Dietary Cows’ Milk Protein A1 Beta-Casein Increases the Incidence of T1D in NOD Mice

Autor: Christophe Lefevre, Karen M. Dwyer, Sonja Kukuljan, Jennifer L. McRae, Joanne S.J. Chia, Ashwantha Kumar Enjapoori
Rok vydání: 2018
Předmět:
Blood Glucose
Male
0301 basic medicine
medicine.medical_specialty
type 1 diabetes
Regulatory T cell
cows’ milk
lcsh:TX341-641
030209 endocrinology & metabolism
Nod
Biology
T-Lymphocytes
Regulatory

Article
03 medical and health sciences
0302 clinical medicine
Mice
Inbred NOD

Risk Factors
Internal medicine
Diabetes mellitus
Casein
medicine
Animals
Glucose homeostasis
Genetic Predisposition to Disease
Cells
Cultured

NOD mice
Type 1 diabetes
Nutrition and Dietetics
epigenetics
Caseins
beta-casein
medicine.disease
Animal Feed
Coculture Techniques
Gastrointestinal Microbiome
Diabetes Mellitus
Type 1

030104 developmental biology
medicine.anatomical_structure
Endocrinology
Dietary Supplements
Animal Nutritional Physiological Phenomena
Female
Gene-Environment Interaction
lcsh:Nutrition. Foods and food supply
Insulitis
Biomarkers
Food Science
Zdroj: Nutrients, Vol 10, Iss 9, p 1291 (2018)
Nutrients
Volume 10
Issue 9
ISSN: 2072-6643
Popis: The contribution of cows&rsquo
milk containing beta-casein protein A1 variant to the development of type 1 diabetes (T1D) has been controversial for decades. Despite epidemiological data demonstrating a relationship between A1 beta-casein consumption and T1D incidence, direct evidence is limited. We demonstrate that early life exposure to A1 beta-casein through the diet can modify progression to diabetes in non-obese diabetic (NOD) mice, with the effect apparent in later generations. Adult NOD mice from the F0 generation and all subsequent generations (F1 to F4) were fed either A1 or A2 beta-casein supplemented diets. Diabetes incidence in F0&ndash
F2 generations was similar in both cohorts of mice. However, diabetes incidence doubled in the F3 generation NOD mice fed an A1 beta-casein supplemented diet. In F4 NOD mice, subclinical insulitis and altered glucose handling was evident as early as 10 weeks of age in A1 fed mice only. A significant decrease in the proportion of non-conventional regulatory T cell subset defined as CD4+CD25&minus
FoxP3+ was evident in the F4 generation of A1 fed mice. This feeding intervention study demonstrates that dietary A1 beta-casein may affect glucose homeostasis and T1D progression, although this effect takes generations to manifest.
Databáze: OpenAIRE