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Getting old may not be inevitable — scientists have found a way to turn back the clock on human and animal cells, making them look and behave like younger versions of themselves.

The researchers also used the method to treat mice with a rare disease that causes them to age prematurely and die early, and found that the method increased the animals’ lifespan by 30 percent. And, when normal mice received the treatment, they appeared to be rejuvenated, with some of their cells healing faster than normal in response to injury.

The researchers said that their findings may help scientists better understand the process of aging. One day, it may be possible to use a similar approach to ward off age-related diseases in humans, and thus improve people’s health and increase their lifespan, they said.

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Dr. Matthew O’Connor from the SENS Research Foundation gives a fascinating talk about this years successful results of the mitochondrial repair project (MitoSENS) and the potential for repairing age-related damage to the mitochondria that SENS proposes. 2017 could be an even better year for progress, please consider donating to the SRF Winter Fundraiser and help them make age-related disease a thing of the past.


Please take a few minutes to watch SENS Research Foundation’s Matthew O’Connor give a Google TechTalk during Google’s Giving Week campaign. The topic is his recently published article on our MitoSENS Research. If you enjoy this presentation and support our work please go to our website and donate today. Your support is critical to our success. You can donate at www.sens.org/donate

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The team showed that a new form of gene therapy produced a remarkable rejuvenating effect in mice. After six weeks of treatment, the animals looked younger, had straighter spines and better cardiovascular health, healed quicker when injured, and lived 30% longer.

Juan Carlos Izpisua Belmonte, who led the work at the Salk Institute in La Jolla, California, said: “Our study shows that ageing may not have to proceed in one single direction. With careful modulation, ageing might be reversed.”

The genetic techniques used do not lend themselves to immediate use in humans, and the team predict that clinical applications are a decade away. However, the discovery raises the prospect of a new approach to healthcare in which ageing itself is treated, rather than the various diseases associated with it.

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Excellent article by Nick Gillespie, Editor-in Chief of Reason. Genetic editing is so far the 21st Century’s most important science—and it’s already being challenged by many as too radical: http://reason.com/blog/2016/12/15/will-gene-editing-technologies-spark-the #transhumanism #CRISPR #Future


The folks behind CRISPR gene editing were runners-up for Time’s Person of the Year. Their creation may win the future for secular China.

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It is looking increasingly likely the mysterious Google Calico have very modest ambitions regarding increased lifespans for humans given the comments made by Dr. Aubrey de Grey and others and the direction they are taking with their research. Modest increases of lifespan over the kind of robust therapies of SENS seems pretty dissapointing.


More about Google Calico and their aim to modestly increase lifespan. People like Dr. Aubrey de Grey and Nathaniel David from rising biotech star Unity.

“To some, Calico’s heavy bet on basic biology is a wrong turn. The company is “my biggest disappointment right now,” says Aubrey de Grey, an influential proponent of attempts to intervene in the aging process and chief science officer of the SENS Research Foundation, a charity an hour’s drive from Calico that promotes rejuvenation technology. It is being driven, he complains, “by the assumption that we still do not understand aging well enough to have a chance to develop therapies.” Indeed, some competitors are far more aggressive in pursuing interventions than Calico is.

They are very committed to these fundamental mechanisms, and bless them for doing that. But we are committed to putting drugs into the clinic and we might do it first,” says Nathaniel David, president and cofounder of Unity Biotechnology. This year, investors put $127 million behind Unity, a startup in San Francisco that’s developing drugs to zap older, “senescent” cells that have stopped dividing. These cells are suspected of releasing cocktails of unhelpful old-age signals, and by killing them, Unity’s drugs could act to rejuvenate tissues. The company plans to start with a modestly ambitious test in arthritic knees. De Grey’s SENS Foundation, for its part, has funded Oisin Biotechnologies, a startup aiming to rid bodies of senescent cells using gene therapy.”

Research subjects at the University of Minnesota fitted with a specialized noninvasive EEG brain cap were able to move a robotic arm in three dimensions just by imagining moving their own arms (credit: University of Minnesota College of Science and Engineering)

Researchers at the University of Minnesota have achieved a “major breakthrough” that allows people to control a robotic arm in three dimensions, using only their minds. The research has the potential to help millions of people who are paralyzed or have neurodegenerative diseases.

The open-access study is published online today in Scientific Reports, a Nature research journal.

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IBM Watson is known for its work in identifying cancer treatments and beating contestants on Jeopardy! But now the computing system has expertise in a new area of research: neuroscience.

Watson discovered five genes linked to ALS, sometimes called Lou Gehrig’s disease, IBM announced on Wednesday. The tech company worked with researchers at the Barrow Neurological Institute in Phoenix, Arizona. The discovery is Watson’s first in any type of neuroscience, and suggests that Watson could make discoveries in research of other neurological diseases.

SEE ALSO: This high-tech E.L.F. is guiding confused shoppers with the help of IBM’s Watson.

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Senescent cell removal holds great potential but are all research approaches equal?


Some scientific commentary on senescent cell clearing (Senolytics) and the different approaches the research community is engaged in.

“Researchers are taking two broad approaches to cellular senescence at the present time. The first is to build therapies that can selectively destroy senescent cells, following the SENS rejuvenation model of periodic removal of damage. If the number of senescent cells is managed so as to keep that count low, then they will not cause further harm. This has the advantage of being straightforward and requiring little further research to put into practice. A range of demonstrated treatments and potential treatments already exist — gene therapies, immunotherapies, senolytic drugs, and so forth — and companies such as Oisin Biotechnologies and UNITY Biotechnology are bringing some of these technologies to the clinic.”

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