Body Complete Healing Health Medicine Mind Optimum Soul Soul System Vitality

It is impressive to see how rapidly researchers are moving forward with induced pluripotency. Here's another step forward via EurekAlert!: scientists have "used tiny molecules called microRNAs to help turn adult mouse cells back to their embryonic state. These reprogrammed cells are pluripotent, meaning that, like embryonic stem cells, they have the capacity to become any cell type in the body. The findings suggest that scientists will soon be able to replace retroviruses and even genes currently used in laboratory experiments to induce pluripotency in adult cells. This would make potential stem cell-based therapies safer by eliminating the risks posed to humans by these DNA-based methods, including alteration of the genome and risk of cancer. ... [MicroRNAs] are transient, non-coding molecules that do not incorporate into the genome, but promote self-replication and have the potential to induce pluripotency. They do their thing -- turn a somatic cell into an embryonic stem cell-like one -- and then they're gone ... The goal now is to ensure the safety of induced pluripotent stem cells and to differentiate them into cells that can be used to repair damaged tissue and treat disease."

View the Article Under Discussion: http://www.eurekalert.org/pub_releases/2009-04/uoc--utc040809.php
Read More Longevity Meme Commentary: http://www.longevitymeme.org/news/

From Existence is Wonderful: "If you can manage to scrape away enough of the subcultural detritus and personality artifacts that have glommed onto cryonics over the years, what you're left with is: (a) an experiment in tissue preservation, (b) the idea that future technology may someday be able to repair injury and illness not addressable by today's medicine, and (c) a view of death as a process rather than a discrete event. None of these things seem to me particularly irrational or farfetched in and of themselves. Of course in reality you can't actually ignore the cultural connotations and fringe entanglements of something like cryonics. These things must be acknowledged and addressed if one wants to actually have a clear view of the subject, and that's part of what I am trying to do here. E.g., I think the notion of cryonics has been harmed by assertions that it's a means to (even potentially) 'buy immortality'. Immortality, after all, is incoherent - nobody knows how long they or anyone else is going to live, and it might end up being a pretty long time, but it sure as heck isn't going to be forever, any more than having a job gives you a shot at making Infinity Zillion Dollars."

View the Article Under Discussion: http://www.existenceiswonderful.com/2009/04/cryonics-redux.html
Read More Longevity Meme Commentary: http://www.longevitymeme.org/news/

From In Search of Enlightenment: "In the year 2048 the children from my grade 2 class will be the age of many of those in nursing homes today. Globally there will be 2 billion humans alive over the age of 60. And this will bring unprecedented levels of chronic disease (cancer, heart disease, stroke, [Alzheimer's disease], etc.). If there was something we could do to alter this possible future of unprecedented human suffering and disease from becoming a reality, shouldn't we try to avoid it? ... Instead of feeding the next generation of inquisitive thinkers useless platitudes about the importance of switching off lights to save the world we should encourage them to harness the great potential of [our present knowledge of biology to slow or reverse aging itself] ... Given the certainty and severity of the harm of aging you might expect that vast amounts of public funding are being invested in aging research. You might think that the brightest and most talented scientists who long to make the world a better place are being lured into the field. Unfortunately it is very hard to get people to rally behind aging research. This must change. A deceleration of the aging process might make nursing homes a thing of the past. And that would be an enormous achievement that all future generations of humans could enjoy."

View the Article Under Discussion: http://colinfarrelly.blogspot.com/2009/03/appreciating-impact-natural-selection.html
Read More Longevity Meme Commentary: http://www.longevitymeme.org/news/

This research suggests a way in which calorie restriction (which upregulates sirtuins) might be effective in resisting cancer: "The yeast and nematode equivalents of SIRT1 are fountains of youth that stretch lifespan. Whether SIRT1 slows aging in mammals isn't certain, but it's beneficial in other ways. The protein tunes up metabolism, reducing blood levels of glucose and insulin, and might forestall neurodegenerative illnesses such as Alzheimer's disease and ALS. Given its pro-life credentials, you might expect SIRT1 to inhibit cancer. And several studies suggest that it does. But other work indicates that the protein aids tumors. For example, SIRT1 chops off acetyl groups, which can inactivate the tumor suppressor p53. [Researchers] determined SIRT1's effect on the transcription factor c-Myc, whose expression surges in many breast, colon, and liver cancers. The two proteins are tangled in a regulatory loop, the team found. c-Myc latched onto SIRT1's promoter, spurring cells to manufacture more SIRT1. In turn, SIRT1 detached acetyl groups from c-Myc, hastening its breakdown. To test SIRT1's effects on tumor growth, the researchers implanted cancerous cells expressing c-Myc into nude mice that lack immune defenses. Boosting production of SIRT1 blocked tumor formation."

View the Article Under Discussion: http://www.sciencedaily.com/releases/2009/04/090413083311.htm
Read More Longevity Meme Commentary: http://www.longevitymeme.org/news/

Researchers are working, step by step, towards the knowledge needed to reprogram cells to regenerate damage they presently let stand. Here is one small step forward: "A protein that the heart produces during its early development reactivates the embryonic coronary developmental program and initiates migration of heart cells and blood vessel growth after a heart attack ... The molecule, Thymosin beta-4 (TB4), is expressed by embryos during the heart's development and encourages migration of heart cells. ... Tremendous medical progress has been made to counter the damaging effects of heart attacks, but ordinarily, mammalian hearts are incapable of repairing themselves following damage. They are also limited in their ability to form new blood vessels. ... In this mouse study researchers found that TB4 initiates capillary tube formation of adult coronary endothelial cells in tissue culture. The molecule also encourages cardiac regeneration by inhibiting death in heart cells after an injury such as a heart attack and by stimulating new vessel growth. ... We observed that by injecting this protein systemically, there was increased cardiac function after a heart attack. We hope this protein can inhibit cell death that occurs during a heart attack in the short term, and that it may initiate new growth of coronary vessels by activating progenitor cells in the long term."

View the Article Under Discussion: http://www.eurekalert.org/pub_releases/2009-04/usmc-mpd041009.php
Read More Longevity Meme Commentary: http://www.longevitymeme.org/news/