CELL MODEL DATASHEET

Human iPSC-Derived Endothelial Cells

Human iPSC-Derived Endothelial Cells

Diverse-donor endothelial cells for vascular, barrier and liver co-culture models

Cytochroma human iPSC-derived endothelial cells are cryopreserved endothelial cells differentiated from an ancestrally and genetically diverse, HLA-typed induced pluripotent stem cell library. Endothelium controls the barrier between blood and tissue, so it governs how much of a compound reaches its target and how immune cells traffic into an inflamed organ. Supplying endothelial cells from the same genotyped donors as Cytochroma hepatocytes and Kupffer cells allows vascularised and sinusoid-like liver models to be built in one consistent genetic background.

8 / 18

donor lines fully HLA-typed

71

distinct HLA alleles across the panel

1:1

female to male donor balance

3

Mapped to 3 diverse ancestry groups

Why this model

IComplete the microenvironment

Endothelial cells add the vascular compartment to hepatic co-cultures and microtissues, alongside hepatocytes, Kupffer cells and hepatic stellate cells from the same donor library.

Genotype-matched or deliberately mismatched

With HLA typing at two-field resolution across eight lines, endothelial and immune compartments can be matched or mismatched on purpose for allogeneic and vascular immune studies.

Renewable supply

Differentiated to order from a defined iPSC library rather than sourced from scarce primary donor tissue.

specifications


Cell type

Human iPSC-derived endothelial cells

Donor panel

8 of 18 lines fully HLA-typed at two-field resolution; 71 distinct HLA alleles; 1:1 female to male

Viable cells per vial

Greater than or equal to 1 x 10⁶ (1.63 x 10⁶ recorded for lot MAN019-31E)Post-thaw viability

Post-thaw viability

70% by automated trypan blue exclusion; 96.0% recorded for lot MAN019-31E

Format

Cryopreserved, 1.0 mL per vial; store at or below -145 °C; 12 months from receipt

Identity markers

CD31 (PECAM-1) detected by immunofluorescence at QC4; polygonal endothelial morphology confirmed by microscopy. CD144 (VE-cadherin) and CD34 also detected by immunofluorescence.

Functional characterisation

Dil-Ac-LDL uptake demonstrated at QC4 (10 µg/mL, 1 hour, 37 °C). Forms capillary-like networks in three-dimensional spheroid culture, with continuous CD144 junctional staining consistent with adherens-junction formation.

Documentation

Certificate of Analysis with every lot: viability, viable recovery, mycoplasma (MycoAlert, ratio less than 1.0), bacterial and fungal sterility, adherence at 24 hours, morphology, Dil-Ac-LDL uptake and CD31 staining, with brightfield and fluorescence images.

Sterility and mycoplasma

Mycoplasma negative by MycoAlert activity assay (ratio less than 1.0); bacteria and fungi negative by visual assessment at QC4

Manufactured in

Roslin Innovation Centre, Edinburgh, United Kingdom


Phenotype and imaging

Representative immunofluorescence from Cytochroma production batches. Full imaging data and batch-specific Certificates of Analysis are available on request.


Immunofluorescence micrograph of Cytochroma human iPSC-derived hepatocytes stained for albumin in green with nuclei counterstained blue, showing cobblestone morphology and frequent binucleation. Albumin immunostaining (green) with nuclear counterstain (blue). Cobblestone morphology and binucleate cells are hallmarks of mature hepatocyte identity, not the flat, fetal-like phenotype typical of immature iPSC-hepatocyte protocols.

CD31 (PECAM-1) in green, localised to cell–cell junctions with nuclei counterstained blue. CD31 is the canonical endothelial identity marker.

CD144 (VE-cadherin) in green. Continuous junctional staining indicates formation of adherens junctions and a competent endothelial barrier.

Bile canalicular network visualised by MRP1 immunostaining (red) between adjacent hepatocytes. Visible canaliculi indicate apical–basal polarisation, which is what makes hepatic transporter and efflux studies physiologically meaningful.

Three-dimensional network formation. Endothelial cells organise into capillary-like structures within a spheroid, the basis for vascularised liver microtissue and organ-on-chip models.

Lipid-loaded hepatocytes in the MAFLD/MASH model. Neutral lipid droplets (green) are quantified by high-content imaging as total lipid area and droplet size. CYP450 function is maintained throughout disease induction

Applications

  • Vascularised liver microtissue and organ-on-chip models

  • Barrier integrity and permeability studies

  • Endothelial activation and immune cell adhesion assays

  • Angiogenesis and tube formation assays

  • Donor-stratified vascular toxicity screening

  • Co-culture with iPSC-derived hepatocytes, Kupffer cells and stellate cells

Donor diversity and HLA typing

Every Cytochroma cell model is differentiated from an induced pluripotent stem cell library built deliberately for population-level variability rather than convenience. 8 of 18 of 18 iPSC donor lines fully HLA-typed at two-field resolution. 71 distinct HLA alleles across the panel. 1:1 female to male donor balance. European, Native American and African ancestry represented. Pairwise HLA mismatch scores of 7 to 10 out of 10 between almost every donor pair, across HLA-A, B, C, DRB1 and DQB1.

Typing covers the classical class I loci HLA-A, HLA-B and HLA-C and the class II loci DRB1, DRB3/4/5, DQA1, DQB1, DPA1 and DPB1 at two-field resolution. Full multi-field typing is available on request. Because almost every donor pair scores 7 to 10 out of 10 on pairwise allele-level mismatch, donor-mismatched co-culture, allogeneic response and HLA-restriction studies can be set up off the shelf.

Evidence and validation

PShared donor library

Endothelial cells draw on the same HLA-typed, ancestrally diverseiPSC library documented for the Cytochroma hepatic range.

Frequently asked questions

What are iPSC-derived endothelial cells used for?
Are the endothelial donor lines HLA-typed?
Can endothelial cells be supplied from the same donor as the hepatocytes?
How do I order?

Request a quote or technical discussion

Tell us your assay format, donor requirements, and timelines. Our scientific team will help select the right donor panel and model configuration.