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Showing posts with label Protein. Show all posts
Showing posts with label Protein. Show all posts

Sunday, January 6, 2013

Researchers Identify Role For Protein Linked To Obesity, Type 2 Diabetes

Main Category: Diabetes
Also Included In: Obesity / Weight Loss / Fitness;  Biology / Biochemistry
Article Date: 21 Dec 2012 - 0:00 PST Current ratings for:
Researchers Identify Role For Protein Linked To Obesity, Type 2 Diabetes
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Researchers at UT Southwestern Medical Center have taken another step toward better understanding the metabolic functions of obesity and its connection to type 2 diabetes.

Dr. Philipp Scherer, Director of the Touchstone Center for Diabetes Research at UT Southwestern, led a group of researchers in a recent multicenter study published in Nature Medicine that successfully identified ways to manipulate the protein mitoNEET. This is the first time the protein has been effectively altered to expand fat tissue in a way that allows subjects - in this case, mice - to remain metabolically healthy.

MitoNEET is a key component of a cell's mitochondrion, which serves as the cell's energy powerhouse. When the levels of MitoNEET protein were elevated inside the fat cells of rodents, more fat was stored in the adipose tissue, thereby keeping toxic lipids away from other types of cells. This sequestration resulted in extremely obese yet metabolically healthy mice that displayed no signs of type 2 diabetes. In contrast, when MitoNEET levels were decreased, the mice became lean but unhealthy, and developed pre-diabetic conditions such as failure to metabolize glucose properly.

"The manipulation of mitochondrial activity in fat tissue is a very powerful approach to control how much excess energy we store in our bodies and where we store it. We have heretofore underestimated the importance of mitochondrial pathways in our fat cells and their influence on how we manage our weight," said Dr. Scherer, senior author of the three-year study and Professor of Internal Medicine and Cell Biology at UTSW.

The body stores fat in the white adipose tissue, and, ideally, individuals burn any excess calories through exercise and a healthy diet. The current research findings suggest that manipulating components of mitochondria in fat cells can be an effective way to funnel excess calories into "good" locations. This storage then thwarts their negative effect on other internal organs like the liver in which excess fat accumulation is toxic.

The obese mice in this study weighed 120 to 130 grams (4.23 to 4.58 ounces), whereas a normal adult mouse weighs 25 to 30 grams (.88 to 1.06 ounces). This difference is the equivalent of a 150-pound person increasing his or her weight to 700 pounds.

The researchers were careful to clarify that the findings were not meant to encourage obesity, even though the obese mice were considered metabolically healthy. The study instead provides a clearer understanding of the mitochondrion's importance to the metabolic dysfunction - that is characteristic of obese patients and those with type 2 diabetes.

"These results taught us a great deal about how fat cells sense, store, and burn energy," said Dr. Christine Kusminski, a postdoctoral researcher in Internal Medicine who served as the study's first author. "By learning more about the underlying mechanisms, we hope to develop ways to target these pathways for future drug development."

The researchers now hope to translate these findings into a clinical setting. The staff of the Touchstone Center is devoted to the study of cells and tissues that either contribute to or are affected by diabetes and related diseases, including the physiology of adipose tissue.

Other UT Southwestern researchers involved in the study were Dr. William L. Holland, Instructor in Internal Medicine; Dr. Kai Sun, Assistant Instructor in Internal Medicine; Dr. Jiyoung Park, Assistant Instructor in Internal Medicine; and Stephen B. Spurgin, a medical student. Scientists from the Albert Einstein College of Medicine, the University of Utah School of Medicine, and Merck Research Laboratories also contributed.

The investigation was funded by support from the National Institutes of Health, the American Heart Association, and fellowships from the Juvenile Diabetes Research Foundation and the Department of Defense.

Article adapted by Medical News Today from original press release. Click 'references' tab above for source.
Visit our diabetes section for the latest news on this subject. Please use one of the following formats to cite this article in your essay, paper or report:

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Wednesday, July 18, 2012

New Treatment Directions Suggested By Alzheimer's Protein Structure

Main Category: Alzheimer's / Dementia
Also Included In: Cholesterol
Article Date: 02 Jun 2012 - 0:00 PDT Current ratings for:
'New Treatment Directions Suggested By Alzheimer's Protein Structure'
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The molecular structure of a protein involved in Alzheimer's disease - and the surprising discovery that it binds cholesterol - could lead to new therapeutics for the disease, Vanderbilt University investigators report in the June 1 issue of the journal Science.

Charles Sanders, Ph.D., professor of Biochemistry, and colleagues in the Center for Structural Biology determined the structure of part of the amyloid precursor protein (APP) - the source of amyloid-beta, which is believed to trigger Alzheimer's disease. Amyloid-beta clumps together into oligomers that kill neurons, causing dementia and memory loss. The amyloid-beta oligomers eventually form plaques in the brain - one of the hallmarks of the disease.

"Anything that lowers amyloid-beta production should help prevent, or possibly treat, Alzheimer's disease," Sanders said.

Amyloid-beta production requires two "cuts" of the APP protein. The first cut, by the enzyme beta-secretase, generates the C99 protein, which is then cut by gamma-secretase to release amyloid-beta. The Vanderbilt researchers used nuclear magnetic resonance and electron paragmagnetic resonance spectroscopy to determine the structure of C99, which has one membrane-spanning region.

They were surprised to discover what appeared to be a "binding" domain in the protein. Based on previously reported evidence that cholesterol promotes Alzheimer's disease, they suspected that cholesterol might be the binding partner. The researchers used a model membrane system called "bicelles" (that Sanders developed as a postdoctoral fellow) to demonstrate that C99 binds cholesterol.

"It has long been thought that cholesterol somehow promotes Alzheimer's disease, but the mechanisms haven't been clear," Sanders said. "Cholesterol binding to APP and its C99 fragment is probably one of the ways it makes the disease more likely."

Sanders and his team propose that cholesterol binding moves APP to special regions of the cell membrane called "lipid rafts," which contain "cliques of molecules that like to hang out together," he said.

Beta- and gamma-secretase are part of the lipid raft clique.

"We think that when APP doesn't have cholesterol around, it doesn't care what part of the membrane it's in," Sanders said. "But when it binds cholesterol, that drives it to lipid rafts, where these 'bad' secretases are waiting to clip it and produce amyloid-beta."

The findings suggest a new therapeutic strategy to reduce amyloid-beta production, he said.

"If you could develop a drug that blocks cholesterol from binding to APP, then you would keep the protein from going to lipid rafts. Instead it would be cleaved by alpha-secretase - a 'good' secretase that isn't in rafts and doesn't generate amyloid-beta."

Drugs that inhibit beta- or gamma-secretase - to directly limit amyloid-beta production - have been developed and tested, but they have toxic side effects. A drug that blocks cholesterol binding to APP may be more specific and effective in reducing amyloid-beta levels and in preventing, or treating, Alzheimer's disease.

The C99 structure had some other interesting details, Sanders said.

The membrane domain of C99 is curved, which was unexpected but fits perfectly into the predicted active site of gamma-secretase. Also, a certain sequence of amino acids (GXXXG) that usually promotes membrane protein dimerization (two of the same proteins interacting with each other) turned out to be central to the cholesterol-binding domain. This is a completely new function for GXXXG motifs, Sanders said.

"This revealing new information on the structure of the amyloid precursor protein and its interaction with cholesterol is a perfect example of the power of team science," said Janna Wehrle, Ph.D., who oversees grants focused on the biophysical properties of proteins at the National Institutes of Health's National Institute of General Medical Sciences (NIGMS), which partially funded the work. "The researchers at Vanderbilt brought together biological and medical insight, cutting-edge physical techniques and powerful instruments, each providing a valuable tool for piecing together the puzzle."

Sanders is proud that the studies reflect the value of basic science research and the full continuum of basic to clinical science.

"When we were developing bicelles 20 years ago, no one was saying, 'someday these things are going to lead to discoveries in Alzheimer's disease,'" he said. "It was interesting basic science research that is now paying off."

Article adapted by Medical News Today from original press release. Click 'references' tab above for source.
Visit our alzheimer's / dementia section for the latest news on this subject. The Vanderbilt team included lead authors Paul Barrett and Yuanli Song, Ph.D., as well as Wade Van Horn, Ph.D., Eric Hustedt, Ph.D., Johanna Schafer, Arina Hadziselimovic and Andrew Beel.
The research was supported by grants from NIGMS (GM080513) and the Alzheimer's Association.
Vanderbilt University Medical Center Please use one of the following formats to cite this article in your essay, paper or report:

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7 Jun. 2012. APA

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Thursday, July 5, 2012

Risk Of Blood-Vessel Constriction Linked To Gum Disease May Be Increased By Specific Protein

Main Category: Dentistry
Also Included In: Cholesterol
Article Date: 20 Apr 2012 - 0:00 PDT Current ratings for:
'Risk Of Blood-Vessel Constriction Linked To Gum Disease May Be Increased By Specific Protein'
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A protein involved in cellular inflammation may increase the risk of plaque containing blood vessels associated with inflammatory gum disease, according to research presented at the American Heart Association's Arteriosclerosis, Thrombosis and Vascular Biology 2012 Scientific Sessions in Chicago.

The protein, CD36, is found in blood cells, as well as many other cell types. Research has shown that CD36 may increase the harmful effects of "bad cholesterol," or low-density lipoprotein (LDL).

Investigators "knocked out," or deleted, the gene responsible for CD36 production, then induced plaque in blood vessels by feeding mice a high fat diet. Some animals were also infected with the bacteria associated with gum disease.

More fatty plaque accumulation occurred in the blood vessels of the animals that were infected with gum disease. In the animals with the deleted CD36 gene, however, vessels remained free of new plaque even when oral inflammation occurred.

Article adapted by Medical News Today from original press release. Click 'references' tab above for source.
Visit our dentistry section for the latest news on this subject. Please use one of the following formats to cite this article in your essay, paper or report:

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American Heart Association. "Risk Of Blood-Vessel Constriction Linked To Gum Disease May Be Increased By Specific Protein." Medical News Today. MediLexicon, Intl., 20 Apr. 2012. Web.
7 Jun. 2012. APA

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'Risk Of Blood-Vessel Constriction Linked To Gum Disease May Be Increased By Specific Protein'

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View the original article here