E2F-1-Deficient NOD/SCID Mice Developed Showing Decreased Saliva Production

Author:

Matsui-Inohara Hikaru1,Uematsu Hiroshi1,Narita Takanori1,Satoh Keitaro1,Yonezawa Hideo1,Kuroda Koichiro1,Ito Tatsuro1,Yoneda Saori1,Kawarai Taketo1,Sugiya Hiroshi1,Watanabe Haruo1,Senpuku Hidenobu1

Affiliation:

1. Department of Gerodontology, Graduate School, Tokyo Medical and Dental University, Tokyo 113-8549, Japan; Department of Bacteriology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan; Department of Physiology, Nihon University School of Dentistry at Matsudo, Chiba 271-8587, Japan; Division of Medical Microbiology, Department of Infectious Diseases, Kyorin University School of Medicine, Tokyo 181-8611, Japan; and Department of Bacteriology, Nihon University School of Dentistry, Tokyo 101...

Abstract

The non-obese diabetic mouse (NOD) is the most characterized model used to study insulin-dependent type 1 diabetes mellitus (IDDM) and Sjoögren’s syndrome (SS). In a previous report, we found NOD. E2f1−/−mice show a greater progressive development to IDDM and SS compared to NOD mice. Our previous data indicated a progressive decrease in regulatory T cells (CD4+CD25+) and a decrease in the systemic secretion systems for insulin, and saliva was associated with the progression of IDDM and SS. Therefore, to define the mechanism of early-onset IDDM SS in E2F-1 deficient NOD mice required further investigation by producing E2F-1 deficient NOD/SCID mice in which the T and B cells do not develop. The purpose here was to analyze the essential function of the E2F-1 molecule in the development of IDDM and SS; and the dysfunction of the pancreas islet and salivary gland in the NOD background using NOD/SCID mice. We produced NOD/SCID. E2f1−/−mice using homologous recombination; determined diabetes development; measured saliva and insulin production; and performed a histological analysis. The deficient mice showed a decreasing volume of saliva; no infiltration of lymphocytes into salivary glands; no development of diabetes; and no protein localization of FGFR-2b in the ducts of the salivary gland that regulates submandibular gland proliferation and morphogenesis. Therefore, we considered a deficiency in E2F-1 induces a decrease in regulatory T cells and an increase in auto-reactive T cells; however, the E2F-1 deficiency is not associated with T and B cells-independent dysfunction of pancreatic β cell in insulin secretion. Further, the E2F-1 deficiency is associated with T and B cells-independent dysfunction of the salivary gland exhibits a decrease in saliva production volume. We suggest E2F-1 may be also associated with the differentiation of exocrine cells in the duct where FGFR-2b is expressed in the salivary gland. The E2F-1 deficient NOD/SCID mouse model is useful for showing the development of the salivary gland; and is also useful for various experiments in humanized mice.

Publisher

SAGE Publications

Subject

General Biochemistry, Genetics and Molecular Biology

Reference51 articles.

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