Hyaline Arteriolosclerosis in 30 Strains of Aged Inbred Mice.


Journal

Veterinary pathology
ISSN: 1544-2217
Titre abrégé: Vet Pathol
Pays: United States
ID NLM: 0312020

Informations de publication

Date de publication:
09 2019
Historique:
pubmed: 8 5 2019
medline: 7 1 2020
entrez: 8 5 2019
Statut: ppublish

Résumé

During a screen for vascular phenotypes in aged laboratory mice, a unique discrete phenotype of hyaline arteriolosclerosis of the intertubular arteries and arterioles of the testes was identified in several inbred strains. Lesions were limited to the testes and did not occur as part of any renal, systemic, or pulmonary arteriopathy or vasculitis phenotype. There was no evidence of systemic or pulmonary hypertension, and lesions did not occur in ovaries of females. Frequency was highest in males of the SM/J (27/30, 90%) and WSB/EiJ (19/26, 73%) strains, aged 383 to 847 days. Lesions were sporadically present in males from several other inbred strains at a much lower (<20%) frequency. The risk of testicular hyaline arteriolosclerosis is at least partially underpinned by a genetic predisposition that is not associated with other vascular lesions (including vasculitis), separating out the etiology of this form and site of arteriolosclerosis from other related conditions that often co-occur in other strains of mice and in humans. Because of their genetic uniformity and controlled dietary and environmental conditions, mice are an excellent model to dissect the pathogenesis of human disease conditions. In this study, a discrete genetically driven phenotype of testicular hyaline arteriolosclerosis in aging mice was identified. These observations open the possibility of identifying the underlying genetic variant(s) associated with the predisposition and therefore allowing future interrogation of the pathogenesis of this condition.

Identifiants

pubmed: 31060453
doi: 10.1177/0300985819844822
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

799-806

Auteurs

Timothy K Cooper (TK)

1 Department of Comparative Medicine, Penn State Milton S. Hershey Medical Center, Hershey, PA, USA.
2 Department of Pathology, Penn State Milton S. Hershey Medical Center, Hershey, PA, USA.

Kathleen A Silva (KA)

3 The Jackson Laboratory, Bar Harbor, ME, USA.

Victoria E Kennedy (VE)

3 The Jackson Laboratory, Bar Harbor, ME, USA.

Sarah Alghamdi (S)

4 Computational Bioscience Research Center, King Abdullah University of Science and Technology, Thuwal, Kingdom of Saudi Arabia.

Robert Hoehndorf (R)

4 Computational Bioscience Research Center, King Abdullah University of Science and Technology, Thuwal, Kingdom of Saudi Arabia.

Beth A Sundberg (BA)

3 The Jackson Laboratory, Bar Harbor, ME, USA.

Paul N Schofield (PN)

3 The Jackson Laboratory, Bar Harbor, ME, USA.
5 Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.

John P Sundberg (JP)

3 The Jackson Laboratory, Bar Harbor, ME, USA.

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Classifications MeSH