Hot Products

Immortalized Mouse Microglia (BV2)

Cat.No.: CSC-I2227Z

Species: Mouse

Morphology: Morphology microglial

Culture Properties: Adherent/suspension

  • Specification
  • Background
  • Scientific Data
  • Q & A
  • Customer Review
Cat.No.
CSC-I2227Z
Description
Immortalized Mouse Microglial (BV2) cells have become a popular substitute for primary microglia in many experiments. These cells were derived from C57/BL6 neonatal microglia and immortalized using the v-raf/v-myc-carrying J2 retrovirus. BV2 cells express env gp70, nuclear v-myc, and cytoplasmic v-raf oncogene products on their surface. One of the advantages of BV2 cells is their ability to stimulate other glial cells. When present, BV2 cells cause the translocation of NF-kappaB and expression of IL-6 in astrocytes. This makes BV2 cells useful for studying complex cell-cell interactions in various experimental settings. Over 200 publications have used BV2 cells for pharmacological studies, phagocytosis studies, and immunological discoveries. BV2 cells express functional NADPH oxidase, an enzyme implicated in microglia-induced neuronal damage, for neurodegeneration studies. BV2 cells also express primary microglia markers like CD11b, F4/80, and Iba1. However, unlike primary microglia, unstimulated BV2 cells have an amoeboid, hypertrophied morphology, indicating a highly activated and inflammatory state. This means that BV2 cells may not be ideal for studying the low-dose effects of toxicants on microglial activation. Additionally, there is some doubt whether BV2 cells accurately model primary microglia in culture or the brain. Some studies have compared BV2 cells to primary rat microglia, introducing a bias due to species differences and different analysis methods, such as cytokine ELISAs. However, in another study, BV2 cells induced proteins that matched upregulated genes in primary murine microglia.
Species
Mouse
Recommended Medium
SuperCult® Immortalized Mouse Microglia Medium (Cat No.: CM-I2227Z)
Freezing Medium
Complete medium supplemented with 10% (v/v) DMSO
Culture Properties
Adherent/suspension
Morphology
Morphology microglial
Immortalization Method
v-raf/v-myc-carrying J2 retrovirus
Growth Properties
Cells are cultured as a monolayer at 37°C in a humidified atmosphere with 5% CO2.
Shipping
Dry Ice.
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

The role of microglia in neurodegenerative diseases, toxicology, and immunology is an ever-growing area of biomedical research. Traditional studies often rely on animal models, necessitating many animals for experimentation. However, using a microglia-like cell line, such as BV2 cells, offers a promising alternative by providing a continuous and reproducible source of microglia.

BV2 cells are a unique type of microglial cells derived from C57/BL6 murine, a widely used laboratory mouse strain. These cells are immortalized using the v-raf/v-myc carrying J2 retrovirus, resulting in a stable cell line with unique characteristics.

One of the key advantages of BV2 cells is their ability to retain the morphological and functional characteristics of microglia, the resident immune cells of the central nervous system. Due to the expression of v-raf/v-myc, BV2 cells exhibit an accelerated metabolic and proliferation rate compared to other microglia, making them an ideal tool for various research applications. The expression of nuclear v-myc and cytoplasmic v-RAF oncogene products and the env gp70 antigen on the surface of BV2 cells establish them as a suitable model for studying macrophages. These cells possess morphological, phenotypical, and functional markers similar to macrophages, expanding their potential applications in immunology research.

BV2 cells have proven to be a valid substitute for primary microglia in various experimental settings, facilitating research on neurodegeneration, toxicology, immunity, and cell-cell interactions.

Microglia Increase TMZ Resistance of Glioblastoma Cells

Glioblastoma is the most malignant primary brain tumor. Even with standard treatment comprising surgery followed by radiation and concomitant temozolomide (TMZ) chemotherapy, glioblastoma remains incurable. Glioblastomas are densely infiltrated with tumor-associated microglia and macrophages (TAMs). These immune cells affect the tumor cells in experimental studies and are associated with poor patient survival in clinical studies. The aim of the study was to investigate the impact of microglia on glioblastoma chemo-resistance.

We co-cultured patient-derived glioblastoma spheroids with microglia at different TMZ concentrations and analyzed cell death. Co-culture experiments showed that microglia significantly increased TMZ resistance in glioblastoma cells.

Three spheroid cultures (T87, T78 and T121) treated with TMZ showed reduced cell death after co-culture with BV2 microglia.

Fig. 1. Mouse BV2 immortalized microglia reduce TMZ sensitivity of glioblastoma spheroids (Sørensen, Mia Dahl, et al. 2024).

Conditioned Culture Medium of Bone Marrow Mesenchymal Stem Cells Promotes Phenotypic Transformation of Microglia by Regulating Mitochondrial Autophagy

To study the mechanism by which conditioned medium of bone marrow mesenchymal stem cells (BMSCs-CM) facilitates the transition of pro-inflammatory polarized microglia to an anti-inflammatory phenotype.

BV2 cells, a mouse microglia cell line, were transformed into a pro-inflammatory phenotype using lipopolysaccharide (LPS). After co-culture with BMSCs-CM, the expression of pro-inflammatory microglia-related markers decreased, whereas that of anti-inflammatory microglia markers (CD206 and Arg-1) increased significantly (Fig. 2A). The expression levels of inflammatory factors TNF-α and IL-6 were inhibited, whereas those of anti-inflammatory factors TGF-β and IL-10 were increased (Fig. 2B).

Furthermore, co-culture with BMSCs-CM increased mitophagy-associated protein expression, ATP levels, mitochondrial and lysosomal co-localization in these cells and decreased reactive oxygen species levels (Fig. 3A–3E).

BMSCs-CM changed the phenotype and the expression levels of inflammatory and anti-inflammatory factors in BV2 cells

Fig. 2. BMSCs-CM changed the phenotype and the expression levels of inflammatory and anti-inflammatory factors in BV2 cells (Ji, Hangyu, et al., 2024).

BMSCs-CM promoted mitophagy in LPS-induced BV2 cells.

Fig. 3. Roles of BMSC-CM on mitophagy in LPS-induced BV2 cells (Ji, Hangyu, et al., 2024).
What are Immortalized Mouse Microglia (BV2)?

The BV2 cell line consists of mouse microglial cells that have been immortalized to enable indefinite proliferation. These cells retain many of the functional properties of primary microglia and are widely used as a model for studying microglial behavior in various research contexts.

Do you offer customization or additional services for BV2 cells?

Yes, we offer a range of custom services, including:
Genetic modification (e.g., knockout or knock-in projects).
High-volume cell production for large-scale studies.
Development of custom assays to suit specific research objectives.
Tailored media formulations to enhance specific cellular behaviors.

Ask a Question

Write your own review

For research use only. Not for any other purpose.