Articles to be published in the May 2007 issue of the Journal of Lipid Research (Vol. 48, No. 5)
Fish, Seafood Better than Olive Oil, Nuts against Heart Disease
Researchers have found that a diet rich in fish, seafood, and grains – also called polyunsaturated fats – is better at preventing heart disease than a diet containing olive oil, nuts, and avocados – called monounsaturated fats. Although both types of fats are healthy, people should probably include more of the first than the second in their diet to keep a healthy heart, the scientists say.
Too much cholesterol has long been linked to increasing risks of developing heart disease, but it has been less clear how the various dietary fats – saturated, monounsaturated and polyunsaturated – make people susceptible to the disease.
Lawrence L. Rudel and colleagues developed a method to determine the effects of the three types of dietary fats on acyl-coenzyme A, a key molecule involved in the metabolism of fatty acids. The scientists found that mice fed diets high in saturated and monounsaturated fat showed an increase in acyl-coenzyme A compared to mice fed a diet enriched in polyunsaturated fat. These results suggest that polyunsaturated fat is a more suitable replacement than monounsaturated fat for dietary saturated fat, the scientists concluded.
Article: "Monounsaturated fatty acyl-CoA is predictive of atherosclerosis in human ApoB100 transgenic, LDLr-/- mice" by Thomas A. Bell III, Martha D. Wilson, Kathryn Kelley, Janet K. Sawyer, and Lawrence L. Rudel
MEDIA CONTACT: Lawrence L. Rudel, Department of Pathology and Lipid Sciences, Wake Forest University School of Medicine, Winston-Salem, N.C.; e-mail: email@example.com
Heart Disease Linked to Too Much Cholesterol in Cell Organelle
Scientists have shown that a build-up of cholesterol in cell organelles called lysosomes is related to a higher incidence of heart disease.
Atherosclerosis, a heart disease in which fat accumulates in arteries and blocks blood flow, is the leading cause of death in the Western World. One hallmark of the disease is the presence of cells called macrophage foam cells, in which cholesterol accumulates. Scientists are now trying to understand how cholesterol builds up in these cells, especially in cellular organelles called lysosomes that are known for degrading cholesterol.
W. Gray Jerome and colleagues noticed that when cholesterol accumulates in lysosomes, they become less acidic, which makes them less active. The lysosomes become unable to degrade all the cholesterol that comes in, and more cholesterol accumulates over time. These observations suggest that restoring the acidity of lysosomes may be a promising way to clear up arteries from cholesterol and to potentially prevent heart disease.
Article: "Effects of Cellular Cholesterol Loading on Macrophage Foam Cell Lysosome Acidification" by Brian E. Cox, Evelyn Griffin, Jody C. Ullery, and W. Gray Jerome
MEDIA CONTACT: W. Gray Jerome, Department of Pathology, Vanderbilt University Medical Center, Nashville, Tenn.; tel.: 615-322-5530; e-mail: firstname.lastname@example.org
New Link Between Down Syndrome and Alzheimer's Disease
Scientists have shown that a protein involved in cholesterol metabolism may cause the accelerated onset of Alzheimer's Disease in individuals affected with Down Syndrome.
People with Down Syndrome – a genetic disorder due to the presence of an extra chromosome 21 – develop Alzheimer's disease (AD) earlier (mid- to late 30s) than the general population (mid- to late 70s). To understand why, scientists have studied genes from chromosome 21 that are also involved in AD. One of those genes has already been found: It produces a protein called amyloid precursor protein (APP) that helps create protein clusters that are the hallmark of AD.
Cheryl L. Wellington and colleagues have found another gene on chromosome 21 that produces a protein that regulates the amount of cholesterol present in a cell. The scientists showed that this protein influences the distribution and processing of APP and that it is present at high levels in the brains of Down Syndrome individuals. The new discovery may provide new ways to halt AD symptoms early in these individuals.
Article: "The cholesterol transporter ABCG1 modulates the subcellular distribution and proteolytic processing of beta-amyloid precursor protein" by Gavin H. Tansley, Braydon L. Burgess, Matt T. Bryan, Yuan Su, Veronica Hirsch-Reinshagen, Jonathan Pearce, Jeniffer Y Chan, Anna Wilkinson, Jeanette Evans, Kathryn E. Naus, Sean McIsaac, Kelley Bromley, Weihong Song, Hsui-Chiung Yang, Nan Wang, Ronald B. DeMattos, and Cheryl L. Wellington
MEDIA CONTACT: Cheryl L. Wellington, University of British Columbia, Vancouver, Canada; e-mail: email@example.com
The following article is the last in a series of nine reviews on "lipid post-translational modification" or how lipids are added to proteins after they are produced in the cell. The other articles in the series appeared in previous issues of the journal.
All thematic review articles and can be accessed at: http://www.jlr.org/ (under "Thematic Reviews").
How Lipids Anchor Proteins on a Cell Membrane
Peter Orlean and Anant K. Menon describe how a lipid that helps proteins attach to cell membranes is made. The protein, called glycosylphosphatidylinositol (GPI), is important because people with defective GPI can develop seizures, have heart attacks, and acquire a hemolytic condition in which red blood cells are destroyed. Also, elevated levels of certain proteins involved in GPI anchoring have been linked to breast and bladder cancers.
GPI synthesis is initiated on the cytoplasmic side of the membrane of the endoplasmic reticulum (ER), then the resulting precursor molecule flips inside the ER, where further molecules are progressively added to it to form the complete GPI. The GPI is then linked to a protein, and the lipid-modified protein then leaves the ER for the cell membrane, where it is anchored on the outer side of the membrane via its GPI.
Orlean and Menon review the latest findings on GPI assembly in the ER, its transfer to a protein, and the changes made to GPI on its way to the cell membrane. They describe the enzymes and chemical reactions involved and highlight questions that need to be addressed, especially how GPI structure affects the proteins they carry with them and how the various components of the GPI anchoring machinery work together. Answering these questions would not only help better understand GPI assembly, but could also lead to new drugs against diseases associated with defective GPI.
Article: GPI anchoring of protein in yeast and mammalian cells or: How we learned to stop worrying and love glycophospholipids" by Peter Orlean and Anant K. Menon
MEDIA CONTACT: Anant K. Menon, Department of Biochemistry, Weill Cornell Medical College, New York; e-mail: firstname.lastname@example.org
MEDIA CONTACT: Peter Orlean, Department of Microbiology, University of Illinois at Urbana-Champaign, Urbana; e-mail: email@example.com
MEDIA CONTACT: Stephen G. Young, Coordinator of the Thematic Review Series on Lipid Post-translational Modification, Department of Internal Medicine, University of California, Los Angeles, CA; e-mail: firstname.lastname@example.org
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