NB9
Cat.No.: CSC-C6501J
Species: Homo sapiens (Human)
Morphology: other
Culture Properties: Adherent/Suspension cells
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Store in liquid nitrogen.
NB9 (also NB-9 or NB9) is a cancer cell line derived from a human neuroblastoma, a solid tumor that affects the sympathetic nervous system. Neuroblastoma most often originates from the adrenal medulla or sympathetic chain and is most common in children. NB9 was developed from the primary tumor tissue of a 5-year-old female neuroblastoma patient. NB9 is tumorigenic and immortalized. NB9, like other neuroblastoma-derived cell lines, has the potential to display variable morphology and expression of tumor-associated genes. NB9 is frequently used to study neuroblastoma pathogenesis and development. NB9 has been used in several studies published on the genetics behind neuroblastic diseases including RAS-related and other oncogenic mutations. NB9 cells may be cultured under typical mammalian tissue culture conditions and maintained in serum-supplemented media (e.g. RPMI-1640 with fetal bovine serum). NB9 cells have properties that allow them to be cultured in suspension or as an adherent monolayer, depending on the application. This cell line is a model for drug screening and pharmacologic testing, genetic perturbation, signaling studies, and other applications related to the study of pediatric neuroblastoma and putative therapeutic interventions.
Effects of Dedifferentiated Fat Cells on Neurogenic Differentiation and Cell Proliferation in Neuroblastoma Cells
Mesenchymal stem cells (MSCs) can induce neuroblastoma (NB) cell differentiation. Dedifferentiated fat cells (DFATs) share properties with MSCs. Here, Hidaka et al. cultured NB cells with DFATs and DFAT-conditioned medium (CM) with or without a PI3K inhibitor, aiming to investigate whether DFATs can induce NB cell differentiation and suppress proliferation.
When observing NB9 cell morphology with a phase-contrast microscope, the co-culture group had more cells with neurites than the control group (Fig. 1a). Quantitative analysis showed a significantly higher percentage of cells with neurite outgrowth in the co-culture group (Fig. 1b). SK-N-SH cells also exhibited similar results (Fig. 1c and d). After confirming NB9 cell differentiation through neurite outgrowth assays, real-time RT-PCR was used to measure mRNA expression of neuronal-specific markers (NF and TUBβ3). Both NB9 and SK-N-SH cells in the co-culture group had significantly higher mRNA levels of NF and TUBβ3 compared to their respective controls (Fig. 1e and f).

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