Why do brain cells die after a stroke?

Biology
Open Access
$80
Raised of $2,500 Goal
4%
Ended on 8/29/13
Campaign Ended
  • $80
    pledged
  • 4%
    funded
  • Finished
    on 8/29/13

About This Project

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What is the context of this research?

The goal of this project is to examine the role of a protein, CaMKII, in the cell death pathway that is activated following stroke. Massive cell death that occurs following a stroke is responsible for all of the detrimental effects that are associated with stroke (i.e. motor function impairments, cognitive decline, etc.)

For the most part, strokes are caused by a blood vessel blockage or rupture that stops blood flow to part of the brain. The brain cells at the core of a stroke usually end up dying and can't be saved. When these cells are dying, they release many of their contents which kills surrounding cells in what is called secondary cell death. In addition to this toxic release, a prolonged inflammation response causes further damage brain cells.

We know it is possible to decrease the amount of secondary death, and thus decrease the effects of the stroke, but the cellular pathways that cause this death are not completely understood. By examining a model of stroke in cultured brain cells, I hope to further our understanding of stroke in order to protect ourselves from the cascading effects which cause so much additional damage.

What is the significance of this project?

Stroke is the leading cause of disability worldwide. Nearly everyone is or will be affected by stroke. Surprisingly, there is currently only one approved drug treatment for patients who have suffered from a stroke, and its effectiveness is very limited. Many additional drug treatments have made it to clinical trials but have failed to reproduce the promising results seen in rodent studies.

This research is important because it aims to look at cellular mechanisms beyond what are currently targeted in clinical trials.

Examining changes in CaMKII that result following excitotoxicity and inflammatory responses may help identify mechanisms involved in stroke-related cell death and eventually determine new target pathways for stroke intervention. This is important because stopping cell death could mean the difference between minor cognitive impairments or major loss of function.

What are the goals of the project?

Fortunately, the laboratory I work in currently has enough funding to finance most of what is required for the experiments I have proposed. However, there is not enough funding to support me as a research assistant.

Securing this funding will provide a modest stipend which will make the difference between me being able to conduct these experiments this summer/fall or having to find a job elsewhere and put these experiments on hold. In addition, about $500 (of the $2500) will go towards a few additional and essential reagents for this specific project.

Working in the laboratory this summer is my goal and will be made entirely possible with help from Microryza donors like you. If you have any questions about me or my experiments before donating, please don’t hesitate to contact me!

Email: braggr@students.wwu.edu

Budget

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A large bulk of my budget will be for a stipend to support me financially while I conduct this research ($1000/month, for two months)

The cost of culturing cells is covered by my professor’s laboratory, including almost all of the necessary components to run these experiments (antibodies, reagents, etc.).

CXCL12 is a signaling molecule that becomes upregulated following stroke. I will be applying it to cultured neurons to mimic the conditions that may occur following a stroke ($250).

Calcium sensitive dye is a dye that changes color in the presence of calcium. I will be using it to visualize the intracellular spike of calcium that is known to occur so that I can correlate it with the activation of proteins, including CaMKII ($250).

Meet the Team

Robert Bragg
Robert Bragg

Affiliates

Master of Science student, Western Washington University
BA Psychology, Western Washington University (2012)
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Team Bio

I am currently a Master’s student at Western Washington University. I am working under the advisement of Dr. Jackie Rose. Her laboratory utilizes primary cell culture of hippocampal neurons to study molecular dynamics of various phenomena including learning, memory, and excitotoxicity. I am still in the early stages of my research career, which makes it crucial for me to get funding from new alternative sources, such as Microryza. Small grants, like the one’s here, really go a long way for young scientists like me.

Robert Bragg

I am currently a Master’s student at Western Washington University. I am working under the advisement of Dr. Jackie Rose. Her laboratory utilizes primary cell culture of hippocampal neurons to study molecular dynamics of various phenomena including learning, memory, and excitotoxicity. I am still in the early stages of my research career, which makes it crucial for me to get funding from new alternative sources, such as Microryza. Small grants, like the one’s here, really go a long way for young scientists like me.

Lab Notes

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Project Backers

  • 3Backers
  • 4%Funded
  • $80Total Donations
  • $26.67Average Donation
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