Online friends
Search Articles
Tag Cloud
- depression
- intro
- anxiety
- piracetam
- supplements
- nootropic
- aging
- longevity
- Hello
- noopept
- Dopamine
- modafinil
- brain
- c60
- cancer
- ADHD
- resveratrol
- 07-04-2015
- stack
- health
- choline
- 01-04-2015
- memory
- new
- Aniracetam
- nad+
- nmn
- sleep
- introduction
- diet
- brain fog
- Exercise
- mitochondria
- ----
- anhedonia
- life extension
- rapamycin
- pramiracetam
- oxiracetam
- phenibut
- serotonin
- Supplement
- GABA
- stem cells
- cryonics
- research
- brain health
- ssri
- alcar
- nootropics
Fight Aging News
-
Quantifying the Distance in Years Between Healthspan and Lifespan
That medical science has been able to slightly co...
Yesterday, 07:20 PM Read Full Story -
Towards Regeneration of Aged Neuromuscular Junctions
The neuromuscular junction is a small, complex st...
Yesterday, 11:22 AM Read Full Story -
More Evidence for a Dysfunctional Gut Microbiome in Alzheimer's Disease
A growing body of evidence correlates an altered...
Yesterday, 11:06 AM Read Full Story -
Cellular Senescence as a Contributing Cause of Secondary Harms Following Stroke
Stroke is the blockage or rupture of a blood vess...
Dec 24 2024 06:55 PM Read Full Story -
Circadian Rhythm and the Inflammasome
The research noted here, showing that innate immu...
Dec 24 2024 11:22 AM Read Full Story -
FOXO3 is Involved in Elimination of Unfit Cells via Cell Competition
Early multicellular organisms must have fairly qu...
Dec 24 2024 11:11 AM Read Full Story
LongeCity Research Support 2013: Mitochondrial Gene Therapy
After careful consideration of a very competitive round this year, we are delighted to have identified a research team and project that we can warmly recommend for community funding:
DEVELOPMENT OF AN INNOVATIVE GENE THERAPY METHOD TO CURE MITOCHONDRIAL AGING-
"BACKING UP" THE MITOCHONDRIAL GENOME
Background:
Mitochondria, the power plants of the cell, contain their own DNA. Unlike the nucleus, mitochondria lack an efficient system to repair damaged DNA, and this damage accumulates over time. As we age, these accumulated mutations result in an increase in oxidative stress throughout the body. It is no coincidence that organisms which age more slowly consistently display lower rates of mitochondrial free radical damage. Reversing and/or preventing damage to mitochondrial DNA may be a key factor in slowing the aging process.
The Research Project:
In this project, engineered mitochondrial genes will be used to restore function to cells that contain defective mitochondrial genes.
The SENS team is developing a unique method for targeting these genes to the mitochondria; this step has been the bottleneck in research on this topic over the last decade. In their system, the mRNA from the engineered mitochondrial gene is targeted to the mitochondrial surface before it is translated into a protein using a co-translation import strategy. Once imported, it is incorporated into the correct location in the inner mitochondrial membrane. The long-term goal of this project is to utilize this improved targeting strategy to rescue mutated mitochondrial DNA and thereby prevent and cure one of the major causes of cellular aging.
The Team:
Dr. Matthew 'Oki' O'Connor former Post-Doctoral Scholar at the Bioengineering Department University of California Berkeley (PI: Irina M. Conboy) is now a Senior Researcher at the SENS Research Foundation Research Center in Mountain View, California
--
--the team --the lab
Research brief here:
View attachment: LCSci2013_3.pdf
Or here
You can pose questions to the researcher here.
CLICK TO DONATE
8 Comments
Please email treasurer@longecity.org.
Contribute today for the greatest 'bang for your buck' effect in supporting anti-aging research you can find this year!
All donations are trebled!
View the full article
In case you were not counting, our organization still has a 100% success rate of funding life extension research. Every fundraising goal for the last 5 years has been met or exceeded.