Abouelkheir Gabriella R, Upchurch Bradley D, Rutkowski Joseph M
1 Division of Lymphatic Biology, Department of Medical Physiology, Texas A&M College of Medicine, College Station, TX 77843, USA.
Exp Biol Med (Maywood). 2017 Apr;242(8):884-895. doi: 10.1177/1535370217697385. Epub 2017 Mar 7.
Lymphangiogenesis is a recognized hallmark of inflammatory processes in tissues and organs as diverse as the skin, heart, bowel, and airways. In clinical and animal models wherein the signaling processes of lymphangiogenesis are manipulated, most studies demonstrate that an expanded lymphatic vasculature is necessary for the resolution of inflammation. The fundamental roles that lymphatics play in fluid clearance and immune cell trafficking from the periphery make these results seemingly obvious as a mechanism of alleviating locally inflamed environments: the lymphatics are simply providing a drain. Depending on the tissue site, lymphangiogenic mechanism, or induction timeframe, however, evidence shows that inflammation-associated lymphangiogenesis (IAL) may worsen the pathology. Recent studies have identified lymphatic endothelial cells themselves to be local regulators of immune cell activity and its consequential phenotypes - a more active role in inflammation regulation than previously thought. Indeed, results focusing on the immunocentric roles of peripheral lymphatic function have revealed that the basic drainage task of lymphatic vessels is a complex balance of locally processed and transported antigens as well as interstitial cytokine and immune cell signaling: an interplay that likely defines the function of IAL. This review will summarize the latest findings on how IAL impacts a series of disease states in various tissues in both preclinical models and clinical studies. This discussion will serve to highlight some emerging areas of lymphatic research in an attempt to answer the question relevant to an array of scientists and clinicians of whether IAL helps to fuel or extinguish inflammation. Impact statement Inflammatory progression is present in acute and chronic tissue pathologies throughout the body. Lymphatic vessels play physiological roles relevant to all medical fields as important regulators of fluid balance, immune cell trafficking, and immune identity. Lymphangiogenesis is often concurrent with inflammation and can potentially aide or worsen disease progression. How new lymphatic vessels impact inflammation and by which mechanism is an important consideration in current and future clinical therapies targeting inflammation and/or vasculogenesis. This review identifies, across a range of tissue-specific pathologies, the current understanding of inflammation-associated lymphangiogenesis in the progression or resolution of inflammation.
淋巴管生成是组织和器官炎症过程的一个公认标志,这些组织和器官包括皮肤、心脏、肠道和气道等多种类型。在临床和动物模型中,淋巴管生成的信号传导过程受到操控,大多数研究表明,扩张的淋巴管系统对于炎症的消退是必要的。淋巴管在液体清除和外周免疫细胞运输中所起的基本作用,使得这些结果作为减轻局部炎症环境的一种机制似乎显而易见:淋巴管仅仅是提供了一个引流途径。然而,根据组织部位、淋巴管生成机制或诱导时间框架的不同,有证据表明炎症相关的淋巴管生成(IAL)可能会使病理状况恶化。最近的研究已经确定淋巴管内皮细胞本身是免疫细胞活性及其相关表型的局部调节因子——在炎症调节中发挥着比以前认为的更积极的作用。事实上,关注外周淋巴功能免疫中心作用的研究结果表明,淋巴管的基本引流任务是局部加工和运输抗原以及间质细胞因子和免疫细胞信号的复杂平衡:这种相互作用可能决定了IAL的功能。这篇综述将总结IAL如何影响临床前模型和临床研究中各种组织的一系列疾病状态的最新发现。本次讨论将有助于突出淋巴管研究中一些新出现的领域,试图回答一系列科学家和临床医生都关心的问题,即IAL是有助于加剧还是消除炎症。影响声明炎症进展存在于全身的急性和慢性组织病理学中。淋巴管作为液体平衡、免疫细胞运输和免疫特性的重要调节因子,在所有医学领域都发挥着重要的生理作用。淋巴管生成通常与炎症同时发生,并且可能有助于或恶化疾病进展。新的淋巴管如何影响炎症以及通过何种机制,是当前和未来针对炎症和/或血管生成的临床治疗中一个重要的考虑因素。这篇综述在一系列组织特异性病理学中,确定了目前对炎症相关淋巴管生成在炎症进展或消退中的理解。