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Arteriosclerosis, Thrombosis, and Vascular Biology. 2004;24:691-696
Published online before print February 5, 2004, doi: 10.1161/01.ATV.0000120375.51196.73
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(Arteriosclerosis, Thrombosis, and Vascular Biology. 2004;24:691.)
© 2004 American Heart Association, Inc.


Vascular Biology

Embryonic Cell Lines with Endothelial Potential: An In Vitro System for Studying Endothelial Differentiation

Yijun Yin; Jianwen Que; Ming Teh; Wei Ping Cao; Reida Menshawe El Oakley; Sai-Kiang Lim

From the Department of Obstetrics and Gynaecology (Y.Y., S.-K.L.); Department of Surgery (J.Q., R.M.E.O.); Department of Pathology (M.T.); National University Medical Institute (P.C.), National University of Singapore; and Genome Institute of Singapore (S.-K.L.), Singapore. To better understand endothelial differentiation, an in vitro cellular system was established using embryonic cell lines empirically derived from mouse embryos. When plated on matrigel, the cells readily differentiated to form patent tubular structures that endocytosed acetylated LDL and expressed endothelial specific markers such as CD31, Flk-1, TIE2, and P-selectin.

Correspondence to Dr Sai-Kiang Lim, Genome Institute of Singapore, 60 Biopolis Street, Singapore 138672, Singapore. E-mail limsk{at}gis.a-star.edu.sg

Objective— Endothelial differentiation is a fundamental process in angiogenesis and vasculogenesis with implications in development, normal physiology, and pathology. To better understand this process, an in vitro cellular system that recapitulates endothelial differentiation and is amenable to experimental manipulations is required.

Methods and Results— Embryonic cell lines that differentiate exclusively into endothelial cells were derived from early mouse embryos using empirical but reproducible culture techniques without viral or chemical transformation. The cells were not pluripotent and expressed reduced levels of Oct 4 and Rex-1. They were non-tumorigenic with a population doubling time of {approx}15 hours. When plated on matrigel, they readily differentiated to form patent tubular structures with diameters of 30 to 150 µm. The differentiated cells endocytosed acetylated low-density lipoprotein (LDL) and began to express endothelial-specific markers such as CD34, CD31, Flk-1, TIE2, P-selectin, Sca-1, and thy-1. They also expressed genes essential for differentiation and maintenance of endothelial lineages, eg, Flk-1, vascular endothelial growth factor (VEGF), and angiopoietin-1. When transplanted into animal models, these cells incorporated into host vasculature.

Conclusions— These cell lines can undergo in vitro and in vivo endothelial differentiation that recapitulated known endothelial differentiation pathways. Therefore, they are ideal for establishing an in vitro cellular system to study endothelial differentiation.


Key Words: endothelial • progenitor cells • differentiation • embryonic cell line




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