Gashev Anatoliy A, Zawieja David C
Department of Systems Biology and Translational Medicine, Cardiovascular Research Institute Division of Lymphatic Biology, College of Medicine, Texas A&M Health Science Center, 702 SW H.K. Dodgen Loop, Temple, TX 76504, USA.
Pathophysiology. 2010 Sep;17(4):277-87. doi: 10.1016/j.pathophys.2009.09.002. Epub 2010 Mar 11.
To accomplish its normal roles in body fluid regulation/macromolecular homeostasis, immune function, and lipid absorption; the lymphatic system must transport lymph from the interstitial spaces, into and through the lymphatics, through the lymphatic compartment of the nodes, back into the nodal efferent lymphatics and eventually empty into the great veins. The usual net pressure gradients along this path do not normally favor the passive movement of lymph. Thus, lymph transport requires the input of energy to the lymph to propel it along this path. To do this, the lymphatic system uses a series of pumps to generate lymph flow. Thus to regulate lymph transport, both lymphatic pumping and resistance must be controlled. This review focuses on the regulation of the intrinsic lymph pump by hydrodynamic factors and how these regulatory processes are altered with age. Intrinsic lymph pumping is generated via the rapid/phasic contractions of lymphatic muscle, which are modulated by local physical factors (pressure/stretch and flow/shear). Increased lymph pressure/stretch will generally activate the intrinsic lymph pump up to a point, beyond which the lymph pump will begin to fail. The effect of increased lymph flow/shear is somewhat more complex, in that it can either activate or inhibit the intrinsic lymph pump, depending on the pattern and magnitude of the flow. The pattern and strength of the hydrodynamic regulation of the lymph transport is different in various parts of the lymphatic tree under normal conditions, depending upon the local hydrodynamic conditions. In addition, various pathophysiological processes can affect lymph transport. We have begun to evaluate the influence of the aging process on lymphatic transport characteristics in the rat thoracic duct. The pressure/stretch-dependent activation of intrinsic pumping is significantly impaired in aged rat thoracic duct (TD) and the flow/shear-dependent regulatory mechanisms are essentially completely lacking. The loss of shear-dependent modulation of lymphatic transport appears to be related to a loss of normal eNOS expression and a large rise in iNOS expression in these vessels. Therefore, aging of the lymph transport system significantly impairs its ability to transport lymph. We believe this will alter normal fluid balance as well as negatively impact immune function in the aged animals. Further studies are needed to detail the mechanisms that control and alter lymphatic transport during normal and aged conditions.
为了在体液调节/大分子稳态、免疫功能和脂质吸收中发挥其正常作用,淋巴系统必须将淋巴从组织间隙输送到淋巴管内并通过淋巴管,经过淋巴结的淋巴腔,再回到淋巴结的输出淋巴管,最终排入大静脉。沿着这条路径的通常净压力梯度通常并不利于淋巴的被动移动。因此,淋巴运输需要向淋巴输入能量以推动其沿此路径流动。为此,淋巴系统使用一系列泵来产生淋巴流动。因此,要调节淋巴运输,必须同时控制淋巴泵浦和阻力。本综述重点关注流体动力学因素对内在淋巴泵的调节以及这些调节过程如何随年龄变化。内在淋巴泵浦是通过淋巴肌的快速/阶段性收缩产生的,这些收缩由局部物理因素(压力/拉伸和流量/剪切力)调节。淋巴压力/拉伸增加通常会在一定程度上激活内在淋巴泵浦,超过这一点,淋巴泵浦就会开始失效。淋巴流量/剪切力增加的影响则更为复杂,因为它可以根据流量的模式和大小激活或抑制内在淋巴泵浦。在正常情况下,根据局部流体动力学条件,淋巴运输的流体动力学调节模式和强度在淋巴树的不同部位有所不同。此外,各种病理生理过程会影响淋巴运输。我们已经开始评估衰老过程对大鼠胸导管淋巴运输特征的影响。在老年大鼠胸导管(TD)中,压力/拉伸依赖性的内在泵浦激活明显受损,并且流量/剪切力依赖性调节机制基本完全缺失。淋巴运输的剪切力依赖性调节丧失似乎与这些血管中正常内皮型一氧化氮合酶(eNOS)表达的丧失以及诱导型一氧化氮合酶(iNOS)表达的大幅增加有关。因此,淋巴运输系统的衰老会显著损害其运输淋巴的能力。我们认为这将改变正常的体液平衡,并对老年动物的免疫功能产生负面影响。需要进一步研究来详细阐明在正常和衰老条件下控制和改变淋巴运输的机制。