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Reagenti e strumenti per immunologia, biologia cellulare e biologia molecolare

Jurkat

Stampa

Cat# 302147

Contatta il distributore locale :

Telefono : +1 850 650 7790

Marca : CLS Cell Lines Service

Contatta il distributore locale :

Telefono : +1 850 650 7790

Jurkat Cells

Description	Jurkat cells, which originated from the peripheral blood of a 14-year-old with T-cell acute lymphoblastic leukemia (T-ALL), are a well-known human T lymphocyte cell line commonly used in cell biology studies, particularly in cancer research and immune system disorder investigations. These cells play a crucial role in understanding various cellular processes, including cell death mechanisms, autophagy activity, and cytoplasmic transcription factors. Jurkat cells are commonly used in HIV research due to their expression of the CD4 receptor on their cell membrane. The CD4 receptor is a primary receptor that HIV uses to enter host cells. Because Jurkat cells express this receptor, they can be infected by HIV, making them a useful model for studying HIV's interactions with human T cells, which are a major target of the virus in the human body. The utilization of Jurkat cells in HIV activation and the HIV infection life cycle studies has significantly contributed to understanding the virus's interactions with human cells and has been instrumental in identifying potential targets for antiretroviral therapies. Jurkat cells further play a pivotal role in biomedical research, particularly in the evaluation of cytotoxicity and cell viability assays. This makes them indispensable for testing the effectiveness of potential cancer therapies and agents that modulate the immune response. By employing Jurkat cells, scientists can meticulously analyze the effects of cytotoxic compounds on the integrity and function of the cell membrane, including aspects related to cell membrane permeability and their transport properties. Furthermore, the presence of mutations in the Lck gene within Jurkat cells, which leads to sustained activation of T-cells, provides a unique model for in-depth studies of T-cell activation and signaling pathways. This is essential for understanding the complex processes of lymphocyte activation, which encompasses the cell cycle, cellular growth, and differentiation. Such insights are crucial for developing strategies to modulate immune responses in various diseases. The creation of a specific Jurkat cell derivative, known as Jurkat E6.1, has significantly advanced our comprehension of cellular mechanisms. This derivative offers a refined tool for probing into the nuanced behaviors of cell membranes and the physiological responses of individual cells under experimental conditions. Through the use of Jurkat E6.1 cells, researchers have been able to shed light on fundamental cellular processes and their implications for health and disease. In summary, Jurkat cells serve as invaluable tools in a wide range of research areas, from cancer biology to HIV infection studies, offering insights into cell biology, immune system function, and potential therapeutic interventions.
Organism	Human
Tissue	Blood
Disease	T-cell acute lymphoblastic leukemia
Metastatic site	Peripheral blood
Applications	T-cell biology research, development of T-cell therapies, study of T-cell activation and signaling, drug efficacy testing (e.g., kinase inhibitors), cancer research focusing on T-cell acute lymphoblastic leukemia.
Synonyms	JURKAT, JM, JM-Jurkat, Jurkat-FHCRC, Jurkat FHCRC, FHCRC-11, FHCRC subclone 11, FCCH1024

Age	14 years
Gender	Male
Ethnicity	European
Morphology	Lymphoblast
Growth properties	Suspension

Citation	Jurkat (Cytion catalog number 302147)
Biosafety level	1

Antigen expression	Jurkat cells express T-cell receptor (TCR) and CD3 proteins. They also express CD4 and CD8 co-receptors, which aids in identifying them as helper or cytotoxic T cells.
Mutational profile	The Jurkat cell line has been reported to have genetic mutations primarily impacting three core pathways: TCR signaling, genome stability, and O-linked glycosylation. In TCR signaling, mutations in PTEN, INPP5D, CTLA4, and SYK disrupt normal cellular responses to T-cell receptor activation, potentially affecting proliferation and survival. Genome stability is compromised by mutations in TP53, BAX, and MSH2, leading to impaired DNA repair mechanisms and an increased susceptibility to tumorigenesis. Additionally, a mutation in C1GALT1C1 disrupts O-linked glycosylation processes, resulting in the expression of truncated O-glycans [1]. Additionally, the Jurkat cells have a point mutation in the Lck gene, which encodes a protein necessary for T-cell activation, causing T cells to be constitutively activated. References: 1. Gioia, L., Siddique, A., Head, S. R., Salomon, D. R., & Su, A. I. (2018). A genome-wide survey of mutations in the Jurkat cell line. BMC genomics, 19, 1-13.
Karyotype	The Jurkat cell line is hypotetraploid with a flat modal karyotype of 46 chromosomes and 7.8% polyploidy.

Culture Medium	RPMI 1640, w: 2.1 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a)
Medium supplements	Supplement the medium with 10% heat-inactivated FBS
Doubling time	26 hours
Subculturing	Gently homogenize the cell suspension in the flask by pipetting up and down, then take a representative sample to determine the cell density per ml. Dilute the suspension to achieve a cell concentration of 1 x 10^5 cells/ml with fresh culture medium, and aliquot the adjusted suspension into new flasks for further cultivation.
Split ratio	1:2 to 1:5
Fluid renewal	2 to 3 times per week
Freeze medium	CM-1 (Cytion catalog number 800100) or CM-ACF (Cytion catalog number 806100)
Handling of cryopreserved cultures	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. Optionally, skip centrifugation but remove any remaining freezing medium after 24 hours. 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.

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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