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The part that really called my attention is this one: >>Cells pick up damage all the time, either through environmental exposures or simply as a byproduct of t
by felipemnoa 8y ago
The part that really called my attention is this one:
>>Cells pick up damage all the time, either through environmental exposures or simply as a byproduct of their normal metabolism. If the damage is sufficiently critical, the cell will respond by committing an orderly sort of suicide called apoptosis, which keeps it from causing any further problems. For lesser damage, there's a less drastic alternative called senescence, in which the cell remains active and contributes its normal functions to the organism's health, but it commits to no longer dividing.<<
Old people, lots of senescence cells no longer dividing, young people, lots of young cells still dividing. Aging kind of makes sense when looked at it this way. As long as cells are able to keep dividing you may be able to stay relatively young.
Knowing nothing else it seems that you must keep the number of senescence cells low to keep the effects of aging at bay. Of course, it is probably much more complicated than this. At a minimum this may be a piece of the puzzle to figure out long life.
- toomuchtodo 8y agoCan you imagine if one of the cures to aging is safely removing senescent cells from the body? I'm not going to say its easy by any means, but it does seem straightforward in an unexpected way ("right under our noses"). Very exciting times in biomedical research. My hope is that anti-aging quickly accelerates into an industry instead of basic research (requiring checks, balances, all that jazz to keep the snake oil salesman and quacks at bay), which should allow for orders of magnitude of funding to flow into finding protocols for treatment (from an aging populace). Eagerly awaiting reasonattlm's take on this.
- felipemnoa 8y ago>>Can you imagine if one of the cures to aging is safely removing senescent cells from the body? At a minimum it seems that we are on the right track. Pretty exciting times.
- ars 8y agoYou have to be careful not to cause cancer in the process. From what I read, a lot of the things the body does, which have aging as a side effect, are intended to block cells from becoming cancerous. For example a senescent cell - it might be damaged, and if it dived it might become a cancer, so better stop it from dividing. But we still need it, so don't kill it off. Now you might think - actually, let's kill it and let some other cell divide and replace it. But that creates more cell division, which are more opportunities for cancer. Basically, it's a delicate balance. I suspect a different balance is also possible (there are animals without cancer for example), but the hard part is you must change all the parts at once (into the new balance), and simply stopping one part of the process will cause cancer. This is going to make the research very hand without truly understanding all the moving parts, and joining all the different treatments into a single working whole. What's needed is a fast-living animal, that ages, and gets cancer, in the same way humans do. Then you can just experiment without understanding.
- bachmeier 8y ago> What's needed is a fast-living animal, that ages, and gets cancer, in the same way humans do. Then you can just experiment without understanding. A simulated human?
- philipkglass 8y agoSadly, no. Cells are very complex. Whole multicellular organisms are even more complex. We don't have models nearly good enough to replace laboratory experiments with E. coli, much less good enough to replace medical trials with humans.
- derefr 8y agoDo we need to understand anything about how a multicellular organism works, if we have 1. a working model of biology on the intracellular level, and 2. a working model of stereochemistry outside the cell, and use these to just "play out" cell division from an initial gamete within a simulated womb? (I know that's A Lot of computing power, but maybe an algorithm like HashLife could make this possible by, say, 2100?)
- philipkglass 8y agoIf it's possible to do something like this at all, I think it must be based on techniques largely yet-to-be-discovered. To accurately model biology on the intracellular level, you need a "map" of the cell down to the molecular level, plus fast, general, highly accurate methods for simulating molecular-level chemistry. For the chemical simulation side of things, it would take many centuries of continued Moore's Law progress to make today's most accurate algorithms for fully quantum chemistry run fast enough. And the wild ride of Moore's Law already appears to be closer to its end than its beginning. We'd need fundamental algorithmic breakthroughs to make it feasible without relying on better simulation hardware solving the problem. That might be possible, but I don't when/how/if such algorithms may appear. On the problem of getting a ground-truth molecular map of a cell in the first place, we know that there are many gaps in current models. We're not sure where all of them are. Even if you had the fast, efficient, vast molecular simulation capacity I sketched above, it would still take a lot of experiment/simulation comparisons to be sure that all the biologically relevant features had been captured in the original model. Even now I'm probably badly understating all the problems on the biology side. I worked at the interface of chemistry, biology, and chemical physics, but I was more familiar with the software/physics side of things. I learned just about enough biology to be useful in my role and to be grateful that even my most complicated debugging sessions didn't involve 3 billion years' worth of undocumented legacy code running on wet nanotechnology.
- 21 8y ago> Can you imagine if one of the cures to aging is safely removing senescent cells from the body? Very rarely are things in biology so simple. Everytime we thought something was useless in the past (junk DNA, appendix, tonsils, ...) it turned out that removing it causes damage somewhere else.
- DenisM 8y agoThe key aging problem is that DNA damage is accumulating over the lifetime. Some cells reach apoptosis, some reach senescence, some reach cancer, some keep on being normal for a while. Culling senescent cells does not undo the accumulated damage. You are making room both for cancerous and normal cells. Normal cells are still damaged though. I'm guessing the net contribution is still positive, but the specter of cancer is still looming. On the bright side, I hope that cancer can be managed purely mechanically. Imagine dropping by for your weekly ultra-targeted radiation therapy to kill this week's tumors before going for lunch.
- mettamage 8y agoSilly question: how difficult would it be to extract your DNA code into digital format and then create cells based on that digital formatted DNA and put them into your body? Note: not at all a biologist as you can probably see from the way I phrase things :)
- Koshkin 8y agoI'd rather have my cells replaced with transistors - one by one. That way I might have a chance to outlive that radio made in 1960...
- derefr 8y agoI imagine it'd be far easier to just extract existing stem cells from the body, freeze them, and then every once in a while wake them up, culture some, and re-seed the body with them.
- meowface 8y ago> Imagine dropping by for your weekly ultra-targeted radiation therapy to kill this week's tumors before going for lunch. I suspect if we ever reach such a distant future, we'll consider most radiation therapy to be a very blunt and barbaric instrument (even if ultra-targeted) and use some kind of nanotechnology instead. Some engineered virus or bacterium or nanomachine that hunts down the carcinogenic cells.
- 738472527784 8y ago