| General Information |
| Organism |
Homo sapiens, human |
| Cell Line Description |
HEL is a human erythroleukemia cell line established in 1980 by T. Papayannopoulou and her colleagues. This cell line was isolated from the peripheral blood of a 30-year-old male patient who was experiencing a relapse of acute myeloid leukemia (classified as AML M6 / erythroleukemia) following initial treatment for Hodgkin lymphoma. In the field of hematology, HEL cells are widely recognized as the preferred model for studying erythroid differentiation and globin gene regulation. Notably, it was the first human cell line demonstrated to be capable of both spontaneous and inducible globin synthesis. Furthermore, this cell line serves internationally as a leading model system for investigating myeloproliferative neoplasms (MPNs), as it naturally harbors a homozygous JAK2 V617F mutation, which drives the constitutive activation of the JAK-STAT pathway. |
| Tissue |
Myeloid; Peripheral Blood |
| Disease |
Acute Myeloid Leukemia (AML FAB M6; Erythroleukemia) |
| Morphology |
Lymphoblast-like; round, large to occasionally giant multinucleated cells |
| Gender |
Male |
| Age |
30 years |
| Product Format |
Frozen |
| Growth Mode |
Suspension (with a very small fraction of cells loosely adhering to the plastic surface) |
| Biosafety Level |
1 (Biosafety classification is based on U.S. Public Health Service Guidelines) |
| Applications |
1. Molecular pathology of JAK2 V617F-driven myeloproliferative neoplasms (MPNs); 2. Elucidation of the molecular mechanisms regulating hemoglobin switching and erythroid differentiation; 3. Development of models for phorbol ester (e.g., TPA/PMA)-induced macrophage-like lineage switching; 4. Preclinical drug screening of novel JAK2 kinase inhibitors and targeted anti-leukemic compounds; 5. Assessment of epigenetic and gene-silencing modifiers in erythroid malignancies. |
| Shipped In |
Dry ice |
| Storage Temperature |
−196°C (Liquid nitrogen vapor phase) |
| Characteristics |
| Tumorigenic |
Yes, displays engraftment and leukemic development potential in immunocompromised mice |
| Karyotype |
Human hypotriploid karyotype with approx. 2.3% polyploidy; modal chromosome distribution centered at 63 (60–64)<3n>XYY. |
| Genetic Profile |
1. JAK2 Mutation Status: Carries the classic, homozygous, hyperactivating JAK2 V617F mutation (confirmed via RT-PCR and DNA sequencing). 2. Globin Synthesis: Natively expresses hemoglobin transcripts (specifically, including Gγ, Aγ, ε, ζ, and α globin chains). |
| Immunophenotype |
Positive for CD13, CD33, CD34 (weakly), CD41, CD42 (weakly), CD71, and CD235a (Glycophorin A); Negative for CD3, CD14, CD15, and CD19. |
| Growth Kinetics |
Rapid suspension expansion; doubling time is approximately 36 hours under optimal conditions. |
| Mycoplasma Test |
Negative |
| Culture Conditions and Handling |
| Subculturing |
1. Suspension cultures expand in the form of floating single cells and loose cell aggregates. During routine passaging, enzymatic digestion (trypsinization) is not required. 2. Uniformly collect the cell suspension from a culture vessel that is in the active growth phase, and transfer it to a sterile conical centrifuge tube. 3. Centrifuge at a relative centrifugal force of approximately 200-300 × g (or 1000 rpm) for 5 minutes. 4. Thoroughly aspirate and discard the supernatant medium, ensuring that the cell pellet remains intact. 5. Thoroughly and gently resuspend the cell pellet in pre-warmed, fresh complete growth medium. 6. Inoculate into a new culture vessel. Critical Density Window: The minimum inoculation density should be 0.5 X 10^6 cells/mL. Strictly maintain the working culture concentration between 0.2 X 10^6 and 1.0 X 10^6 cells/mL. Never exceed the maximum saturation threshold of 1.5 X 10^6 cells/mL. |
| Medium Renewal |
Every 2 to 3 days (depending heavily on acidic pH shifts and proliferation rates) |
| Subcultivation Ratio |
Split optimal, dense cultures at a ratio of 1:3 to 1:5 every 3 days. |
| Culture Conditions |
Atmosphere: Air, 95%; CO2, 5%; Temperature: 37°C |
| Cryopreservation |
70% Base RPMI 1640 medium + 20% FBS + 10% DMSO |