|
Human Brain Microvascular Endothelial
Cells
(HBMEC)
|
| Catalog Number: 1000 |
|
Cell Specification
The brain microvascular endothelial cells are the major
element of the blood-brain barrier and comprises the primary limitation
to passage of substances, both soluble and cellular, from the blood
into the brain. Brain microvascular endothelial cells utilize unique
features that distinguish themselves from those of peripheral endothelial
cells such as 1) numerous intercellular'tight junctions' that display
high transendothelial electrical resistance and retard paracellular
flux [1]; 2) absence of fenestrae and a reduced level of fluid-phase
endocytosis [2] and 3) asymmetrically-localized enzymes and carrier-mediated
transport systems that engender a truly 'polarized' phenotype [3].
Like peripheral endothelial cells, however, brain microvacular endothelial
cells express cell adhesion molecules on their surface that regulate
the extravasation of leukocytes into the brain. In view of the organ
specificity of microvascular endothelial cells, endothelial cells
should be derived from the tissue involved in the diseases one wishes
to study.
HBMEC from ScienCell Research Laboratories are isolated from human
brain tissue. HBMEC are cryopreserved immediately after purification
and delivered frozen. Each vial contains >5 x 105
cells in 1 ml volume. HBMEC are characterized by immunofluorescent
method with antibodies to vWF/Factor VIII and CD31 (P-CAM), by uptake
of DiI-Ac-LDL and by the formation of microtublar structure in
vitro. HBMEC are negative for HIV-1, HBV, HCV, mycoplasma, bacteria,
yeast and fungi. HBMEC are guaranteed to further expand in the conditions
specified by ScienCell Research Laboratories.
Recommended Medium
It is recommended to use Endothelial Cell Medium (ECM,
Cat. No. 1001) for the culturing of HBMEC in vitro.
Product Use
HBMEC are for research use only. They are not approved
for human or animal use, or for application in in vitro diagnostic
procedures.
Storage
Transfer cells directly and immediately from dry ice to liquid nitrogen
upon receiving and keep the cells in liquid nitrogen until cell
culture is needed for experiments.
Shipping
Dry ice.
Reference
[1] Crone, C. and Oleson, S. P. (1992) Electrical resistance of
brain microvessel endothelium. Brain Res. 241: 49-55.
[2] Reese, T. S. and Karnovsky, M. J. (1967) Fine structural localization
of blood-brain barrier to exogenous peroxidase. J. Cell Biol. 34:9-14.
[3] Vorbrodt, A. W. (1988) Ultrastructural cytochemistry of blood-brain
barrier endothelia. Prog. Histochem. Cytochem. 18(3):1-96. |