Lymphocyte activation gene 3 (LAG3) is a transmembrane protein expressed on the surface of immune cells, notably T cells, where it exerts critical regulatory functions in immune responses. Originally identified in 1990, LAG3 has emerged as a key player in immune modulation, particularly in immune tolerance and suppression. Its interaction with major histocompatibility complex (MHC) class II molecules triggers inhibitory signaling pathways, resulting in the dampening of T cell activation and effector functions.
The establishment of a Human LAG3 Stable Cell Line - HEK293 entails a rigorous process designed to achieve a consistent expression of LAG3 in HEK293 cells, a commonly used cell line in biomedical research. This stable cell line serves as an indispensable tool for investigating the intricate mechanisms underlying LAG3-mediated immune regulation. By meticulously optimizing experimental conditions, researchers have successfully created a reliable platform for probing the functional implications of LAG3 in maintaining immune homeostasis and exploring its potential as a therapeutic target. This achievement represents a significant advancement in our understanding of immune regulation and holds promise for the development of novel immunomodulatory strategies.
Upon binding to Major Histocompatibility Complex Class II (MHCII) or Fibrinogen-like 1 (FGL1), the immune checkpoint receptor Lymphocyte activation gene-3 (LAG3) inhibits T cell function. Researchers investigated the role of LAG3 Stable Cell Line in elucidating the molecular structure and ligand engagement of Lymphocyte activation gene-3 (LAG3), an immune checkpoint receptor inhibiting T cell function. They determined the structures of human and murine LAG3 ectodomains, revealing dimeric assembly and epitope mapping. Insights into LAG3:FGL1 interface and ligand-mediated LAG3 clustering advance LAG3-based drug development, offering potential for disrupting T cell activation.
Figure 1. The role of LAG3 Stable Cell Line was examined by researchers, focusing on the colocalization of LAG3 and MHCII proteins on cell surfaces. LAG3 expression was analyzed using flow cytometry under various stimulations, and HLA-DR expression was assessed. Subsequently, the subcellular localization of LAG-3 and HLA-DR in HuT-78 cells was visualized using confocal microscopy, providing insights into their interaction dynamics. (Ming Q, et al., 2022)
1. Immunotherapy: Employing Human LAG3 Stable Cell Line - HEK293 to investigate immune checkpoint blockade efficacy.
2. Cancer Research: Assessing tumor-infiltrating lymphocyte exhaustion through LAG3 interaction studies.
3. Drug Development: Screening compounds for LAG3-targeted therapies via functional assays with HEK293 cells.
4. Autoimmune Disorders: Modeling LAG3-mediated immunoregulation in autoimmune disease pathogenesis.
5. Infectious Diseases: Studying LAG3 involvement in modulating immune responses to pathogens using HEK293 cells.
6. Translational Medicine: Evaluating LAG3-targeted therapies' efficacy in preclinical models to inform clinical trials.
Customer Q&As
What rationale guided the selection of NCI-H82 cells for establishing the stable CD274/Luc cell line?
A: NCI-H82 cells were likely chosen for their relevance to small cell lung cancer (SCLC) research and their potential to express CD274 (PD-L1) along with luciferase, enabling the study of PD-L1 expression dynamics and its correlation with tumor growth and response to therapy.
How was the stability of CD274/Luc expression verified and maintained in this NCI-H82 stable cell line?
A: Stability was likely confirmed through methods such as luciferase assays, immunoblotting for CD274, or flow cytometry, with continuous monitoring to ensure consistent expression levels over time.
Can you provide insights into the characterization of CD274/Luc expression in the NCI-H82 stable cell line, including its correlation with tumor growth and response to immune checkpoint inhibitors?
A: Characterization may involve analysis of luciferase activity as a surrogate marker for CD274 expression, correlation with tumor growth kinetics in vivo, and response to immune checkpoint blockade using PD-L1 inhibitors.
What quality control measures were implemented during the development of this stable cell line?
A: Quality control likely included validation of stable transgene integration, confirmation of CD274/Luc expression levels, assessment of luciferase activity, and monitoring for phenotypic stability and consistency.
How do the observed functional properties of CD274/Luc in this stable cell line relate to its relevance in studying immune evasion mechanisms and therapeutic strategies in SCLC?
A: Comparative analysis with patient-derived samples or in vivo models helps validate the relevance of CD274/Luc expression in immune evasion, tumor progression, and response to immunotherapy, guiding the development of personalized treatment approaches for SCLC patients.
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Customer Reviews
Consistent LAG3 Stable Cell Line
Exceptional reliability! The Human LAG3 Stable Cell Line in HEK293 cells offers consistent LAG3 expression, ensuring robust results in my immunology and cancer research.
Empowering T cell regulation studies
Empowering advanced investigations! With stable LAG3 expression, I can explore immune checkpoint pathways and T cell regulation mechanisms with confidence, driving scientific innovation.
United Kingdom
10/02/2023
Versatile platform for immune modulation
Impressive versatility! This cell line exceeds expectations, providing a reliable platform for studying LAG3-targeted therapies and immune modulation strategies in cancer immunotherapy.
Streamlined experimental workflows
Streamlining research processes! Its stable expression streamlines experimental workflows, simplifying data interpretation and accelerating scientific discoveries.
Pivotal asset for immune response research
A pivotal asset! The Human LAG3 Stable Cell Line has significantly enhanced my research capabilities, offering valuable insights into LAG3-mediated immune responses and potential therapeutic interventions for cancer.
United Kingdom
03/09/2021
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