The goal of this proposal is to understand why people with diabetes develop a more rapid build-up of plaque in arteries. This problem is commonly called ?atherosclerosis? and it is directly responsible for several types of serious cardiovascular diseases that cause numerous disabilities and premature death. A major reason why diabetic individuals develop severe atherosclerosis early on in life is because of high blood sugar that is also called ?hyperglycemia?. Exactly why hyperglycemia enhances atherosclerosis is not known. Unfortunately, studies of diabetic mice in which hyperglycemia accelerates atherosclerosis also led to increased blood cholesterol levels. Because such added blood cholesterol can itself accelerate atherosclerosis, and because diabetic humans do not always have increased blood cholesterol, how hyperglycemia causes more severe atherosclerosis remains incompletely understood. Work performed in our laboratory led to a new strain of genetically engineered mice in which diabetic hyperglycemia does not further increase blood cholesterol levels. Our latest studies of these diabetic mice reveal that hyperglycemia accelerates atherosclerosis by increasing the number of activated immune cells that accumulate in the blood and the artery wall. We also uncovered that hyperglycemia alters the expression of a class of intracellular molecules called microRNA that can regulate genetic programs in immune cells making them more active and prone to cause inflammation. Because an activated immune system is known to accelerate atherosclerosis, our findings could in part explain clinical observations of accelerated and aggressive forms of atherosclerosis among diabetic individuals. Therefore, the central focus of our grant proposal will be to uncover how hyperglycemia acts to alter microRNA levels in immune cells and their progenitors to drive their activation and thereby accelerate atherosclerosis. In our First Aim we will define which microRNA are altered in immune cells and their progenitors in the blood, spleen and atherosclerotic lesions of diabetic mice, and how this alters their cellular activation. We will study immune cells exposed to high levels of glucose to test if increased cellular oxidative stress is responsible for reducing microRNA levels. We will also identify which enzymes are responsible for these effects. In our Second Aim we will test if increasing an anti-oxidant activity in immune cells can overcome effects of hyperglycemia to maintain normal microRNA levels and thereby prevent immune cell activation and atherosclerosis in diabetic mice. We will also test if a forced expression of select microRNA in immune cells can overcome effects of hyperglycemia to reduce inflammation and atherosclerosis in diabetic mice. We will also test if these approaches can be combined with glucose lowering to control diabetic atherosclerosis. Our findings could provide much needed new treatments to diabetic individuals and those yet to develop diabetes based on the manipulation and use of microRNA to control diabetic atherosclerosis that remains a major cause of serious cardiovascular diseases despite widely available therapies that reduce blood glucose and lipids.

Public Health Relevance

Our focus is to determine why high blood sugar (also called hyperglycemia) causes immune cells to enhance the clogging of arteries with fatty deposits among diabetic individuals even after lowering their blood sugar. Using genetically engineered mouse models of atherosclerosis developed in our laboratory, we will investigate how hyperglycemia can alter the normal activity of immune cells by affecting the cellular expression of genetic regulatory molecules called microRNA. Our findings could lead to new therapeutic treatments based on microRNA to stop and even reverse fatty blockages and cardiovascular disease in diabetic individuals.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL133575-02
Application #
9276126
Study Section
Atherosclerosis and Inflammation of the Cardiovascular System Study Section (AICS)
Program Officer
Chen, Jue
Project Start
2016-06-01
Project End
2020-03-31
Budget Start
2017-04-01
Budget End
2018-03-31
Support Year
2
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Northern California Institute Research & Education
Department
Type
DUNS #
613338789
City
San Francisco
State
CA
Country
United States
Zip Code
94121