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UK Health Security Agency

U-373 MG (Uppsala)

U-373 MG (Uppsala)

Catalogue No.

08061901

Cell Line Name

U-373 MG (Uppsala)

Cell Line Description

A human glioblastoma astrocytoma derived from a malignant tumour by explant technique. This catalogue entry represents a new deposit of U-373 MG obtained from the originator's laboratory in Uppsala; it has been designated U-373 MG (Uppsala) to distinguish it from U-373 MG (ECACC catalogue number 89081403) which is now known to be identical, by Short Tandem Repeat (STR)-PCR profiling, to another glioblastoma cell line, U-251 MG (please read below for more information about this discovery). U-373 MG (Uppsala) has been mycoplasma eradicated at ECACC and the stocks available for supply have undergone a further 10 passages without detection of mycoplasma. Background to the identity query for the cell line U-373 MG: The American Type Culture Collection (ATCC) reported that their stock of U-373 MG had been shown to have differing genetic properties to stock from the originator's laboratory, and to share similarities with another glioblastoma cell line, U-251. In light of this, ECACC undertook an investigation into the authenticity of its own stock of the U-373 MG cell line. ECACC found similar results to the ATCC i.e. the stock held as U-373 MG was found to be identical by STR-PCR profiling to U-251. The U-373 MG cell line listed under catalogue number 89081403 has been re-named as ‘U-251 (formerly known as U-373 MG)'.

Characteristics

Receptors

PDGFR alpha and EGFR. See Nistér M. et al., (1988) & (1991)

Products

Contains GFAP positive cells

Tissue of Origin

Brain

DNA profile (STR Profile)

Amelogenin: X
CSF1PO: 11,12
D5S818: 12
D7S820: 8.2,12
D13S317: 8
D16S539: 12,13
TH01: 7,9.3
TPOX: 8
vWA: 17,18

Karyotype

2n = 46

Disease

None Stated

Culture Conditions

Cell Type

Pleomorphic, Astrocytoid

Subculture Routine

Split sub-confluent cultures (70-80%) 1:3 to 1:6 i.e. seeding at 2-4x10,000 cells/cm² using 0.05% trypsin or trypsin/EDTA; 5% CO₂; 37°C.

Culture Medium

EMEM (EBSS) + 2mM Glutamine + 1% Non Essential Amino Acids (NEAA) + 1mM Sodium Pyruvate (NaP) + 10% Foetal Bovine Serum (FBS).

Growth Mode

Adherent

Additional Info

Depositor

Professor Bengt Westermark, Department of Genetics and Pathology, University Hospital, S-751 85 Uppsala, Sweden.

Country of Origin

Sweden

Hazard Group (ACDP)

Hazard Group (ACDP) 2

Applications

References

Pontén, J., Macintyre, E. H. (1968) Long term culture of normal and neoplastic human glia. Acta Pathol Microbiol Scand A. 74, 465-486 PMID: 4313504.

Bibliography

Westermark B. et al., (1973) Determinants for the establishment of permanent tissue culture lines from human gliomas. Acta Pathol Microbiol Scand A. 81:791-805. PMID: 4359449. Pontén, J. & Westermark B. (1978) Properties of Human Malignant Glioma Cells in Vitro. Medical biology 56: 184-193 PMID: 359950.Nistér M. et al., (1988) Expression of messenger RNAs for platelet-derived growth factor and transforming growth factor-alpha and their receptors in human malignant glioma cell lines. Cancer Res. Jul 15; 48(14):3910-8 PMID: 2454731.Nistér M. et al., (1991) Differential expression of platelet-derived growth factor receptors in human malignant glioma cell lines. J Biol Chem. Sep 5; 266(25):16755-63 PMID: 1653246.

Available Formats

  • Frozen
  • DNA-5µg (100ng/µl)

If use of this culture results in a scientific publication, it should be cited in the publication as: U-373 MG (Uppsala) (ECACC 08061901).

Unless specified otherwise, at ECACC we routinely handle all of our cell lines at containment level 2 in accordance with the ACDP guidelines (Advisory Committee on Dangerous Pathogens) (UK). All cell cultures have the potential to carry as yet unidentified adventitious agents. It is the responsibility of the end user to ensure that their facilities comply with biosafety regulations for their own country. ACDP Guidance: Biological agents: Managing the risks in laboratories and healthcare premises.

The Culture Collections represent deposits of cultures from world-wide sources. While every effort is made to ensure details distributed by Culture Collections are accurate, Culture Collections cannot be held responsible for any inaccuracies in the data supplied. References where quoted are mainly attributed to the establishment of the cell culture and not for any specific property of the cell line, therefore further references should be obtained regarding cell culture characteristics. Passage numbers where given act only as a guide and Culture Collections does not guarantee the passage number stated will be the passage number received by the customer.

Cultures supplied by Culture Collections are for research purposes only. Enquiries regarding the commercial use of a cell line are referred to the depositor of the cell line. Some cell lines have additional special release conditions such as the requirement for a material transfer agreement to be completed by the potential recipient prior to the supply of the cell line. Please view the Terms & Conditions of Supply for more information.