Showing posts with label WBCs. Show all posts
Showing posts with label WBCs. Show all posts

Sunday, June 12, 2016

Alzheimer's Fighting off Infections; Who Knew?

 
INTRODUCTION:
Recent research indicates that Alzheimer's can stem from the toxic remnants of the brain's attempt to fight off infections. Team of researchers from Harvard are close to finding the reason behind the origins of plaque tau found in individuals who suffer from Alzheimer's.

Experts on Alzheimer's disease are captivated by the idea that infections, those that are too mild to cause actual symptoms could possibly produce a fierce reaction leaving debris in the brain and in this case causing Alzheimer's in people as they age. The hypothesis makes sense and the data supports the hypothesis in that the major implications for preventing and treating this degenerative brain disease.
Dr. Michael W. Weiner is a radiology professor at University of California, San Francisco. He is the lead investigator of the Alzheimer’s Disease Neuroimaging Initiative where the goal of the organization is to create a large national effort to track the progression of the disease and look for biomarkers like blood proteins and brain imaging to signal the disease’s presence.

A virus, fungus, or a bacterium gets into the brain, passing through the the blood brain barrier membrane which becomes leakier with age. The brain’s defense system rushes in to stop the invader by making a sticky cage out of proteins, called beta amyloid. The microbe gets trapped, leaving behind a plaque that is the unique hallmark of Alzheimer’s. Data from the research, so far, have supported their hypothesis of the neurons growing in petri dishes including those in yeast, roundworms, fruit flies, and mice.
 
 
The origins of this idea and its work started with Robert Moir who had an idea about the function of amyloid proteins, normal brain proteins which have always been a mystery. The hypothesis has been that with age the brain accumulates 'garbage' that were called proteins by scientists. What Dr. Moir noticed that others didn't was that the proteins looked very similar to that of the innate immune system. What does this mean? The innate immune system is a primitive system that is the body's first line of defense against infections.

If these proteins were to be found anywhere else in the body, for example proteins called trap microbes ( viruses, fungi, yeast, bacteria). After the initial defense, the body releases WBCs to clear up any mess formed. Dr. Moir, came to the conclusion of the possibility that amyloids were also part of that system. AT Harvard Medical School and Massachusetts' General hospital, he began working with Rudolph Tanzi on a study to see if amyloids were trapped in microbes in living animals as well as if mice which lack these amyloid proteins were quickly ravaged by infections that amyloid could have stopped.
In a study where salmonella was injected in the bacteria in the brains of young mice that did not have plaques. Overnight, the bacteria gave birth to plaques. The hippocampus was full of plaques, and each plaque had a single bacterium at its center. Those that did not form beta amyloid plaques succumbed more quickly to the bacterial infection. Plaques never formed in their brains.

The idea in researchers minds has always been that the plaques were a form of trash accumulated in the brain. Alzheimer's pathway is supported by years of research. Plaques form and set off the formation of  tangled threadlike tau proteins. Then, as tangles of tau kill nerve cells, the brain becomes inflamed, resulting in the killing of many more nerve cells. There were a few puzzling clues that something else might be going on, but they did not make much sense.
Investigators have indeed reported that individuals who developed Alzheimer’s revealed to have higher levels of antibodies to herpes- an indication of a previous infection- compared to those who did not have the disease. Dr. Berislay Zlokovic's studies also support this statement. The blood brain barrier fits this hypothesis. He discovered that the barrier began degrading due after years of aging and of all the regions, the hippocampus (site of learning and memory) was the leakiest part of the membrane. Coincidentally, this is also where Alzheimer’s plaques form.
 
 
Then there are individuals who have a mutated gene that guarantees that they will eventually develop the disease at an early age. The problem here is that these individuals vastly overproduce beta amyloid. So much of these begin to clump up even without the presence of microbes. Uniquely enough, not everyone who has had a brain infection develops Alzheimers. Some individuals seem to be more vulnerable to the disease than others.
A new theory proposes that the brain has the ability to clear out balls of beta amyloid after they have killed the microbes. Individuals with the gene 'ApoE2' have brains that are skilled at clearing out this plaque subsequently lowering their risk of developing Alzheimer's in their later years. Then there are individuals who have different version of this gene which are inefficient in removing plaque and therefore have a high risk of developing Alzheimer's.

The incidence of dementia has been declining is the past few years. The reasoning behind the results of these recent data suggests that individuals have been taking better control of their blood pressures and cholesterol levels. By doing so, they are starving off mini strokes which can cause dementia. Much more work is needed in this area of medical research.
 
 
 
The Cure Alzheimer’s Fund is initiating a large collaborative project that will use gene sequencing technology to carefully look for microbes in the brain. These careful observations will range from the brains of people who had Alzheimer's and those who never developed the disease. The microbes located within the plaques in human brains will also be collected. Dr. Tanzi strongly suggests that the very first question that needs to be answered is whether there are microbes that can sneak into the brain as we age triggering amyloid deposition so that we can then set a new goal in stopping them.
Links:
(A)http://www.nytimes.com/2016/05/26/health/alzheimers-disease-infection.html?_r=0

*Please note! These images are not mine. They were found on various tumblr sites! If any are yours please let me know so that I can give you credit for them! Also the people in the images have no relation to the diseases, illnesses, or cancers I write about. Thanks so much & enjoy~

Tuesday, October 27, 2015

Man Made Blood

According to British authorities, 'man-made blood' will be available to be transfused into humans in the next two years. Research assistant director, Dr. Nicholas Watkins, who specializes in NHS blood and transplant research and development states that the intention behind such research is to offer specific patient groups special treatment according to their disease, illness, etc. It is NOT for the intention to replace human donation. Scientists across the globe have been investigating for a number of years how to manufacture red blood cells to offer an alternative to donated blood to treat patients," he said. "We are confident that by 2017 our team will be ready to carry out the first early phase clinical trials in human volunteers. These trials will compare manufactured cells with donated blood. Continued investment in research and development is critical to our role in saving and improving lives through blood and organ donation." (A)

Scary Decline in Blood Donations:
Quiet recently, a warning of the evolving crisis of blood donation along with the huge decline of volunteers offering to donate blood according to NHS authorities. Figures show that there have been  40% fewer donors that came from England and Wales between the years of 2014 and 2015 compared to the years 2004 and 2005. This dramatic decline has been blamed on individuals with excessive tattoos and exotic holidays that do not permit these individuals to donate. (A)There needs to be an increase of 70% or 204,000 new blood donors to ensure that the nation's blood stocks are at a 'safe' or 'secure' level. Other reasons as to why such a dramatic decline in blood donors is because people are too busy and exotic travel which eliminates many candidates for donation in the short-term. (A)

Research Conducted:
Blood making or hematopoietic stem cells give birth to every cell circulating in your blood system whether they are RBCs, WBCs, or platelets. These stem cells contain within them the secret to stress, old age, and disease. The fates of these unspecialized cells occur in the bone marrow and shape blood production. The bone marrow is where the hematopoietic stem cells decide what type of blood cells need to be made before being released into circulation. (B)

Emmanuelle Passegué's work on rejuvination and longer life span stems from her passion of studying blood. Eager to find out through her research how we age and our body's response to diseases. Her primary goal is to develop effective remedies for blood diseases such as leukemia, lymphoma, bone marrow failures, and anemia. 

Recently, her interest in blood and her focus soon became 'how aging affects hematopoietic stem cells'. There are only a certain number of hematopoietic stem cells that we are born with and because these stem cells age with us, there will be only a few remaining hematopoietic stem cells that will still function properly. Subsequently, this leaves our bodies increasingly vulnerable to various infections, blood diseases, and fatal illnesses.(B)

 In their paper, Cell Stem Cell', Passegue and her UCSF lab team described that if the causes of the decline in functionality which is heavy age-related can be understood, then the possibility to rejuvenate the older stem cells so that the health of the entire blood system can be maintained then the possibility of a longer life is possible. (B)

Other researchers, besides Passque and her UCSF lab team, are investigating the use of adult stem cells and blood from umbilical cord as alternatives for blood donation, specifically those with complex blood types who have a difficult time finding compatible donors so that the body does not reject the donation. (A) 

Biomedical engineers from the human bone marrow have produced functional blood platelets, also known as the cells within our circulatory system that causes clots to form, within the lab. This first step, is bringing researchers and scientists closer to man-made blood transfusions. This type of transfusion has only been tested on lab mice. The NHS Blood and Transport is one of eight goals of the 2020 Research and Development program that aims to develop transfusion, transplantation and regenerative medicine over the next five years. (A) Recent research program lead by Bristol, Cambridge, and Oxford Universities, are dedicated to patients with sickle cell anemia and thalassemia who need regular blood transfusions with their treatments. (A)

Links:
(A)http://www.telegraph.co.uk/news/nhs/11697294/Blood-made-in-the-lab-will-be-given-to-humans-in-two-years.html
(B)https://www.ucsf.edu/news/2015/08/131406/emmanuelle-passegue-making-better-blood

*These images do not belong to me- they were found on various tumblr sites! If any are yours please let me know and I will give you credit for them! Thanks so much!*