I was taught in high school, and again in university, that cells can only divide 50 times in the human body (whether this istrue for other cases, I’m not sure). The exception to this rule is cancer.
Okay, this is fine, but this has implications! Since the fertilized ovum is a cell (assuming that it’s considered a “new” cell) does that mean that any given human can have a maximum of 2[sup]50[/sup] cells in their entire life?
You are probably thinking of the Hayflick limit. This is roughly the amount of times that a human cell can double cultured in a lab (not in the human body).
well, keep in mind that 2^50 is a truly, colossally, huge number. 1.26x10^15, in fact. 1,260,000,000,000,000, in other words. http://science.howstuffworks.com/cell1.htm suggests that there are in fact 10 trillion cells in a human body, which is 10^12, or one one-thousandth of that number…
Thanks, Epimetheus! However, I notice that that answer still brings up another question which I skirted around in my OP, what counts as the start of the 50? That paragraph says that we are born with a certain number of cells in every organ. Shouldn’t that already have necessitated a number of divisions?
I am not sure what he is getting to tell you the truth. I believe he is saying that past a certain number of divisions, certain cells (some organs, for example) stop dividing expotentially.(sp)
As for the born part. Well, when a person is BORN they are not one cell, so yeah… that does suggest that some division has occured already. The part that counts as the 50 is from the first division on. One cell divides to create two, the one has 49 division left, and the new cell has 50, they both divide, and the first cell has 48, the second cell has 49, and the other two have 50. (as they have not divided yet)
Repeat ad nauseum. Not sure if that repeats your question- not quite sure if that was what you were getting at…
Telomeres exist as “caps” on the end of chromosomes. They get shorter every time a cell divides, and when they get too short the cell generally dies due to chromosomal abnormalities. Hence the estimate that an adult cell can only divide around 50 times.
So, you’re thinking, why haven’t we all died? The answer is that cells in the early embryo have an enzyme called telomerase, which re-lengthens the telomeres to the appropriate length at the begining of gestation - so your parent’s cell divisions are cancelled out. Cancer cells, which are dividing wildly, often re-activate this enzyme, and some other cell types may do so under normal conditions.
While telomerase is obviously necessary in the long run, shortening telomeres don’t seem to play a role in any one lifespan. Researchers have mutated the telomerase gene in mice, thereby stopping ANY cells (including embryonic) from re-lengthening their telomeres. These mice were perfectly happy and fertile through the fifth generation, when their telomeres finally ran out. So, in mice at least, there is more than enough room in the telomeres for all the cell divisions in the adult animal.
The mouse (not rat) mutation was published in Cell, 1997, volume 91, pp25-34. I think that the site won’t let you get more than the abstract without a subscription.
Of course, later studies did show defects in sixth-generation mice, particularly in sperm production and in an inability to form skin cancers, which is consistent with telomerase being required eventually, but not within a single lifespan.
Thanks, so basically that route is not the route towards longer life spans, and telomerase is a dead end? Or is it saying that we have a ways to go before the lifespans reach a point at which telamerase is going to be ncessary to supplant?
Telomerase is not the limiting factor for aging, anyway. I suppose that if we managed to extend our lifespans to 200-300 years, we might need to figure out a way to reactivate telomerase in proliferative tissues (such as blood precursors, gut, skin, and hair). Right now it’s not an issue.