Spontaneous Incidental Brain Lesions in C57BL/6J Mice

Author:

Tarrant James C.1ORCID,Savickas Patrick1,Omodho Lorna2,Spinazzi Marco3,Radaelli Enrico12ORCID

Affiliation:

1. Department of Pathobiology, University of Pennsylvania School of Veterinary Medicine, Philadelphia, PA, USA

2. VIB Center for the Biology of Disease and KU Leuven Center for Human Genetics, Leuven, Belgium

3. Centre de Référence des Maladies Neuromusculaires, Service de Neurologie, Centre Hospitalier Universitaire d’ Angers, Angers, France

Abstract

Genetically engineered mouse lines on a C57BL/6J background are widely employed as preclinical models to study neurodegenerative human disorders and brain tumors. However, because of the lack of comprehensive data on the spontaneous background neuropathology of the C57BL/6J strain, discriminating between naturally occurring changes and lesions caused by experimental mutations can be challenging. In this context, this study aims at defining the spectrum and frequency of spontaneous brain changes in a large cohort of C57BL/6J mice and their association with specific biological variables, including age and sex. Brains from 203 experimentally naive and clinically unremarkable C57BL/6J mice were collected and analyzed by means of histopathology and immunohistochemistry. Mice ranged in age from 3 to 110 weeks with 89 females, 111 males, and 3 unknowns. Sixteen different spontaneous lesion categories were described in this cohort. Age-related neurodegenerative and/or neuroinflammatory findings represented the most common pathologic changes and included (1) Hirano-like inclusions in the thalamic neurons, (2) neuroaxonal dystrophy in the medulla oblongata, (3) periodic acid–Schiff–positive granular deposits in the neuropil of the hippocampus, and (4) progressive neuroinflammation characterized by microgliosis and astrogliosis. Neoplastic conditions, developmental abnormalities, and circulatory disorders were rarely observed incidental findings. In conclusion, this study describes spontaneous age-related brain lesions of the C57BL/6J mouse and provides a reference for evaluating and interpreting the neuropathological phenotype in genetically engineered mouse models developed and maintained on this congenic background.

Funder

NIH Shared Instrument Grant

Publisher

SAGE Publications

Subject

General Veterinary

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