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Human Intestinal Microvascular Endothelial
Cells
(HIMEC)
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| Catalog Number: 2900 |
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Cell Specification
Endothelial cells lining the microvasculature are known to play
a critical "gatekeeper" role in the inflammatory process through
their ability to recruit circulating immune cells into tissues and
foci of inflammation. Endothelial activation in response to cytokines
and bacterial products results in cell adhesion molecule expression
and chemokine production, which mediate increased binding and transmigration
of leukocytes across the vascular wall. Studies show that intestinal
microvascular endothelial cells (IMEC) exhibit a strong immune response
to LPS challenge and play a critical regulatory role in gut inflammation
[1]. Pharmacological inhibition of NOS in activated HIMEC resulted
in a significant increase in leukocytes binding [2]. Gene expression
profile study reveals that intestinal endothelial cells express
biotinidase, which is involved in biotin recycling [3]. The in
vitro culture of HIMEC enabled scientists to perform systematic
analyses of the cytokine profiles with regard to mRNA expression
and protein secretion, and to compare such data with cytokine profiles
concomitantly displayed by other endothelial cells.
HIMEC from ScienCell Research Laboratories are isolated from human
intestinal tissue. HIMEC are cryopreserved at passage one and delivered
frozen. Each vial contains >5 x 105 cells in 1 ml volume. HIMEC
are characterized by immunofluorescent method with antibodies to
vWF/Factor VIII and CD31 (P-CAM) and by uptake of DiI-Ac-LDL. HIMEC
are negative for HIV-1, HBV, HCV, mycoplasma, bacteria, yeast and
fungi. HIMEC are guaranteed to further culture in the conditions
provided by ScienCell Research Laboratories.
Recommended Medium
It is recommended to use Endothelial Cell Medium (ECM, Cat.
No. 1001) for the culturing of HIMEC in vitro.
Product Use
HIMEC are for research use only. It is not approved for human or
animal use, or for application in in vitro diagnostic procedures.
Storage
Directly and immediately transfer cells from dry ice to liquid nitrogen
upon receiving and keep the cells in liquid nitrogen until cell
culture needed for experiments.
Shipping
Dry ice.
Reference
[1]. Ogawa, H., Rafiee, P., Heidemann, J., Fisher, P. J., Johnson,
N. A., Otterson, M. F., Kalyanaraman, B., Pritchard, K. A. Jr.,
Binion, D. G. (2003) Mechanisms of endotoxin tolerance in human
intestinal microvascular endothelial cells. J Immunol. 170(12):5956-64.
[2]. Binion, D. G., Fu, S., Ramanujam, K. S., Chai, Y. C., Dweik,
R. A., Drazba, J. A., Wade, J. G., Ziats, N. P., Erzurum, S. C.
and Wilson, K. T. (1998) iNOS xpression in human intestinal microvascular
endothelial cells inhibits leukocyte adhesion. Am. J. Physiol.
275:G592-603.
[3]. Chi, J-T, Chang, H. Y., Haraldsen, G., Jahnsen, F. L., Troyanskaya,
O. G., Chang, D. S., Wang, Z., Rockson, S. G., van de Rijn, M.,
Botstein, D. and Brown, P. O. (2003) Endothelial cell diversity
revealed by global expression profiling. PNAS 100(19):10623-10628.
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