Abstract

Chronic liver disease (CLD) is a global health epidemic causing ∼2 million deaths annually worldwide. As the incidence of CLD is expected to rise over the next decade, understanding the cellular and molecular mediators of CLD is critical for developing novel therapeutics. Common characteristics of CLD include steatosis, inflammation, and cholesterol accumulation in the liver. While the lymphatic system in the liver has largely been overlooked, the liver lymphatics, as in other organs, are thought to play a critical role in maintaining normal hepatic function by assisting in the removal of protein, cholesterol, and immune infiltrate. Lymphatic growth, permeability, and/or hyperplasia in non-liver organs has been demonstrated to be caused by obesity or hypercholesterolemia in humans and animal models. While it is still unclear if changes in permeability occur in liver lymphatics, the lymphatics do expand in number and size in all disease etiologies tested. This is consistent with the lymphatic endothelial cells (LEC) upregulating proliferation specific genes, however, other transcriptional changes occur in liver LECs that are dependent on the inflammatory mediators that are specific to the disease etiology. Whether these changes induce lymphatic dysfunction or if they impact liver function has yet to be directly addressed. Here, we will review what is known about liver lymphatics in health and disease, what can be learned from recent work on the influence of obesity and hypercholesterolemia on the lymphatics in other organs, changes that occur in LECs in the liver during disease and outstanding questions in the field.

Highlights

  • The lymphatic system is comprised of highly permeable capillaries found within the tissue and are required to transport lymph which contains cellular proteins, lipoproteins and lymphocytes (Dixon et al, 2009; Lim et al, 2009; Platt et al, 2013; Hansen et al, 2015; Thomas et al, 2016; Schineis et al, 2019)

  • The capillaries drain into collecting lymphatic vessels (LV) surrounded by lymphatic muscle cells (LMC) that pump the lymph through highly specialized lymphatic valves (Chakraborty et al, 2015)

  • As we move forward into understanding differences in lymphatic endothelial cells (LEC) based on their tissue microenvironment we are likely to come across novel and specific pathways that could be targeted for disease therapeutics

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Summary

Emerging Roles for Lymphatics in Chronic Liver Disease

Reviewed by: Luis Villacorta, University of Michigan, United States Raghu P. Permeability, and/or hyperplasia in non-liver organs has been demonstrated to be caused by obesity or hypercholesterolemia in humans and animal models While it is still unclear if changes in permeability occur in liver lymphatics, the lymphatics do expand in number and size in all disease etiologies tested. This is consistent with the lymphatic endothelial cells (LEC) upregulating proliferation specific genes, other transcriptional changes occur in liver LECs that are dependent on the inflammatory mediators that are specific to the disease etiology.

INTRODUCTION
LIVER LYMPHATICS IN HEALTH
LIVER LYMPHATICS IN DISEASE
LIVER LYMPHATIC ENDOTHELIAL CELLS
Hepatocytes Cholangiocytes LSEC PEC LEC
OBESITY AND LYMPHATICS
VEGF AND CHYLOMICRON TRANSPORT
HYPERCHOLESTEROLEMIA AND LYMPHATICS
BYPASS OF FIRST PASS METABOLISM IN THE LIVER BY TARGETING LYMPHATICS
Findings
CONCLUSION AND FUTURE GOALS
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