GL261 luciferase-expressing cells elicit an anti-tumor immune response: an evaluation of murine glioma models.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
03 07 2020
Historique:
received: 13 01 2020
accepted: 03 06 2020
entrez: 5 7 2020
pubmed: 6 7 2020
medline: 15 12 2020
Statut: epublish

Résumé

Preclinical models that reliably recapitulate the immunosuppressive properties of human gliomas are essential to assess immune-based therapies. GL261 murine glioma cells are widely used as a syngeneic animal model of glioma, however, it has become common practice to transfect these cells with luciferase for fluorescent tumor tracking. The aim of this study was to compare the survival of mice injected with fluorescent or non-fluorescent GL261 cells and characterize the differences in their tumor microenvironment. Mice were intracranially implanted with GL261, GL261 Red-FLuc or GL261-Luc2 cells at varying doses. Cytokine profiles were evaluated by proteome microarray and Kaplan-Meier survival analysis was used to determine survival differences. Median survival for mice implanted with 5 × 10

Identifiants

pubmed: 32620877
doi: 10.1038/s41598-020-67411-w
pii: 10.1038/s41598-020-67411-w
pmc: PMC7335060
doi:

Substances chimiques

Cytokines 0
Luciferases EC 1.13.12.-

Types de publication

Journal Article Research Support, N.I.H., Intramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

11003

Commentaires et corrections

Type : ErratumIn

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Auteurs

Victoria E Sanchez (VE)

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

John P Lynes (JP)

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Stuart Walbridge (S)

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Xiang Wang (X)

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Nancy A Edwards (NA)

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Anthony K Nwankwo (AK)

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Hannah P Sur (HP)

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Gifty A Dominah (GA)

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Arnold Obungu (A)

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Nicholas Adamstein (N)

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Pradeep K Dagur (PK)

Flow Cytometry Core Facility, National Heart, Lung, and Blood Institute, Bethesda, MD, USA.

Dragan Maric (D)

Flow Cytometry Core Facility, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Jeeva Munasinghe (J)

Mouse Imaging Facility, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

John D Heiss (JD)

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Edjah K Nduom (EK)

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA. edjah.nduom@nih.gov.
Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, NIH, Room 3D-20, 10 Center Drive, Bethesda, MD, 20892, USA. edjah.nduom@nih.gov.

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Classifications MeSH