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Human Pulmonary Microvascular Endothelial
Cells
(HPMEC)
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| Catalog Number: 3000 |
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Cell Specification
The pulmonary microvascular endothelial cells (PMEC) form a semiselective
barrier that is critical for lung gas exchange and regulation of
fluid and solute passage between the blood and interstitial compartments
in the lung. They also have metabolic properties that enable it
to carry out certain important nonrespiratory function. The PMECs
are among the most important targets of reactive oxygen species
elaborated in lung injury [1]. During the course of lung inflammation,
neurohumoral mediators and oxidants act on endothelial cells to
induce intercellular gaps permissive for transudation of proteinaceous
fluid from blood into the interstitium [2]. The increased permeability
leads to the hypoxemia associated with adult respiratory distress
syndrome and noncardiogenic pulmonary edema [3].
HPMEC from ScienCell Research Laboratories are isolated from human
lung tissue. HPMEC are cryopreserved immediately after purification
and delivered frozen. Each vial contains >5 x 105
cells in 1 ml volume. HPMEC are characterized by immunofluorescent
method with antibodies to vWF/Factor VIII and CD31 (P-CAM) and by
uptake of DiI-Ac-LDL. HPMEC are negative for HIV-1, HBV, HCV, mycoplasma,
bacteria, yeast and fungi. HPMEC are guaranteed to further expand
for 10 population doublings at 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 HPMEC in vitro.
Product Use
HPMEC 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] Brigham, K. L. (1990) Oxidant stress and adult respiratory distress
syndrome. Eur Respir J Suppl 11: 482s-484s.
[2] Moore T. M., Chetham P. M., Kelly J. J., Stevens T. (1998) Signal
transduction and regulation of lung endothelial cell permeability.
Interaction between calcium and cAMP. Am J Physiol. 275(2
Pt 1):L203-22.
[3] Kelly JJ, Moore TM, Babal P, Diwan AH, Stevens T, Thompson WJ.
(1998) Pulmonary microvascular and macrovascular endothelial cells:
differential regulation of Ca2+ and permeability. Am J Physiol.
274(5 Pt 1):L810-9.
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