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"Jeff Findley" wrote in message
... Keep fighting the good fight OM. You ought to know your body better than anyone else, right? Oh no, I think there's that one lady at the "Pancho's Bar and Grill and Dancehouse" that knows his body pretty well. :-) -- Greg Moore SQL Server DBA Consulting Remote and Onsite available! Email: sql (at) greenms.com http://www.greenms.com/sqlserver.html |
#22
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On Fri, 18 Apr 2008 20:42:57 -0400, in a place far, far away, "Rhonda
Lea Kirk" made the phosphor on my monitor glow in such a way as to indicate that: Rand Simberg wrote: On Fri, 18 Apr 2008 09:55:42 -0500, in a place far, far away, Pat Flannery made the phosphor on my monitor glow in such a way as to indicate that: Non-existence versus existence in this world is a lot like considering the lesser of two evils, and frankly at times the non-existence alternative looks a lot less intrusive on Earth's ecology and more theologically sound overall. ;-) By what theology? And when did "earth's ecology" (whatever that means...) become the highest value? http://www.vhemt.org/ Exactly. And I'm not shocked at all to find Pat sympathetic. But then, we've always suspected that he's not really human... |
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"Pat Flannery" wrote in message news:VN6dnchVaMa3cprVnZ2dnUVZ_t2inZ2d@northdakotat elephone... Latest from OM, who apparently has become a television-watching dope fiend, with a morphine monkey on his back. glad to see Stumpy's back to normal so soon g -- Terrell Miller "If computers get too powerful, we can organize them into a committee - that will do them in." - Bradley's Bromide |
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On Apr 18, 12:50*am, Pat Flannery wrote:
wrote: I got my new Scientific American this evening and looked through it. They had an article about limb regeneration in mammals. * I saw something about OM here in these newsgroups, and for some reason thought I should post that fact here. http://www.sciam.com/article.cfm?id=...ng-human-limbs Good luck. I'll forward this to him; I still think that amphibian DNA is the key. :-) Pat Yes it would be awesome wouldn't it? I'm thinking about all those kids who were dismembered by mines throughout the world. Princess Diana supported that cause when she was alive. |
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In article , Rand Simberg
wrote: On Fri, 18 Apr 2008 09:55:42 -0500, in a place far, far away, Pat Flannery made the phosphor on my monitor glow in such a way as to indicate that: Non-existence versus existence in this world is a lot like considering the lesser of two evils, and frankly at times the non-existence alternative looks a lot less intrusive on Earth's ecology and more theologically sound overall. ;-) By what theology? Pat was just pointing out that his existence is proof that there is no God. But we already knew that. -- David M. Palmer (formerly @clark.net, @ematic.com) |
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I think it has to do with the telomeres at the end of the DNA not the
DNA proper. Basically, when you cut of a salamandar's limb, instead of scarring over, it triggers the same mechanism that occured in the embryo in the first place. The same mechanism starts in humans, but then is interrupted. The trick is to fool the growing scar, into thinking its back in the embryo, and get the stump to grow a complete limb - THEN STOP - telomerase - which is present in small quantities in the embryo, but not in adult animals - is a powerful mutagen and carcinogen. So, that's why I think telomeres are involved. Also, shortening of the telomeres is associated with aging. Telomerase has been known to lengthen telomeres. Alright a little recap of biochem 101 - for those who are lost at this poin. All animals are made of cells. All animal cells can be thought of as tiny water balloons - the balloon itself is the cell membrane, the water is called cytoplasm - think of a water balloon filled with broth. Inside each cell is a tiny center - think of a tiny whiffle golf ball inside the broth filled water balloon. Inside the whiffle ball is a set of zippers - zipped together. The zippers have a lot of little hooks that fit together. There are four kinds of hooks that operate in two pairs. A C G and T they're called. A sticks with C and G with T - each pair is like a logical zero and one - the zippers in thisway store information. Now the zipper have two tricks - expression and replication. Expression A 'fly' can cruise along and unzip the two lines of hooks - and expose the 'naked' hooks to the broth. In the broth are floating around free floating hooks, of more types than just these four. They're unzipped 3 at a time, and based on the six hook ends that present themselve through the 'fly' to the solution, a particular hook from solution is drawn in, and an complementary chain of hooks is formed. This string floats off and bumps into other structures, and folds up into a useful cellular machine. In fact all parts of the cell ismade of stuff fromthe broth in this way. so, this is howinformation gets expressed as operating machinery within the cell. Replication the other trick is that the two sides of the zipper can be undone, leaving two entirely naked lines, and a complementary line is drawn out of solution - now you have TWO complete zipper pairs where you had one before. These two get expressed at the same time, and they sort of fight with each other, forming a wall between them, and where you had one cell before, now you have TWO. Now the machinery that gets made and is operating in the cell is incompletely understood. One interesting thing to think about - when thinking about regeneration - is how the heck to groups of cells create structures like bones nerves veins arteries skin, hair you name it... well, here's the best idea... the cell membranes have sticky spots on them, just like a black and white dog has spots on him. these sticky spots are ony sticky to other particular sticky spots. Sort of like a molecular lock and key. In fact this lock and key idea, ishow information gets transmitted between cells - and that's incompletely understood as well. but back to how this system creates structures... Imagine the cells are a bunch of ping pong balls in a shoe box. If they don't stick to one another - you put the balls in and shake them - the equivalent of heat action - you don't get any structure. You cover them with contact adhesive, and you put them in and shake the box, and you get an undifferentiated blob!! more interesting than before, but not by much. Now, you put two spots on each ball - one at the north pole, one at the south pole, and this glue is special it only sticks to another spot, not the box or parts of the ball that don't have glue on it. call it grue. so you put these grue covere balls in a shoe box, shake it and voila' - you get a nice single line of ping pongballs. Change the position of one of the spots - moving it 5 degrees off the pole toward the equator - and you get circle!!! Now imagine you have different colors of grue that only stick to the same colored grue - and you can see that by creating different breeds of cells that change their spots as they divide, you can create very sophisticated structures!!! What are telomeres again? haha.. they're the heavy molecules at the end of each of the zippers that hold the two lines of hooks together. In the embryo, they get replicated along with the zippers when the divide. In the adult they get split up and divided like splitting the china in a divorce. After about 50 doublings, there isn't much left, and the cells stop dividing - they become what is known as senescent - senile cells - and that's when you have noticeable aging effects in the organism. Telomerase is a hormone - that tells the zipper to exress telomeres before it replicates. That way when the two zippers are looking around for telomeres, there are plenty to go around. So, it is likely that once we figure all this out - we will not only be able to regrow limbs - but control cancer, and aging effects as well. Which is a sweet deal. How far off is this? Well lets look at the statistics, in 1900 people lived to about 43 and died. Some lived longer some lived shorter lives - but this was the average. In 2000 people lived to about 78 and die. Again, some longer some shorter this is the average. The interesting thing is when you look at the INCREASE in age at death each year year by year. You see that the INCREASE is itself INCREASING every year. And when you plot that rate of increase and project it forward, you can see that there will be a time when the average age will increase by more than one year with each passing year. Do you know when THAT will happens? 2010 - 2012 time frame. Most people alive and well past 2012 - will likely be alive and well - at any time thereafter. Something to think about. What major changes can we expect? Well, what major changes have medical advances wrought in our past? Well, the last time a medical breakthrough had significant social consequences was the invention of anesthetics. Before anesthetics people generally went through life miserable having nothing for the pain. After the first generation of people lived with anesthetics, we had a population with a fundamentally different view toward life. Pain was treatable - not a given. This had a huge effect. This included a great sense of optimism - if science could do this, what else could science do? It was a great boon, and 19th century science optimism was to a large degee due to this great medical success. Another aspect was greater sensitivity to pain. Not just one's own pain, but the pain of others as well. So you see arising up in this pain free generation anti-vivisectionist societies, and anti-slavery movements. This resulted in an end to slavery. At the start of the 19th century, in 1801 - slavery was considered natural and right - a better man benefitted both himself and the lesser man, by taking charge of the lesser man's affairs that the lesser man couldn't manage himself. By 1901 the start of the 20th century, no civilized human being defended slavery due to understanding the great emotional hardship is created - regardless of the economic cost to both slave and slave owner. This was all brought about by anesthetics. It seems reasonable that if people live forever due to advances in science - we will have a similar sensitivity toward killing for any reason. The same attitude most people have toward harming infants or children, will be transferred to everyone, since in effect medical science will make of us children with very long lives. Furthermore, unlimited aging in vital vibrant bodies - will create a sense of optimism and open ended possibility that will restore much of the optimism of 19th century science. Finally for those who worry about over population, don't! As living standards rise from subsistence level reproductive rates rise as medicine becomes available. But beyond a certain industrial level, reproductive rates fall - below replacement levels at current longevity. As humanity becomes space faring, the density of humans will drop far from Earth - as we spread across the galaxy. This will dominate over any longevity increase. |
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David M. Palmer wrote: By what theology? Pat was just pointing out that his existence is proof that there is no God. But we already knew that. Taking that concept seriously though, Hinduism shoots for as many people as possible working up through the ecosystem via reincarnation and eventually leaving Earthly existence altogether. Buddhism considers being born a unlucky bad break, and the rest of their philosophy being a attempt to get through life as damage control. Even Christianity has the concept of Original Sin, so that all children are born tainted to some degree. My concept is closest to Hinduism...we are characters in some sort of computer game played by the gods, and if we are boring enough, they'll delete us from the game; however, if we do wild, violent, and strange things they will keep bringing us back game after game. ;-) Pat |
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http://edtech.clas.pdx.edu/gene_expression_tutorial/
http://en.wikipedia.org/wiki/B-DNA http://en.wikipedia.org/wiki/ImageNA_replication.svg Here is some more detail related to DNA replication and expressoin. * * * * The structure of multi-celled organisms is an interesting subject. The idea of having spots on one cell that only stick to 'locking' spots on another cell is an interesting one. http://en.wikipedia.org/wiki/Recepto...iochemistry%29 Receptor biochemsitry involves protiens that bind only to certain sites. It is but a short step to say that cellular surfaces MECHANICALLY bind to each other in highly specific ways. The evolution of structures in an embryonic organism, or in limb re- growing, I imagine would envolve the EVOLUTION of spot placement as the NUMBER of cells increase. This requires that the EXPRESSION of mechanical bonding spots CHANGE with the number of daughter cells. This requires that the DNA molecule be able to REMEMBER its parent by counting or marking ts replication number - and change the expression of mechanical bonding spots based on which cell it was. Embryos develop structures over time, and there is generally many many more cells produced, and when structures form, there is a cell die- off. These are cells that don't have bonding structures on them, and they are sloughed off - but are important in generating the cells that finally take part in the structure. http://en.wikipedia.org/wiki/Apoptosis I believe it is possible for DNA and DNA polymerase to make temporary notes at the ends of the DNA molecule, using the telomeric chains, and/ or the interface between the telomeric chain and the DNA strand. In this way, the DNA polymerase acts like a TURING MACHINE - reading and writing on a tape to could replications and even uniquely mark cells. http://en.wikipedia.org/wiki/Turing_machine The telomeres likely play an important role in determining precisely WHERE the DNA polymerase 'read/write' head starts when expressing the DNA strand. So, WHAT gets expressed is fixed by the 'count' that is written in the temporary notes - and those expressed items relate to the mechanical spot pattern on the 'skin' of each cell. http://en.wikipedia.org/wiki/Telomere http://en.wikipedia.org/wiki/Telomerase As I mentioned, telomeres occur at the end of a DNA strand, and do not shorten during embryonic development. However, once an organism is born, telomeres are not fully replaced and DO shorten. When they fall below a certain length, after about 50 generatoins, the cells become senescent - and the organism dies shortly thereafter. Telomerase lengthens telomeric chains. It is likely that telomerase operates in a more sophisticated way as a Turing Machine to actually write simple logical marking and counting functions onto the telomeric chain. Resetting the scar tissue to a certain telomeric configuration then, should cause a bud to grow into a limb. Resetting all the cells in the body to an appropriate telomeric configuration should cause the organism's age to be reset. Slowing the shortening of telomeric strands with each cell division should slow the aging process at the cellular level and delay senescence and death due to old age. So, it is expected that we should see the following medical advances occur in the next few years; 1) slow aging process 2) halt cancer process 3) reverse cancer process 4) reset aging process 5) regrow limbs 6) regrow organs |
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Another possibility is the growth of biological systems outside the
body. The creeation of food products for example. A chicken leg, or a side of beef might be grown on demand with far less time, space and materiel than raising a chicken or a cow. Mid-way between a modern farm and a Star Trek style replicator. As I mentioned elsewhere, pressure vessels postulated for free flying space colonies, can be easily adapted to grow crops in greenhouse type environments. Special environments are 10x or more productive than open-air environments. So, creating pressure vessels at very low cost - to produce arable land at less cost than land on Earth, using abundant asteroidal feedstocks and telerobotic labor - is but the first step to lower cost more abundant higher quality food for everyone. Already we have the means to take small fragments of protiens and replicate them in any quantity, using PCR - polymerase chain reaction - technology. http://en.wikipedia.org/wiki/PCR Slight variations in this technique might transform it from a laboratory process to a larger scale production process. One might imagine rather than selling chickens or sides of beef or whole hogs - one could sell a 'seed' for such things that are then grown in a plastic bag over the course of a few days or weeks - providing massive improvements over current or even advanced farming techniques. 1 person per acre - conventional farming 8 persons per acre - green house farming 20 persons per acre - space habitat avanced farming 20,000 persons per acre - 'limb growth' in a test-tube Generally speaking cells are cloned that are similar to a fertilized egg for an organism, but they grow into specific limbs - or organs or parts of animals or plants of interest. Even fast growing plants and animals take longer than 90 days to spawn. Cellular division if promoted and controlled to the degree we're talking about here, has the potential to grow a chicken or a cow limb - in 10 days or so. So, you have a bio-med factory that produces seeds that are stored in a 'development bag' and have a connector to a 'growing machine' similar to the way an inkjet print head is installed in a printer. The 'seed' or 'egg' can be stored in a cool dry place for up to 10 years and still be vital. Two weeks before its needed, its plugged into a growing machine, which reads the ID of the bag, and supplies the appropriate nutrients water and so forth. Specialty chemicals are provided by PCR derived products - feed solutions of appropriate amino acids. Amino acids, carbohydrates, sugars and oils, are supplied by local regeneration plants that take bio-waste and process it back to sterile raw materials through a variety of processes - Generally if a home is supplied water and energy, it has sufficient resources to make whatever sort of food products it has 'eggs' or 'seeds' for. Within two weeks the plant or animal part is fully developed, and ready to be removed from the grower and put into cold storage prior to cooking or processing into the desired meal item. Approximately 200 distint plant and animal products supply every food item, including spices and flavorings, needed to produce any meal possible. A human being eats about 80,000 meals in a lifetime. Each meal requires no more than 10 or 12 plant or animal varieties. So, 1,000,000 'seed' items in cryogenic storage should be able to provide all the meals for a human being over the course of a 72 year span. - this would all fit on the head of pin!!! and take something between the size of a bread box to refrigerator to turn into meals in a week at a rate to provide 21 or more meals per week per person. Again, this is not a replicator in the sense of Star Trek - but it is far more efficient than traditional farming methods. It is something that could fit in an industrial kitchen, and provide meals to hundreds of people nearly automatically. .. |
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