PIEC Cells
USD$800.00*
Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 106 cells for adherent lines or 5 × 106 cells for suspension lines (refer to the batch CoA for details).
General information
| Description | PIEC (Porcine Iliac Endothelial Cells) is a spontaneously immortalized endothelial cell line derived from the iliac artery endothelium of a young pig. The cell line exhibits a typical cobblestone morphology when grown to confluence and forms adherent monolayers under standard culture conditions. PIECs retain key endothelial characteristics, including contact inhibition, expression of endothelial markers such as von Willebrand factor (vWF), and the ability to form capillary-like structures in appropriate in vitro assays. Due to their vascular origin, PIECs are widely used as a model for studying porcine endothelial biology and host-pathogen interactions. Functionally, PIECs display features consistent with macrovascular endothelial cells, including responsiveness to inflammatory stimuli and the capacity to express adhesion molecules involved in leukocyte recruitment. They have been extensively utilized in virology research, particularly for the propagation and study of porcine viruses such as classical swine fever virus (CSFV), African swine fever virus (ASFV), and porcine reproductive and respiratory syndrome virus (PRRSV). Their high permissiveness to certain viral infections and stable growth characteristics make them a valuable in vitro system for viral replication studies, antiviral screening, and vaccine research. Beyond infectious disease applications, PIECs serve as a relevant large-animal endothelial model for investigating vascular barrier function, endothelial activation, angiogenesis, and inflammatory signaling pathways. As a porcine-derived endothelial line, PIECs provide translational relevance for comparative cardiovascular research and preclinical studies where porcine models are commonly employed. |
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| Organism | Pig |
| Tissue | Vascular endothelium |
Characteristics
| Morphology | Epithelial |
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| Growth properties | Adherent |
Regulatory Data
| Citation | PIEC (Cytion catalog number 305213) |
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| Biosafety level | 1 |
| NCBI_TaxID | 9823 |
| CellosaurusAccession | CVCL_C0W5 |
Biomolecular Data
Handling
| Culture Medium | RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a) |
|---|---|
| Supplements | Supplement the medium with heat-inactivated 10% FBS |
| 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. |
| Fluid renewal | 2 to 3 times per week |
| 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. |
| Thawing and Culturing Cells |
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| Incubation Atmosphere | 37°C, 5% CO2, humidified atmosphere. |
| 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. |
| 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. |
Quality Control & Molecular Analysis
| 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. |
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Certificate of Analysis (CoA)
| Lot Number | Certificate Type | Date | Catalog Number |
|---|---|---|---|
| 305213-070524 | Certificate of Analysis | 23. May. 2025 | 305213 |