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Your Environment. Your Health.

AMBIENT FINE PARTICULATE MATTER AND BONE MARROW STEM CELLS

Export to Word (http://www.niehs.nih.gov//portfolio/index.cfm/portfolio/grantdetail/grant_number/R01ES026200/format/word)
Principal Investigator: Liu, Zhenguo
Institute Receiving Award University Of Missouri-Columbia
Location Columbia, MO
Grant Number R01ES026200
Funding Organization National Institute of Environmental Health Sciences
Award Funding Period 01 Sep 2016 to 31 Aug 2021
DESCRIPTION (provided by applicant):  : Ambient fine particulate matter (PM) is the key components for air pollution, and associated with significant mortality. The majority of the mortality following PM exposure is related to cardiovascular diseases. Endothelial progenitor cells (EPCs) are critical to maintaining the integrity and function of blood vessels with bone marrow as one of their main sources. PM exposure exhibits various deleterious effects on cardiovascular system, and significantly decreases the number and function of EPCs. However, the mechanism(s) for PM exposure- induced impairment of EPCs has not been fully understood. Recently, we observed that PM exposure significantly decreased the level of circulating EPCs s and the population of bone marrow stem cells (BMSCs) within the bone marrow in association with increased level of reactive oxygen species (ROS) formation in mice. When ROS production was blocked, PM-induced reduction of EPCs and BMSCs was effectively prevented. The present project was proposed to test the hypothesis that "PM exposure reduces the number and function of EPCs through oxidative stress-mediated reduction of BMSC population in bone marrow with reduced generation of EPCs from BMSCs". There are two specific aims: 1): to determine the effect of PM exposure on BMSCs and their endothelial differentiation; and 2): to define the role of oxidative stress in mediating the effect of PM exposure on BMSCs and their differentiation into EPCs. We will demonstrate that PM exposure leads to a significant reduction in the number and function of BMSCs in the bone marrow. We will determine if the decrease in the number of BMSCs is due to increased apoptosis or decreased proliferation. We will also conduct experiments using bone marrow transplantation (BMT) with eGFP-positive BMSCs to determine if PM exposure impairs the differentiation of BMScs into EPCs that may contribute to decreased number and function of EPCs in the setting of PM exposure. To determine if PM exposure could produce a similar effect on BMSCs as chronic air pollution, the experiments will be repeated using mice exposed to air pollution for up to 6 months. We will test whether PM-induced ROS production causes decreased number and function of BMSCs by blocking ROS production using either antioxidant N-acetylcysteine or concomitant overexpression of an antioxidant enzyme network of human copper/zinc superoxide dismutase (SOD) 1, extracellular SOD3, and glutathione peroxidase with decreased ROS formation. We will also use BMT model with eGFP-BMSCs to determine if PM-induced oxidative stress plays a critical role in the differentiation of BMSCs into EPCs. Experiments will be conducted to evaluate the role of ROS in the population of BMSCs and their differentiation into EPCs in the mice exposed to air pollution for up to 6 months. The data from this study will provide important and novel information on the mechanisms for the development of cardiovascular diseases in patients with PM exposure and air pollution, and help explore new approaches to preventing and treating cardiovascular diseases related to PM exposure. 1
Science Code(s)/Area of Science(s) Primary: 17 - Stem Cell Biology and Cellular Differentiation
Publications See publications associated with this Grant.
Program Officer Leslie Reinlib
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