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Human TRIB3 Stable Cell Line - U-87 MG

For research use only. Not intended for any clinical use.

Cat. No. :   CSC-RO01407

Host Cell :   U87MG Size :   >1x106 frozen cells/vial

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Cell Line Information

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Gene Information

Cat. No. CSC-RO01407
Description This cell line is engineered to stably express Homo sapiens (human) tribbles pseudokinase 3 (TRIB3) in Human glioblastoma / glioma cell line (U-87 MG). GFP reporter gene is also expressed in this cell line allowing fluorescent tracking of cells.
Product Type Human gene overexpression stable cell line
Target Gene TRIB3
Gene Species Homo sapiens (human)
Host Cell U87MG
Host Cell Species Homo sapiens (Human)
Reporter GFP
Applications 1) investigation of gene function
2) screening and validation of antibodies
Size One vial of frozen cells, typically >1x10^6cells/vial
Stability This cell line is stable at least 10 passages.
Quality Control 1) Real-time qPCR analysis of gene mRNA overexpression level
2) GFP fluorescent detection under fluorescent microscopy
3) mycoplasma detection
Storage Liquid nitrogen
Shipping Dry ice
Revival Rapidly thaw cells in a 37°C water bath. Transfer contents into a tube containing pre-warmed media. Centrifuge cells and seed into a 25 cm2 flask containing pre-warmed media.
Growth Properties Adherent
Mycoplasma Negative
Format One frozen vial containing millions of cells
Storage Liquid nitrogen
Safety Considerations The following safety precautions should be observed.
1. Use pipette aids to prevent ingestion and keep aerosols down to a minimum.
2. No eating, drinking or smoking while handling the stable line.
3. Wash hands after handling the stable line and before leaving the lab.
4. Decontaminate work surface with disinfectant or 70% ethanol before and after working with stable cells.
5. All waste should be considered hazardous.
6. Dispose of all liquid waste after each experiment and treat with bleach.
Ship Dry ice
Gene Name TRIB3
GeneID 57761
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The TRIB3 gene (also known as Tribbles pseudokinase 3) encodes a highly conserved scaffold protein that belongs to the Tribbles pseudokinase family. Although TRIB3 itself lacks intrinsic kinase catalytic activity, it plays a pivotal role as an indispensable intracellular signaling regulator and a key sensor of cellular stress. Under normal physiological conditions, TRIB3 expression is tightly regulated. However, when cells encounter various environmental or intracellular stressors—including endoplasmic reticulum (ER) stress, nutrient deprivation, hypoxia, and oxidative damage—its expression levels are significantly upregulated. TRIB3 functions as a negative regulator of the PI3K/AKT signaling pathway by directly binding to the AKT protein, thereby inhibiting its phosphorylation and subsequent activation. Furthermore, TRIB3 interacts with the ATF4, NF-κB, and MAPK signaling pathways, thereby influencing a wide spectrum of cellular processes, such as glucose homeostasis, insulin sensitivity, cell cycle progression, autophagy, and apoptosis. Given the central role TRIB3 plays at the critical nexus of metabolic regulation and cellular survival, dysregulation of its gene expression is frequently implicated as a key pathogenic factor in numerous human diseases, including Type 2 diabetes, cardiovascular diseases, and various malignancies.

The "Human TRIB3 Stable Cell Line," established within the U-87 MG cellular background, serves as a robust, highly reliable, and standardized in vitro experimental model specifically designed to facilitate in-depth research into this multifunctional pseudokinase. The U-87 MG cell line is a classic and widely utilized human primary glioblastoma cell line, making it an ideal platform for studies in neuro-oncology and brain tumor research. Through the application of advanced gene transduction and screening technologies, this stable cell line has been successfully engineered to achieve sustained and stable expression of the human TRIB3 gene. This consistent and stable pattern of gene expression provides researchers with an ideal experimental platform for conducting a diverse range of downstream applications and investigations. Specifically, the "human TRIB3 stable cell line"—constructed against the background of the U-87 MG cell line—is widely utilized to comprehensively elucidate how the TRIB3 protein, through specific molecular mechanisms, drives pathological processes such as the initiation and progression of glioblastoma, as well as tumor infiltration and metastatic dissemination. Furthermore, this cell line serves as a critical resource in the fields of drug discovery and high-throughput drug screening.

The pseudokinase Tribble 3 (TRIB3) is known to play a regulatory role in cellular responses to various stresses, such as glucose deficiency and endoplasmic reticulum (ER) stress. TRIB3 is upregulated in various cancer tissues and is strongly associated with poor patient prognosis. However, the potential regulatory mechanisms and functions of TRIB3 in glioblastoma (GBM) remain unclear. Here, researchers demonstrated upregulated TRIB3 expression in primary tumor specimens from GBM patients and in in vitro GBM cell lines. In vitro experiments showed that overexpression of specific TRIB3 transcripts promoted cell growth and migration, while knockdown of TRIB3 expression inhibited these cellular processes. Furthermore, the growth-promoting effect of TRIB3 was also demonstrated in a xenograft mouse model. Mechanistic studies further revealed that TRIB3 inhibits autophagy flux, and this inhibition is the reason why TRIB3 silencing induces glioblastoma (GBM) cell proliferation and migration. These findings suggest that TRIB3's inhibition of autophagy flux drives the invasion and proliferation of GBM cells, thus implying that TRIB3 may be a potential novel therapeutic target for glioma.

To investigate the function of TRIB3 in gliomas, researchers constructed TRIB3-overexpressing U251 and U87 GBM cells and verified the overexpression efficiency of TRIB3 using Western blot. CCK-8 assay results showed that the cell viability of TRIB3-overexpressing GBM cells was higher than that of the control group (Figure 1A). Furthermore, the clonogenic ability of TRIB3-overexpressing U251 and U87 GBM cells was promoted. Finally, Transwell migration and scratch assays were performed, showing that the proliferation, migration, and invasion abilities of TRIB3-overexpressing GBM cells were enhanced (Figures 1B-1E).

Figure 1. TRIB3 overexpression promotes the proliferation and migration of GBM cells.Figure 1. TRIB3 overexpression promotes the proliferation and migration of GBM cells. (Tang Z, et al., 2020)

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Customer Reviews
High-quality product

Finding a dependable U-87 MG line overexpressing TRIB3 was crucial for our oncology research. Creative Biogene delivered an outstanding product. The cells are robust, exhibit steady growth rates, and the TRIB3 expression has remained completely stable over months of continuous culture.

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