Abstract
Simple SummaryLymphatic vessels are responsible for the drainage of liquids, solutes, and cells from interstitial spaces and serosal cavities. Their task is fundamental in order to avoid fluid accumulation leading to tissue swelling and edema. The lymphatic system does not possess a central pump, instead lymph is propelled against an overall hydraulic pressure gradient from interstitial spaces to central veins thanks to two pumping mechanisms, which rely on extrinsic forces or the intrinsic rhythmic contractility of lymphatic muscle cells embedded in vessel walls. This latter mechanism can very rapidly adapt to subtle changes in the microenvironment due to hydraulic pressure, lymph flow-induced wall shear stress, liquid osmolarity, and local tissue temperature. Thus, endothelial and lymphatic muscle cells possess mechanosensors that sense these stimuli and promote a change in contraction frequency and amplitude to modulate lymph flow accordingly. In this review, we will focus on the known physical parameters that can modulate lymph flow and on their putative cellular and molecular mechanisms of transduction.Lymphatic vessels drain and propel lymph by exploiting external forces that surrounding tissues exert upon vessel walls (extrinsic mechanism) and by using active, rhythmic contractions of lymphatic muscle cells embedded in the vessel wall of collecting lymphatics (intrinsic mechanism). The latter mechanism is the major source of the hydraulic pressure gradient where scant extrinsic forces are generated in the microenvironment surrounding lymphatic vessels. It is mainly involved in generating pressure gradients between the interstitial spaces and the vessel lumen and between adjacent lymphatic vessels segments. Intrinsic pumping can very rapidly adapt to ambient physical stimuli such as hydraulic pressure, lymph flow-derived shear stress, fluid osmolarity, and temperature. This adaptation induces a variable lymph flow, which can precisely follow the local tissue state in terms of fluid and solutes removal. Several cellular systems are known to be sensitive to osmolarity, temperature, stretch, and shear stress, and some of them have been found either in lymphatic endothelial cells or lymphatic muscle. In this review, we will focus on how known physical stimuli affect intrinsic contractility and thus lymph flow and describe the most likely cellular mechanisms that mediate this phenomenon.
Highlights
The lymphatic system drains fluid, macromolecules, and cells from the surrounding interstitium and from serosal cavities, contributing to tissue homeostasis and fluid balance [1,2]
We focus our attention on the known physical stimuli and their putative sensing mechanisms localized on the lymphatic vessel wall that can affect spontaneous contractility
Lymphatic endothelial cells (ECs) lining the inner lumen sense and respond to different stimuli acting on the vessel wall, such as the wall tension induced by transmural and/or intraluminal pressure and the inner wall shear stress
Summary
The lymphatic system drains fluid, macromolecules, and cells from the surrounding interstitium and from serosal cavities, contributing to tissue homeostasis and fluid balance [1,2]. Lymph formation formation and and propulsion propulsion depend depend upon upon two two different different mechanisms, mechanisms, named named “intrinsic “intrinsic and and extrinsic.” They both both affect affect local local pressure pressuregradients gradientsbetween betweeninterstitial interstitialspaces spacesand andvessel vessel lumen lumen and and between between adjacent lymphangions. Extrinsic and mechanisms [27], as the extrinsic respiratory mainlyboth sustain lymphatic intrinsic mechanisms cooperate [27],inasthe themedial extrinsic rhythmic respiratory mainly sustain propulsion in the central tendon and muscular region. In this movements regard, longitudinal rather lymphatic propulsion in the central tendon the medial muscular region. We focus our attention on the known physical stimuli and their putative sensing mechanisms localized on the lymphatic vessel wall that can affect spontaneous contractility
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