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Thursday, October 6, 2011

Researchers Turn Cloned Human Embryo into Working Stem Cell Line



But wait, there's a catch
Human Embryonic Stem Cells Vojtech.dostal via Wikimedia
Potentially big stem cell news out of the New York Stem Cell Foundation Laboratory today in Nature, though in our experience it’s always good to temper one’s expectations when it comes to these sorts of things. After all, we’ve thought we cracked the code on embryonic stem cell cloning technology more than once, only to find this kind of biology is much more difficult and complex than originally thought. Nonetheless, researchers have reprogrammed an adult human egg to an embryonic state and used it to create a self-reproducing embryonic stem cell line. And that’s a big deal.
But it’s not the holy grail of stem cell research. The cell line they created doesn’t produce true clones containing perfect copies of the donor’s DNA, and therefore are more or less clinically ineffective. But the development does represent a step forward for the field, and answers some important questions plaguing stem cell science.

So here’s where we’re at: Scientists are trying to take an unfertilized egg, swap out the single set of chromosomes in the egg for the two sets of chromosomes in a patient’s adult cells, and initiate a process wherein the egg develops per the instructions of the new DNA.
Usually, this process fails. Cultures stop developing after a division or two. So the NY Stem Cell team went looking for the root cause of failure. Through a series of experiments they found that whatever the problem is, it’s introduced during the removal of the egg’s native single chromosome DNA. So they did what most of us do--they skipped a step.
They just left the native DNA in there and inserted the donor DNA alongside it. The reprogramming worked, and they produced an embryo that developed up to what’s known as the blastocyst stage, where the culture contains nearly 100 cells. At this point, stem cells can be extracted from the batch.
Of course, there’s still the problem of the extra set of chromosomes rattling around in there. This makes the stem cells incompatible with the DNA donor’s tissue, so from a clinical standpoint they are roughly worthless. But from a research standpoint, a step forward is a step forward. With the problem isolated, they are now looking at new approaches to remove the native DNA from the egg that won’t cause the hiccup that halts cell division. That could take awhile, but at least now we think we’re moving in the right direction.

Steve Jobs Has Died, Apple Confirms



Apple.com's Tribute to Steve Jobs apple.com
Incredibly sad news from Apple just a matter of minutes ago: Steve Jobs has died today at the age of 56.
Jobs had fought pancreatic cancer publicly and privately since 2004. Just over a month ago, heofficially resigned as CEO, vowing to be a very active chairman of the Apple board, making today's news painfully abrupt.
Chances are, you encounter something on a daily basis that probably would not exist were it not for the mind of Steve Jobs, truly one of history's greatest technical, even cultural innovators. It's a sad day for all of us here at Popular Science, who daily honor the spirit of innovation Jobs embodied more than anyone else on this planet. He will be dearly missed.
A tribute page on Apple.com quotes from Jobs's successor Tim Cook's message to the company: "Apple has lost a visionary and creative genius, and the world has lost an amazing human being. Those of us who have been fortunate enough to know and work with Steve have lost a dear friend and an inspiring mentor. Steve leaves behind a company that only he could have built, and his spirit will forever be the foundation of Apple."
An email address, rememberingsteve@apple.com, has been established for those who wish to share their thoughts, memories and condolences. All of us here at PopSci extend our best wishes to his family, friends and loved ones.

Fat affects how brain cells talk



THE UNIVERSITY OF QUEENSLAND   

Eraxion_-_active_neurone
“Changes in lipid composition have already been shown to be a factor contributing to the development of dementia in Alzheimer's disease."
Image: Eraxion/iStockphoto
Researchers at The University of Queensland's Queensland Brain Institute (QBI) have taken a significant step towards unravelling the mechanism by which communication between brain cells occurs.

Findings from a study just published in Nature Communications reveals that the lipid (fat) from the membranes of brain cells controls the movement of vesicles containing chemical messengers called neurotransmitters.

QBI's Associate Professor Frederic Meunier, who led the study, says these findings were made possible through experimentation with very selective compounds affecting the membrane.

“Our findings explain how minute changes in the lipid composition of our neurons can have a dramatic effect on the way these cells communicate with each other in the brain,” he says.

“We found that the lipid phosphatidylinositol(4,5)bisphosphate orchestrates the mobilization and movement of secretory vesicles towards the plasma membrane of neurosecretory cells.”

According to Associate Professor Meunier, a better understanding of the mechanism underpinning neurotransmitter release will aid scientists' ongoing fight against the plethora of diseases affecting neuronal communication in the brain.

“Changes in lipid composition have already been shown to be a factor contributing to the development of dementia in Alzheimer's disease,” he says.

“We hope that developing novel compounds targetting the fat lipid composition of biological membranes could ultimately help in the treatment of such brain disorders.”
Editor's Note: Original news release can be found here.