Rebecca L Holme

Children's Research Institute.; Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin 53226.

4 publications 2014 – 2017

What does Rebecca L Holme research?

Rebecca L Holme studies how specific harmful chemicals, especially those found in cigarette smoke, impact cholesterol levels and heart health. One of her primary focuses is on high-density lipoprotein (HDL), often referred to as 'good cholesterol.' HDL is critical for removing excess cholesterol from the body, but her research shows that exposure to certain toxins, like acrolein, can damage HDL, preventing it from functioning effectively. This damage can lead to harmful cholesterol buildup in cells, which can increase the risk of heart disease, particularly in smokers who might otherwise have normal HDL levels.

Key findings

  • Exposure to acrolein significantly damages HDL, hindering its ability to remove cholesterol from the body.
  • Damaged HDL can cause cholesterol to accumulate inside immune cells, rather than clearing it from the bloodstream.
  • Smokers, despite having HDL present, face a higher risk of heart disease due to the dysfunctional cholesterol transport caused by toxins.

Frequently asked questions

Does Dr. Holme study the effects of smoking on heart health?
Yes, she specifically researches how chemicals in cigarette smoke affect cholesterol and increase heart disease risk.
What treatments has Dr. Holme researched?
While her work primarily focuses on understanding the damage caused by smoking, it emphasizes the need for interventions that can protect or restore HDL function.
Is Dr. Holme's work relevant to patients with high cholesterol?
Yes, her findings provide insight into how smoking can worsen cholesterol levels and highlight the importance of protecting good cholesterol functions.

Publications in plain English

Domain Mapping of Heat Shock Protein 70 Reveals That Glutamic Acid 446 and Arginine 447 Are Critical for Regulating Superoxide Dismutase 2 Function.

2017

The Journal of biological chemistry

Afolayan AJ, Alexander M, Holme RL, Michalkiewicz T, Rana U +5 more

Plain English
This study examined how a protein called heat shock protein 70 (hsp70) interacts with another protein, superoxide dismutase 2 (SOD2), which helps protect cells from damage. Researchers found that specific parts of hsp70, particularly amino acids 446 and 447, are vital for this interaction and that when these amino acids were altered, the binding and function of SOD2 were negatively affected. Understanding this process is important because it can lead to new treatments that enhance SOD2's protective role in cells, which is crucial for combating oxidative stress-related diseases. Who this helps: Patients with conditions related to oxidative stress, like neurodegenerative diseases.

PubMed

Tryptophan 415 Is Critical for the Cholesterol Transport Functions of Scavenger Receptor BI.

2016

Biochemistry

Holme RL, Miller JJ, Nicholson K, Sahoo D

Plain English
This study looked at how a specific part of a protein called scavenger receptor BI (SR-BI) affects the transport of cholesterol in the body. Researchers found that when they removed a key piece known as Tryptophan 415, the SR-BI protein struggled to bind to cholesterol-carrying particles and could not effectively remove cholesterol from cells. This is important because understanding how cholesterol is transported can help in developing treatments for diseases linked to cholesterol levels, like heart disease. Who this helps: This helps doctors and researchers developing treatments for patients with high cholesterol and related heart conditions.

PubMed

Acrolein impairs the cholesterol transport functions of high density lipoproteins.

2015

PloS one

Chadwick AC, Holme RL, Chen Y, Thomas MJ, Sorci-Thomas MG +3 more

Plain English
Researchers exposed HDL (the "good cholesterol" that normally protects against heart disease) to acrolein, a toxic chemical in cigarette smoke, and found that it damaged the HDL and made it unable to do its job of removing cholesterol from the body. The damaged HDL not only failed to pick up cholesterol from cells but actually caused cholesterol to accumulate inside immune cells instead of being removed. This means smoking damages your good cholesterol so badly that it works backwards—it helps cholesterol build up in your arteries rather than clearing it out, which could explain why smokers have higher heart disease risk despite having HDL in their blood.

PubMed

SR-BI/CD36 chimeric receptors define extracellular subdomains of SR-BI critical for cholesterol transport.

2014

Biochemistry

Kartz GA, Holme RL, Nicholson K, Sahoo D

Plain English
This study looked at a protein called SR-BI that helps move cholesterol from the body to the liver using a process involving high-density lipoproteins (HDLs). Researchers created altered versions of SR-BI to understand which parts of the protein are necessary for effective cholesterol transport. They found that certain areas of SR-BI are crucial for its ability to bind to HDLs and deliver cholesterol; most of the altered proteins performed worse in these tasks, showing a significant drop in their cholesterol transport function. Who this helps: This research benefits patients at risk for cardiovascular disease by enhancing understanding of cholesterol transport mechanisms.

PubMed

Publication data sourced from PubMed . Plain-English summaries generated by AI. Not medical advice.