The lymphatic system is a transport system that has important roles in fluid/macromolecule homeostasis, lipid absorption, metastasis and immune function. It accomplishes these roles via the generation of a regulated lymph circulation which is dependent upon valves and pumps to overcome the normal fluid pressure gradients. Lymphatic contractility plays crucial roles in the regulation and generation of lymph transport. Whereas our understanding of lymphatic contractility in humans is somewhat limited, a number of studies both in situ and in vitro have provided important insights into the presence and modulation of lymphatic contractility. These studies have clearly demonstrated that lymphatic vessels from a number of different human tissues possess both tonic and phasic changes in contractility. These changes in contractility are presumably involved in the generation and regulation of lymph flow. It has been shown that human lymphatic contractility can be influenced by a number of neural and humoral agents as a means to control lymph transport. However our understanding of the physical and chemical factors which regulate both the spontaneous pumping activity and the vessel tone are more limited. An understanding of thefactors which regulate human lymph transport could provide valuable information on human biology that could be of benefit to the treatment and prevention of diseases.
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Dev Cell
December 2024
Edwin L. Steele Laboratories, Department of Radiation Oncology, Massachusetts General Hospital Cancer Center, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA. Electronic address:
Lymphatic muscle cells (LMCs) within the wall of collecting lymphatic vessels exhibit tonic and autonomous phasic contractions, which drive active lymph transport to maintain tissue-fluid homeostasis and support immune surveillance. Damage to LMCs disrupts lymphatic function and is related to various diseases. Despite their importance, knowledge of the gene transcriptional signatures in LMCs and how they relate to lymphatic function in normal and disease contexts is largely missing.
View Article and Find Full Text PDFCirc Res
January 2025
Department of Pediatrics (J.Z., H.-C.Y., R.L.R., E.L.S., V.K.), Vanderbilt University Medical Center, Nashville, TN.
Background: Lymphatic collecting vessels in the kidney are critical in clearing interstitial fluid, macromolecules, and infiltrating immune cells. Dysfunction of the lymphatic vessels can disrupt this process and exacerbate injury-associated inflammation in many disease conditions. We previously found that sodium accumulates within the kidney interstitium during proteinuric kidney injury and elevated sodium environments stimulate isolevuglandin production in antigen-presenting cells, stimulating T cells, and modulating inflammatory responses.
View Article and Find Full Text PDFWorld J Gastroenterol
December 2024
Department of Colorectal and Anal Surgery (Clinical Center for Pelvic Floor Surgery), Clinical Center of Constipation and Pelvic Floor Disease of Wuhan, Hubei Key Laboratory of Intestinal and Colorectal Diseases, Clinical Center of Intestinal and Colorectal Diseases of Hubei Province, Quality Control Center of Colorectal and Anal Surgery of Health Commission of Hubei Province, Zhongnan Hospital of Wuhan University, Wuhan 430071, Hubei Province, China.
Background: Obstructed defecation syndrome (ODS) represents the most prevalent form of chronic constipation, affecting a diverse patient population, leading to numerous complications, and imposing a significant burden on healthcare resources. Most ODS patients have insufficient rectal propulsion, but the exact mechanism underlying the pathogenesis of ODS remains unclear.
Aim: To explore the molecular mechanism underlying the pathogenesis of ODS.
Hypertension
January 2025
Department of Pharmaceutical Sciences, College of Pharmacy (S.P., A.K.B., A.J.S.), University of Arkansas for Medical Sciences, Little Rock, AR.
Background: Hypertension increases the risk of lymphedema in patients with comorbidities, but whether hypertension directly compromises lymph vessel (LV) function and lymph flow is unclear. We compared the contractions of mesenteric LVs ex vivo and lymph flow in vivo between normotensive and Ang II (angiotensin II)-induced hypertensive rats and explored the ionic basis of contractile patterns. Key studies were recapitulated in spontaneously hypertensive rats and control Wistar-Kyoto rats.
View Article and Find Full Text PDFAnnu Rev Physiol
October 2024
2Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
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