Elsevier

Microvascular Research

Volume 55, Issue 1, January 1998, Pages 65-76
Microvascular Research

Regular Article
Endothelial Cells from Diverse Tissues Exhibit Differences in Growth and Morphology

https://doi.org/10.1006/mvre.1997.2045Get rights and content
Under a Creative Commons license
open archive

Abstract

An increased recognition of the role of endothelial cells in disease and the development of methods for endothelial cell culture has led to an upsurge inin vitrostudies of endothelial cell function. However, the cells most often used for these studies do not reflect thein vivoheterogeneity of endothelial cells. To assess intrinsic differences between large and small vessel endothelial cells from different tissues, primary cultures of endothelial cells from capillaries (brain, lung, and adipose tissue) and a large vessel (aorta) of sheep were isolated, purified by fluorescence-activated cell sorting of acetylated low density lipoprotein (DiI-Ac-LDL) labeled cells, and characterized by phase contrast and ultrastructural morphology, expression of von Willebrand factor, and lack of expression of cytokeratin, smooth muscle actin, and glial fibrillary acidic protein (GFAP). Although all endothelial cells were cultured in the same media, only the brain microvascular endothelial cells demonstrated tight junctions by electron microscopy. Only the large vessel (aortic) endothelial cells contained Weibel–Palade bodies. Expression of von Willebrand factor decreased with passage of cells, but uptake of DiI-Ac-LDL was consistently positive regardless of culture conditions or passage number. These studies demonstrate that the unique ultrastructural characteristics of microvascular and macrovascular endothelial cells are intrinsic to the cells themselves and are not determined by differential culture conditions. This system allows the study of pathologic processes that affect endothelial cells of certain target organs selectively and should more accurately represent the response of tissue-specific endothelial cells in inflammatory processes.

Keywords

animal
sheep
endothelium
cell culture

Cited by (0)

J. CohenG. P. Wilkin