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HMEC-1
Tissue
Skin
Synonyms
Hmec-1, HMEC1, CDC/EU.HMEC-1, Human Microvascular Endothelial Cell line-1

Documents

HMEC-1

Cell line · Product number 304064

HMEC-1 cells, or Human Microvascular Endothelial Cells-1, are an immortalized cell line derived from human dermal microvascular endothelial cells. This ce...

CA$759.00excl. tax and shipping
In stock
Lot
Recommended (freshest lot)
  • CoA
1

01General information

Description

HMEC-1 cells, or Human Microvascular Endothelial Cells-1, are an immortalized cell line derived from human dermal microvascular endothelial cells. This cell line was developed to facilitate research on the microvascular endothelial function and pathology. HMEC-1 cells are extensively used in vascular biology research due to their ability to retain many of the phenotypic and functional characteristics of primary endothelial cells.

HMEC-1 cells display typical endothelial cell markers such as CD31 (PECAM-1), von Willebrand factor, and VE-cadherin, and they can form capillary-like structures when cultured on appropriate matrices, mimicking angiogenesis in vitro. This makes them particularly valuable for studies on angiogenesis, the formation of new blood vessels from pre-existing vasculature, a critical process in both physiological and pathological conditions such as wound healing, cancer growth, and cardiovascular diseases.

These cells are also used to explore endothelial cell responses to inflammatory cytokines, the barrier function of endothelial layers, and the interaction between endothelial cells and other cell types like immune cells. HMEC-1 cells are amenable to genetic manipulation, allowing researchers to investigate the impact of specific genes on endothelial function and to model various vascular diseases.

Furthermore, HMEC-1 cells serve as a model system for studying the permeability of endothelial barriers, which is crucial in the context of drug delivery and the pathogenesis of infectious diseases where pathogens cross endothelial barriers. The cell line’s versatility and ease of use continue to make it a cornerstone in studies of microvascular endothelial cell biology and pathology.

Tissue
Skin
Applications
Research studies for human dermal endothelial cells
Synonyms
  • Hmec-1
  • HMEC1
  • CDC/EU.HMEC-1
  • Human Microvascular Endothelial Cell line-1

02Classification

Organism
Human
Sex
Male
Growth properties
Adherent
GMO status
GMO-S1
GMO status details
GMO-S1: This human microvascular endothelial cell line (HMEC-1) contains an SV40 T-Antigen construct delivered via the pSVT vector, enabling robust proliferation and immortalization. The construct is stably integrated into endothelial cells. This classification applies only within Germany and may differ elsewhere.
Biosafety level
1

03Characteristics

Morphology
Endothelial-like

04Identifiers

Citation
HMEC-1 (Cytion catalog number 304064)
NCBI TaxID
9606
Cellosaurus
CVCL_0307

05Expression and susceptibility

Protein expression
Von Willebrand's factor (vWF), cell adhesion molecules ICAM-1
Viruses
Simian virus 40 (large T antigen)

06Handling and culture

Culture medium
Alpha MEM, w: 2.0 mM stable Glutamine, w/o: Ribonucleosides, w/o: Deoxyribonucleosides, w: 1.0 mM Sodium pyruvate, w: 2.2g/L NaHCO3
Incubation atmosphere

37°C, 5% CO2, humidified atmosphere.

Supplements
Supplement the medium with 10% FBS, 10 ng/mL Epidermal Growth Factor, 1 microgram/mL Hydrocortisone, 10 mM Glutamine
Dissociation reagent
Accutase
Subculturing
Remove the old medium from the adherent cells and wash them with PBS that lacks calcium and magnesium. For T25 flasks, use 3-5 ml of PBS, and for T75 flasks, use 5-10 ml. Then, cover the cells completely with Accutase, using 1-2 ml for T25 flasks and 2.5 ml for T75 flasks. Let the cells incubate at room temperature for 8-10 minutes to detach them. After incubation, gently mix the cells with 10 ml of medium to resuspend them, then centrifuge at 300xg for 3 minutes. Discard the supernatant, resuspend the cells in fresh medium, and transfer them into new flasks that already contain fresh medium.
Thawing and culturing
  1. Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit.

  2. 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.

  3. 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.

  4. Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening.

  5. 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.

  6. Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium.

  7. 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.

  8. 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 complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, 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
1 month