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- Tissue
- Brain, temporal lobe, blood microvessel
- Disease
- Normal cerebral microvascular endothelium (hTERT and SV40-immortalized; blood-brain barrier model; non-tumorigenic)
- Metastatic site
- Not applicable (normal brain endothelial cell line; not a tumor sample)
- Synonyms
- HCMEC/D3, CMEC/D3, human Cortical Microvessels Endothelial Cells/D3
Documents
hCMEC/D3
Cell line · Product number 305024
The HCMEC/D3 cell line represents an immortalized human cerebral microvascular endothelial cell line, extensively utilized in the study of the blood-brain...
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- hCMEC/D3Cell line€800.00
Recommended (freshest lot)
01General information
- Description
The HCMEC/D3 cell line represents an immortalized human cerebral microvascular endothelial cell line, extensively utilized in the study of the blood-brain barrier (BBB). This cell line was generated through the transduction of primary human cerebral microvascular endothelial cells with a lentiviral vector expressing human telomerase reverse transcriptase (hTERT), a crucial enzyme for maintaining telomere length and thereby promoting cellular longevity without transforming the cell phenotype. The introduction of hTERT helps these cells to bypass the replicative senescence that limits the lifespan of primary cells, allowing sustained propagation in culture.
HCMEC/D3 cells retain key physiological and morphological characteristics of primary cerebral endothelial cells, making them a valuable model for in vitro studies of the BBB. These include the expression of tight junction proteins such as claudin-5, occludin, and zonula occludens-1, which are critical for maintaining barrier integrity. The cells also express various transporters and receptors typical of the cerebral endothelium, supporting their use in studies related to drug delivery and neurovascular disorders. The ability of HCMEC/D3 to form a tight monolayer with high electrical resistance underscores their suitability for BBB permeability assays.
Research utilizing HCMEC/D3 cells has covered a wide range of applications, including the investigation of cerebral pathologies such as stroke, multiple sclerosis, and metastasis of cancer to the brain. Their compatibility with various molecular biology techniques also makes them an excellent tool for studying endothelial cell responses to inflammatory stimuli, shear stress, and neurotoxic substances. This cell line provides a robust, reproducible platform for dissecting the molecular events at the cerebral endothelial level, contributing valuable insights into the complexities of neurovascular health and disease.
- Tissue
- Brain, temporal lobe, blood microvessel
- Disease
- Normal cerebral microvascular endothelium (hTERT and SV40-immortalized; blood-brain barrier model; non-tumorigenic)
- Metastatic site
- Not applicable (normal brain endothelial cell line; not a tumor sample)
- Applications
- Blood-brain barrier (BBB) research; neuroinflammation; drug CNS delivery and permeability; transendothelial migration; tight junction biology (claudin-5, occludin, ZO-1); neurological disease modeling; shear stress responses; neurotoxicity testing
- Synonyms
- HCMEC/D3
- CMEC/D3
- human Cortical Microvessels Endothelial Cells/D3
02Classification
- Organism
- Human
- Sex
- Female
- Growth properties
- Adherent
- GMO status
- GMO-S1
- GMO status details
- GMO-S1: This human microvascular endothelial cell line (hCMEC/D3) contains lentiviral constructs encoding SV40 T-Antigen or hTERT, supporting stable immortalization. The insert is integrated into primary endothelial cells. This classification applies only within Germany and may differ elsewhere.
- Biosafety level
- 1
03Characteristics
- Morphology
- Endothelial-like (cobblestone)
- Cell type
- Endothelial cell
- Doubling time
- approx. 24 to 36 hours
04Identifiers
- Citation
- hCMEC/D3 (Cytion catalog number 305024)
- NCBI TaxID
- 9606
- Cellosaurus
- CVCL_U985
05Expression and susceptibility
- Viruses
- Transformant: Simian virus 40 (SV40)
06Handling and culture
- Culture medium
- EGM -2 MV Microvascular Endothelial Cell Growth Medium-2 BulletKit (from Lonza, Lonza catalog number CC-3202)
- Incubation atmosphere
37°C, 5% CO2, humidified atmosphere.
- Supplements
- Supplement the supplied EBM-2 Basal Medium as recommended by the manufacturer
- Dissociation reagent
- Accutase or 0.25% Trypsin-EDTA (brief; do not over-trypsinize)
- Subculturing
- Remove medium, wash with PBS without Ca²⁺/Mg²⁺, add Accutase (3–5 min at 37°C), neutralize with complete medium, centrifuge 300×g 5 min, reseed at 1–2 × 10⁴ cells/cm² onto collagen-coated flasks.
- Split ratio
- 1 to 3
- Seeding density
- 1 to 2 × 10⁴ cells/cm² (on collagen I-coated surfaces)
- Fluid renewal
- Every 1 to 2 days
- Thawing and culturing
Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit.
Upon receipt, either store the cryovial immediately at temperatures below -150°C to ensure the preservation of cellular integrity, or proceed to step 3 if immediate culturing is required.
For immediate culturing, swiftly thaw the vial by immersing it in a 37°C water bath with clean water and an antimicrobial agent, agitating gently for 40-60 seconds until a small ice clump remains.
Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening.
Carefully open the disinfected vial and transfer the cell suspension into a 15 ml centrifuge tube containing 8 ml of room-temperature culture medium, mixing gently.
Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium.
Gently resuspend the cell pellet in 10 ml of fresh culture medium. For adherent cells, divide the suspension between two T25 culture flasks; for suspension cultures, transfer all the medium into one T25 flask to promote effective cell interaction and growth.
Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes.
07Quality control and cryopreservation
- Sterility
Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods.
To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections.
- Freeze medium
- As a cryopreservation medium, we use 50% basal medium + 40% FBS + 10% DMSO, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress.
- Storage conditions
For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen.
- Shipping conditions
Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage.
08Donor
- Donor age
- Adult
- Ethnicity
- Not specified
09Legal and safety
- Safety precautions
- When planning to store a cryovial in liquid nitrogen for future thawing, it is mandatory to adhere to stringent safety measures. Appropriate protective gloves and clothing are essential, and the use of a face mask or safety goggles is required during the transfer of frozen samples to or from the liquid nitrogen tank. This is to mitigate the risk of injury from potential cryovial explosions upon removal, which can result in the projection of sharp fragments.
- Warranty
At Cytion, we stand behind the quality and viability of our products. We guarantee that our cells will be viable at the start of culture for 60 days after shipment from our facilities. We assure that all materials conform to the specifications described in the Certificate of Analysis and/or Product Sheet.
For full details, please refer to our Warranty Statement.
- Material Transfer Agreement required
- Yes