Novel mouse endothelial cell surface marker is suppressed during differentiation of the blood brain barrier
Article first published online: 3 FEB 2005
Copyright © 1995 Wiley-Liss, Inc.
Volume 202, Issue 4, pages 325–332, April 1995
How to Cite
Hallmann, R., Mayer, D. N., Berg, E. L., Broermann, R. and Butcher, E. C. (1995), Novel mouse endothelial cell surface marker is suppressed during differentiation of the blood brain barrier. Dev. Dyn., 202: 325–332. doi: 10.1002/aja.1002020402
- Issue published online: 3 FEB 2005
- Article first published online: 3 FEB 2005
- Manuscript Accepted: 7 NOV 1994
- Manuscript Received: 19 SEP 1994
- Blood brain barrier;
- Differentiation marker
Few markers specific for mouse endothelium exist. We describe here one such marker, MECA-32, a monoclonal antibody which shows high specificity for mouse endothelium in both embryonic and mature tissues. The MECA-32 antigen has a Mr of 50−55 − 103 under reducing conditions and Mr of 100−120 − 103 under nonreducing conditions. It is expressed on most endothelial cells in the embryonic and in the adult mouse, with the exception of the brain, skeletal, and cardiac muscle, where it has a more restricted distribution. In skeletal and cardiac muscle only small arterioles and venules express the MECA-32 antigen, while in the brain its expression is negatively correlated with the differentiation of the vasculature to form the blood brain barrier. Interestingly, during embryonic development the antigen occurs on the brain vasculature up to day 16 of gestation (E16), whereupon it disappears. The embryonic brain is an avascular organ anlage which is vascularized by ingrowth of external blood vessels. Differentiation of the vasculature to form the blood brain barrier occurs at approximately E16 in the mouse. This differentiation correlates with the downregulation of MECA-32 antigen expression. Between E12 and E16 MECA-32 detects most endothelial cell surfaces of the blood vessels in the brain. No MECA-32 antigen is found in the brain at E17 or any later stage of development with the exception of the vasculature of the circumventricular organs. The results suggest that MECA-32 antigen expression is temporally and spatially correlated with the development of the blood brain barrier. © 1995 Wiley-Liss, Inc.