Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-j824f Total loading time: 0 Render date: 2024-11-08T08:10:40.110Z Has data issue: false hasContentIssue false

99 - Proteomic Mapping of Endothelium and Vascular Targeting in Vivo

from PART II - ENDOTHELIAL CELL AS INPUT-OUTPUT DEVICE

Published online by Cambridge University Press:  04 May 2010

Lucy A. Carver
Affiliation:
Sidney Kimmel Cancer Center, San Diego, California
Jan E. Schnitzer
Affiliation:
Sidney Kimmel Cancer Center, San Diego, California
William C. Aird
Affiliation:
Harvard University, Massachusetts
Get access

Summary

Endothelial cells (ECs) are highly adapted to meet the needs of local tissue and therefore acquire molecular and functional variation according to their location in the body. Although there is little question that the microenvironment of the tissue surrounding the blood vessels significantly influences EC phenotype, very little molecular information exists about vascular endothelium and the degree to which EC expression is modulated within different organs in vivo. Elucidating molecular expression and topography for ECs in multiple tissues constitutes the first step in a systems biology approach to gain a fundamental understanding of functional differences across organ systems and to frame future studies investigating how environmental inputs alter EC gene/protein expression and physiology. This information is vital also for tissue engineering, in which persists a critical lack of understanding of the properties of ECs in the context of normal tissues. By knowing EC expression in a given organ, researchers gain important topographical and functional knowledge, define the set of functional players in each endothelia, and gain key markers both to discover the factors leading to a particular phenotype and maybe to someday re-create the necessary tissue environment in culture. Finally, defining the endothelial proteome in healthy and diseased tissues may reveal further microen-vironmental modulation and may prove clinically useful by identifying new disease biomarkers and, perhaps more importantly, novel targets for site-directed delivery of functional and molecular imaging agents as well as nanomedicines, gene vectors, and drugs.

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
×