生受到破坏,LVV缺陷的严重程度与淋巴水肿的严重程度相关。总之,我们提供了对LVV发育的首次也是最全面的分析。此外,我们的研究表明,异常的LVV会导致淋巴水肿。

相似文献

1
Multiple mouse models of primary lymphedema exhibit distinct defects in lymphovenous valve development.
Dev Biol. 2016 Jan 1;409(1):218-233. doi: 10.1016/j.ydbio.2015.10.022. Epub 2015 Nov 2.
2
Correlative Fluorescence and Scanning Electron Microscopy to Study Lymphovenous Valve Development.
Methods Mol Biol. 2018;1846:85-96. doi: 10.1007/978-1-4939-8712-2_6.
5
GATA2 regulates blood/lymph separation in a platelet-dependent and lymphovenous valve-independent manner.
Microcirculation. 2023 Apr;30(2-3):e12787. doi: 10.1111/micc.12787. Epub 2022 Oct 19.
6
Flow control in our vessels: vascular valves make sure there is no way back.
Cell Mol Life Sci. 2013 Mar;70(6):1055-66. doi: 10.1007/s00018-012-1110-6. Epub 2012 Aug 25.
8
GATA2 is required for lymphatic vessel valve development and maintenance.
J Clin Invest. 2015 Aug 3;125(8):2979-94. doi: 10.1172/JCI78888. Epub 2015 Jul 27.

引用本文的文献

2
S1PR1 regulates lymphatic valve development and tertiary lymphoid organ formation in the ileum.
J Exp Med. 2025 Sep 1;222(9). doi: 10.1084/jem.20241799. Epub 2025 Jun 24.
3
Meningeal lymphatic drainage: novel insights into central nervous system disease.
Signal Transduct Target Ther. 2025 May 5;10(1):142. doi: 10.1038/s41392-025-02177-z.
4
Lymphatic System Development and Function.
Curr Cardiol Rep. 2024 Nov;26(11):1209-1219. doi: 10.1007/s11886-024-02120-8. Epub 2024 Aug 22.
5
Connexin-45 is expressed in mouse lymphatic endothelium and required for lymphatic valve function.
JCI Insight. 2024 Jul 18;9(16):e169931. doi: 10.1172/jci.insight.169931.
6
Multiple cis-regulatory elements control prox1a expression in distinct lymphatic vascular beds.
Development. 2024 May 1;151(9). doi: 10.1242/dev.202525. Epub 2024 May 9.
7
The development of early human lymphatic vessels as characterized by lymphatic endothelial markers.
EMBO J. 2024 Mar;43(5):868-885. doi: 10.1038/s44318-024-00045-0. Epub 2024 Feb 14.
8
Hyperactive KRAS/MAPK signaling disrupts normal lymphatic vessel architecture and function.
Front Cell Dev Biol. 2023 Sep 25;11:1276333. doi: 10.3389/fcell.2023.1276333. eCollection 2023.
9
Temporospatial inhibition of Erk signaling is required for lymphatic valve formation.
Signal Transduct Target Ther. 2023 Sep 11;8(1):342. doi: 10.1038/s41392-023-01571-9.

本文引用的文献

1
GATA2 is required for lymphatic vessel valve development and maintenance.
J Clin Invest. 2015 Aug 3;125(8):2979-94. doi: 10.1172/JCI78888. Epub 2015 Jul 27.
3
Decoy receptor CXCR7 modulates adrenomedullin-mediated cardiac and lymphatic vascular development.
Dev Cell. 2014 Sep 8;30(5):528-40. doi: 10.1016/j.devcel.2014.07.012.
4
Molecular and cellular mechanisms of lymphatic vascular maturation.
Microvasc Res. 2014 Nov;96:16-22. doi: 10.1016/j.mvr.2014.06.002. Epub 2014 Jun 11.
6
Pkd1 regulates lymphatic vascular morphogenesis during development.
Cell Rep. 2014 May 8;7(3):623-33. doi: 10.1016/j.celrep.2014.03.063. Epub 2014 Apr 24.
7
Polycystin signaling is required for directed endothelial cell migration and lymphatic development.
Cell Rep. 2014 May 8;7(3):634-44. doi: 10.1016/j.celrep.2014.03.064. Epub 2014 Apr 24.
8
Control of retinoid levels by CYP26B1 is important for lymphatic vascular development in the mouse embryo.
Dev Biol. 2014 Feb 1;386(1):25-33. doi: 10.1016/j.ydbio.2013.12.008. Epub 2013 Dec 19.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验