Nick, I've copied some information from the Gerontology Research Group
mailing list below, which has had many discussions on Turritopsis.
On Thu, Jan 29, 2009 at 5:52 PM, Kingsley G. Morse Jr. <cha...@nas.com> wrote:
> Induction of reverse development in two marine Hydrozoans
> Int. J. Dev. Biol. 51: 45-56 (2007)
> Schmich et all.
>
> Cnidarians are unique organisms in the animal
> kingdom because of their unequalled potential to
> undergo reverse development (RD). The life cycle
> of some species can temporarily shift ordinary,
> downstream development from zygote to adult into
> the opposite ontogenetic direction by
> back-transformation of some life stages. The
> potential for RD in cnidarians offers the
> possibility to investigate how integrative
> signalling networks operate to control
> directionality of ontogeny (reverse vs. normal
> development). Striking examples are found in some
> hydrozoans, where RD of medusa bud or liberated
> medusa stages leads to rejuvenation of the
> post-larval polyp stage. Artificial stress may
> determine ontogeny reversal. We describe here the
> results of experimental assays on artificial
> induction of RD by different chemical and physical
> inducers on two marine hydrozoans, Turritopsis
> dohrnii and Hydractinia carnea, showing a
> different potential for RD. A cascade of
> morphogenetic events occurs during RD by molecular
> mechanisms and cellular patterns recalling larval
> metamorphosis. For the first time, we show here
> that exposure to cesium chloride (CsCl), an
> inducer of larval metamorphosis, may also induce
> RD, highlighting similarities and differences
> between these two master ontogenetic processes in
> cnidarians
>
> The full text is at http://www.ijdb.ehu.es/web/paper.php?doi=062152js&a=f
>
>
>
>
> Reversing the Life Cycle: Medusae Transforming into Polyps and Cell Transdifferentiation in Turritopsis nutricula (Cnidaria, Hydrozoa)
> The Biological Bulletin, Vol 190, Issue 3 302-312, 1996
> Piraino et all.
>
> Organisms develop through a series of stages
> leading to sexually mature adults. In a few cases
> ontogeny reversal is possible, but it does not
> occur typically after the onset of sexual
> reproduction. All stages of the medusa Turritopsis
> nutricula, from newly liberated to fully mature
> individuals, can transform back into colonial
> hydroids, either directly or through a resting
> period, thus escaping death and achieving
> potential immortality. This is the first metazoan
> known to revert to a colonial, juvenile morph
> after having achieved sexual maturity in a
> solitary stage. Selective excision experiments
> show that the transformation of medusae into
> polyps occurs only if differentiated cells of the
> exumbrellar epidermis and part of the
> gastrovascular system are present, revealing a
> transformation potential unparalleled in the
> animal kingdom.
>
> The full text is at http://www.biolbull.org/cgi/reprint/190/3/302
On Fri, Jan 30, 2009 at 4:44 AM, Robert Bradbury
<robert....@gmail.com> wrote:
> Kingsley, please refer to a property by what it *really* is (and not what
> the press may make it out to be). The ability to dedifferentiate is *not*
> the same as "immortality". Until you have actual statistics with respect to
> what fraction of differentiated organisms are able to dedifferentiate and
> then subsequently redifferentiate you have know idea as to the quality level
> of the genome (and therefore the subsequent potential) for "immortality".
> If only 1% of the differentiated cells of this organism can dedifferentiate
> it is hardly immortal! Do you want to be regenerated using only 1% of the
> cells in your current brain?
>
> The bottom line is that genomes decay over time. If you have enough of them
> one can regenerate a functional organism from those which remain relatively
> undamaged. That does little good for those of us who would prefer the
> contents or information state of those currently existing genomes which in
> our brains may be in a semi-damaged state [1].
>
> Robert
>
> 1. Though it is doubtful whether it is the "information state" of the genome
> which is critical relative to the structural content of the neurons and
> their relationships. Lose the cell (e.g. lose the cell structure and its
> relationships to other cells) and lose the information content it may
> contain. The information state of the genome within each cell may be
> secondary with regard to the physical structure of the cell itself except
> in-so-far as you have to preserve the genome in order to preserve the cell.
On Sat, Dec 27, 2008 at 9:56 AM, Robert Bradbury
<robert....@gmail.com> wrote:
> It largely means that it can control its own dedifferentiation. But without
> knowing what its losses (from the population as a group) are during that
> process (or looking at its radiation resistance or knowing whether it has
> undergone atypical genome duplications and evolution) that doesn't tell you
> whether it has "better" mechanisms to resist aging. You might consider what
> would happen to an adult human if we tried this dedifferentiation strategy.
>
> The only organism that I am aware of that has a significantly unusual DNA
> repair strategy is Deinococcus (radiodurans and related species). I believe
> the DOE only has on its list ~5 bacterial species (out of probably thousands
> they may have tested) which demonstrate some radiation resistance. All are
> less resistant than Deinococcus. Radiation resistance and the preservation
> of DNA is *hard* and many species go for survival and replication rather
> than solving the hard problems.
>
> Robert
>
> On Mon, Dec 22, 2008 at 4:19 PM, Kingsley G. Morse Jr. <cha...@nas.com>
> wrote:
>>
>> FYI:
>>
>> "Turritopsis nutricula is the first case in which
>> a metazoan is capable of reverting completely to a
>> sexually immature, colonial, stage"
>>
>> "Thus, it appears that it has cheated death"
>>
>> http://zygote.swarthmore.edu/intro6.html
>>
>> It seems to me that studying Turritopsis nutricula
>> might show us how to live longer.
>>
>> Happy holidays,
>> Kingsley
On Sat, Jan 31, 2009 at 1:13 PM, Bryan Bishop forwarded:
> This theoretically makes it biologically immortal.
Potentially "genetically" immortal.
> would it be possible to isolate the genes that allow it to do this
These would be "dedifferentiation genes" and yes it would be possible
to isolate them. Whether they would work in all organisms depends
upon how the organisms enforce differentiation upon cell types.
> and splice them into the genes of another organism?
Yes, you can splice them in, whether they would work would depend upon
the organism.
> Would the organism be "immortal"? Could this eventually be applied to humans?
It depends whether what you mean is "able to continue forever" (that
is not too hard -- most bacteria and fungi are able to do that) or
"able to continue with some awareness of what one once was and /or
could be". That is harder. It is highly questionable whether the
"Turritopsis nutricula" remembers anything across its transition
stages. Each development into a mature organismal state is probably
"fresh". So one retains no memories, no learning, etc.
You may be able to be immortal biologically but you are not immortal
from a knowledge base perspective.
Robert
For some people, that effectively means living forever.
His main work is in SENS, or engineered negligible senesence, mostly
the idea that we could be replenishing our stem cells every 10 years
so that we don't lose them to natural causes, and hopefully keeping
that up until you hit "longevity escape velocity" and new technologies
are developed quickly enough that you don't, i.e., die beforehand.
Aubrey has been all over the web-
http://www.ted.com/index.php/speakers/aubrey_de_grey.html
http://slashdot.org/article.pl?sid=08/07/09/1845200
The "Do you want to live forever?" article was where I first learned of Aubrey:
http://www.technologyreview.com/articles/05/02/issue/feature_aging.asp
Here's an archive of his papers (~25 MB):
http://heybryan.org/transhuman/Aubrey.zip
I had the opportunity to discuss with him on the Immortality Institute
Sunday Evening Update stream, so the day before, I did a full running
commentary and annotations and notes on all of his papers-
http://heybryan.org/transhuman/kanzure_questions.html
Hope this helps.
My initial response to this is "The guy is a quack." But I don't know
enough about gerontology (or biology in general) to know for sure.
Can anyone offer an informed opinion?
-Dan
Aubrey's publications (bias much?)-
http://www.mfoundation.org/research/adgpubs
The famous corruption in the Technology Review debates-
http://en.wikipedia.org/wiki/De_Grey_Technology_Review_controversy
"... responding, when de Grey's defenders protested that these
articles contained no detailed, scientific criticism of SENS and
amounted to little more than ad hominem attacks, that he would find "a
working biogerontologist" who would thoroughly criticize de Grey's
ideas."
"Pontin later commented that the de Grey article was one of the most
read and most-discussed articles that appeared in Technology Review in
2005. The April 2005 issue of Technology Review contained a reply by
Aubrey de Grey, [4] and numerous comments from readers. [5]
Pontin acknowledged that neither the article by Nuland nor his own
column attempted to disprove de Grey's ideas. He defended his approach
by noting that he "commissioned what I called a 'profile in the style
of The New Yorker'". He argued that his own column was never intended
to address SENS, but was concerned with the more general subject of
science and religion.
As of January 2009, Pontin had failed to find one "working
biogerontologist" to take the time to publicly debunk SENS."
("Prove Aubrey de Grey is a nut, win $20000")
So there's a few things that need to be separated- what exactly is
quack? Stem cell research? Treating aging as a disease
(biogerontology)? Longevity escape velocity? Anyway, I'll forward your
request to the Gerontology Research Group, where I'm sure you can get
an informed opinion from both his opponents, himself and those who
don't care either way (something hard to find, I might point out).
Btw, some of the research for mprize.org and mfoundation.org is
centered around mice, but also some genetics, so I don't know if
raising mice is in the interest of any of the diybioers here :-). Just
an opportunity.