Implications of Sm22α-Cre expression in keratinocytes and unanticipated inflammatory skin lesion in a model of atherosclerosis

Author:

Hu Mei1,Hiroyasu Sho23,Granville David J.3ORCID,Kassiri Zamaneh1ORCID

Affiliation:

1. Faculty of Medicine and Dentistry, Department of Physiology, Cardiovascular Research Center, University of Alberta, Edmonton, Alberta, Canada

2. Department of Dermatology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan

3. ICORD Centre and Department of Pathology and Laboratory Medicine, Vancouver Coastal Health Research Institute, University of British Columbia, Vancouver, British Columbia, Canada

Abstract

Although Sm22α-Cre is commonly used to target gene deletion in smooth muscle cells, Sm22α-derived Adam17 deletion resulted in unexpected severe skin lesions following high-fat diet feeding in a model of atherosclerosis. Adam17 deletion by a different SMC driver, Myh11-Cre, did not result in skin lesions in the same atherosclerosis model. Sm22α is highly expressed in keratinocytes, causing ectopic loss of ADAM17 in keratinocytes that caused significant epidermal lesions when combined with a high-fat diet.

Funder

Gouvernement du Canada | CIHR | Institute of Health Services and Policy Research

Heart and Stroke Foundation of Canada

Publisher

American Physiological Society

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Improving rigor and reproducibility in cardiovascular research;American Journal of Physiology-Heart and Circulatory Physiology;2023-10-01

2. SMYD2 regulates vascular smooth muscle cell phenotypic switching and intimal hyperplasia via interaction with myocardin;Cellular and Molecular Life Sciences;2023-08-24

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