Home LiteratureArticle Details
PMID: 18761022 Published · ppublish English Journal Article

Endosialin/TEM 1/CD248 is a pericyte marker of embryonic and tumor neovascularization.

Microvascular research ·Vol. 76 ·No. 3 ·2008-11-00 ·Pages 180-8

Bagley RG, Honma N, Weber W, Boutin P, Rouleau C, Shankara S, Kataoka S, Ishida I, Roberts BL, Teicher BA

Abstract

The formation of functional, mature blood vessels depends on the interaction between endothelial cells and pericytes. Commonality exists in the processes involved in vasculature development between tissues whether healthy or diseased. Endosialin/TEM 1 is a cell membrane protein that is expressed in blood vessels during embryogenesis and tumorigenesis but not in normal mature vessels. Antibodies developed to human endosialin were used to investigate endosialin expression and function in human prenatal brain pericytes and pericytes residing in tumors. Anti-endosialin was capable of preventing pericyte tube formation in culture and inhibited migration. Brain pericytes in culture had higher levels of endosialin/TEM 1 than TEMs-2, -3, -4, -5, -7, and -8. Immunocytochemistry revealed that endosialin was present in the cytoplasmic body and in the elongated extensions essential to pericyte function. Transgenic mice engineered to express human endosialin bred on an immunocompromised background allowed the growth of human tumor xenografts. In human colon carcinoma Colo205 and HT29 xenografts grown in human endosialin-transgenic mice, endosialin expression was largely confined to NG2-expressing perivascular cells and not CD31-positive endothelial cells. Similar methods applied to human ovarian and colon tumors confirmed endosialin expression by pericytes. The data indicate that endosialin is strongly expressed by pericytes during periods of active angiogenesis during embryonic and tumor development. Anti-endosialin antibodies may have value in identifying vasculature in malignant tissues. With the appropriate agent, targeting endosialin may interfere with blood vessel growth during tumor development.

MeSH Terms
Animals Antigens, CD/genetics,metabolism Antigens, Neoplasm/genetics,metabolism Base Sequence Cell Line, Tumor Cells, Cultured DNA Primers/genetics Embryonic Development Female Gene Expression Humans Male Mice Mice, Inbred C57BL Mice, SCID Mice, Transgenic Neoplasms, Experimental/blood supply,metabolism Neovascularization, Pathologic Neovascularization, Physiologic Pericytes/cytology,metabolism Recombinant Proteins/genetics,metabolism Transplantation, Heterologous
Chemicals
Antigens, CD Antigens, Neoplasm CD248 protein, human DNA Primers Recombinant Proteins
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Bagley Rebecca G
Genzyme Corporation, 49 New York Avenue Framingham, MA 01701-9322, USA. [email protected]
Honma Nakayuki
Weber William
Boutin Paula
Rouleau Cecile
Shankara Srinivas
Kataoka Shiro
Ishida Isao
Roberts Bruce L
Teicher Beverly A
Article Info
Journal
Microvascular research
Abbr.
Microvasc Res
ISSN
1095-9319
Published
2008-11-00
Epub
2008-00-08
Pages
180-8
Language
English
Region
United States
NLM ID
0165035
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]