Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-j824f Total loading time: 0 Render date: 2024-11-08T07:20:25.578Z Has data issue: false hasContentIssue false

66 - Interactions between Hepatocytes and Liver Sinusoidal Endothelial Cells

from PART II - ENDOTHELIAL CELL AS INPUT-OUTPUT DEVICE

Published online by Cambridge University Press:  04 May 2010

David Semela
Affiliation:
Mayo Clinic, Rochester, Minnesota
Vijay Shah
Affiliation:
Mayo Clinic, Rochester, Minnesota
William C. Aird
Affiliation:
Harvard University, Massachusetts
Get access

Summary

The liver is the largest organ in the body and, in humans, weighs between 1,400 and 1,600 g (2.5% of total body weight). It receives 25% of the total cardiac output, which arrives via the hepatic artery (one-third of hepatic blood flow) and the portal vein (two-thirds of hepatic blood flow). Blood flows through liver sinusoids, a unique microvasculature that consists of plates of liver sinusoidal endothelial cells (LSECs) between plates of hepatocytes, before coming in contact with the liver parenchyma. LSECs account for 20% of total liver cells (an estimated 1 × 108 cells) whereas hepatocytes represent the majority of liver cells (estimated 60% or 3 × 108 cells). The remaining cell populations are (a) hepatic stellate cells (HSCs) (5%–8%), which are liver-specific pericytes; (b) biliary epithelial cells, also known as cholangiocytes, which line the bile ducts; and (c) macrophages called Kupffer cells. LSECs are unique in comparison to other organs in that they possess multiple fenestrae (pores) arranged in sieve plates (Figure 66.1) and lack an organized basement membrane. LSECs lie in close proximity to hepatocytes, and the interaction of these two cell types has been the subject of intense study. Cellular cross-talk between LSECs and hepatocytes plays an important role in homeostasis and physiologic processes such as liver organogenesis and liver regeneration. Moreover, abnormalities in intercellular communication underlie virtually every disease of the liver, including acute and chronic inflammatory liver disease, liver fibrosis, and hepatocarcinogenesis. Of these physiological and pathological states, liver regeneration is the most studied and best understood. Thus, this chapter focuses primarily on the latter model as a means to explore the biology of hepatocyte–endothelial cell (EC) interactions.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2007

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×