Immortalized Human Brain Microvascular Endothelial Cells

Cat.No.: CSC-I9355Z

Species: homo sapiens

Morphology: Polygonal

Culture Properties: Adherent

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Cat.No.
CSC-I9355Z
Description
Immortalized Human Brain Microvascular Endothelial Cells-SV40 were derived from Primary Human Brain Microvascular Endothelial Cells transduced with a lentiviral expression vector containing the SV40T gene. The cell line was continuously cultured for more than 20 passages without showing signs of growth retardation or replicative senescence.
Species
homo sapiens
Recommended Medium
SuperCult® Immortalized Human Brain Microvascular Endothelial Cell Medium (Cat No.: CM-I9005L)
Freezing Medium
Complete medium supplemented with 10% (v/v) DMSO
Culture Properties
Adherent
Morphology
Polygonal
Immortalization Method
SV40 large T antigen
Application
For Research Use Only
Growth Properties
Cells are cultured as a monolayer at 37°C in a humidified atmosphere with 5% CO2.
Shipping
Dry Ice.
Recommended Products
CSC-C1503 Human Brain Microvascular Endothelial Cells
CIK-HT003 HT® Lenti-SV40T Immortalization Kit
Quality Control
Real Time PCR was used to quantify SV40T gene expression in immortalized cell line. Free from contaminations (bacteria incl. mycoplasma, fungi, HIV, HAV, HBV, HCV, Parvo-B19) and cross-contaminations.
Storage and Shipping
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.

Note: Never can cells be kept at -20 °C.
BioSafety Level
II
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

Immortalized Human Brain Microvascular Endothelial Cells (HBMECs) are a commonly utilized in vitro model for studying blood-brain barrier (BBB) cell and molecular biology. The immortalization of human brain microvessel-derived HBMECs utilizes methods including the SV40 large T antigen to promote their extended growth and division capabilities. Morphologically, HBMECs display the characteristic cobblestone-like monolayer typical of microvascular endothelium and express hallmark endothelial markers including CD31, VE-cadherin, vWF, and eNOS. Importantly, they form tight junction structures-such as ZO-1, claudin-5, and occludin-that are essential for modeling the barrier properties of the BBB.

Immortalized HBMECs have been used to study a wide range of BBB cellular and molecular biology properties, such as selective molecular transport, expression of efflux transporters like P-gp and BCRP, inflammatory responses, for example, induction of adhesion molecules such as ICAM-1 and VCAM-1 upon stimulation with inflammatory cytokines. This, along with their physiological relevance, has made them a commonly used model for various applications, including drug permeability assays, neuroinflammation, CNS infection, neurovascular unit, and oxygen-glucose deprivation to mimic ischemia. They are also used in more complex systems, for example in co-culture or microfluidic "BBB-on-a-chip" systems.

Effect of OEC-CM on HBMEC Viability under Normoxic or Hypoxic Conditions

Hypoxia compromises the blood-brain barrier (BBB) integrity and induces inflammation. Olfactory ensheathing cells (OECs) have neuroregenerative and anti-inflammatory properties. Agafonova et al. investigated the modulatory effects of OEC-conditioned medium (OEC-CM) on human brain microvascular endothelial cells (HBMECs) under hypoxia.

The effect of OEC-CM treatment on the proliferation and viability of HBMECs was assessed using the CCK-8 assay under both normoxic and hypoxic conditions at different time points (6 h, 24 h, and 30 h) (Fig. 1). At the 6 h and 24 h time points, the viability of HBMECs under hypoxic conditions (HYP) in their basal medium closely resembled that of cells in normoxia (CTRL). However, a notable decrease in viability was observed at the 30 h time point. Incubation with OEC-CM under hypoxic conditions (HYP + OEC-CM) at 6 h and 24 h exhibited results comparable to their respective controls in hypoxia, while at 30 h, the viability increased by 1.46-fold compared to the corresponding hypoxic control. Results indicate a significant impact of OEC-CM treatment on HBMEC viability, particularly under long-term hypoxic conditions.

Effect of olfactory ensheathing cell conditioned medium (OEC-CM) on HBMEC viability under normoxic (21% O2, 5% CO2, and 74% N2) or hypoxic conditions (HYP).

Fig. 1. Effect of olfactory ensheathing cell conditioned medium (OEC-CM) on HBMEC viability under normoxic (21% O2, 5% CO2, and 74% N2) or hypoxic conditions (HYP) (1% O2, 5% CO2, and 94% N2) (Agafonova A, Cosentino A, et al., 2025).

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