[acb-diabetics] new treatment for type 1
Patricia Wolf
plawolf at earthlink.net
Mon Mar 12 15:42:25 EDT 2012
> New Approach to Treating Type 1 Diabetes? Transforming Gut Cells Into
> Insulin Factories
> ScienceDaily (Mar. 11, 2012) ? A study by Columbia researchers suggests
> that cells in the patient's intestine could be coaxed into making insulin,
> circumventing the need for a stem cell transplant. Until now, stem cell
> transplants have been seen by many researchers as the ideal way to replace
> cells lost in type I diabetes and to free patients from insulin
> injections.
> See Also:
> The research -- conducted in mice -- was published 11 March 2012 in the
> journal Nature Genetics.
> Type I diabetes is an autoimmune disease that destroys insulin-producing
> cells in the pancreas. The pancreas cannot replace these cells, so once
> they are lost, people with type I diabetes must inject themselves with
> insulin to control their blood glucose. Blood glucose that is too high or
> too low can be life threatening, and patients must monitor their glucose
> several times a day.
> A longstanding goal of type I diabetes research is to replace lost cells
> with new cells that release insulin into the bloodstream as needed. Though
> researchers can make insulin-producing cells in the laboratory from
> embryonic stem cells, such cells are not yet appropriate for transplant
> because they do not release insulin appropriately in response to glucose
> levels. If these cells were introduced into a patient, insulin would be
> secreted when not needed, potentially causing fatal hypoglycemia.
> The study, conducted by Chutima Talchai, PhD, and Domenico Accili, MD,
> professor of medicine at Columbia University Medical Center, shows that
> certain progenitor cells in the intestine of mice have the surprising
> ability to make insulin-producing cells. Dr. Talchai is a postdoctoral
> fellow in Dr. Accili's lab.
> The gastrointestinal progenitor cells are normally responsible for
> producing a wide range of cells, including cells that produce serotonin,
> gastric inhibitory peptide, and other hormones secreted into the GI tract
> and bloodstream.
> Drs. Talchai and Accili found that when they turned off a gene known to
> play a role in cell fate decisions -- Foxo1 -- the progenitor cells also
> generated insulin-producing cells. More cells were generated when Foxo1
> was turned off early in development, but insulin-producing cells were also
> generated when the gene was turned off after the mice had reached
> adulthood. "Our results show that it could be possible to regrow
> insulin-producing cells in the GI tracts of our pediatric and adult
> patients," Dr. Accili says.
> "Nobody would have predicted this result," Dr. Accili adds. "Many things
> could have happened after we knocked out Foxo1. In the pancreas, when we
> knock out Foxo1, nothing happens. So why does something happen in the gut?
> Why don't we get a cell that produces some other hormone? We don't yet
> know."
> Insulin-producing cells in the gut would be hazardous if they did not
> release insulin in response to blood glucose levels. But the researchers
> say that the new intestinal cells have glucose-sensing receptors and do
> exactly that.
> The insulin made by the gut cells also was released into the bloodstream,
> worked as well as normal insulin, and was made in sufficient quantity to
> nearly normalize blood glucose levels in otherwise diabetic mice.
> "All these findings make us think that coaxing a patient's gut to make
> insulin-producing cells would be a better way to treat diabetes than
> therapies based on embryonic or iPS stem cells," Dr. Accili says. The
> location of the cells in the gut may also prevent the diabetes from
> destroying the new insulin-producing cells, since the gastrointestinal
> tract is partly protected from attack by the immune system.
> The key to turning the finding into a viable therapy, Dr. Accili says,
> will be to find a drug that has the same effect on the gastrointestinal
> progenitor cells in people as knocking out the Foxo1 gene does in mice.
> That should be possible, he says, since the researchers found that they
> could also create insulin-producing cells from progenitor cells by
> inhibiting Foxo1 with a chemical.
> "It's important to realize that a new treatment for type I diabetes needs
> to be just as safe as, and more effective than, insulin," Dr. Accili says.
> "We can't test treatments that are risky just to remove the burden of
> daily injections. Insulin is not simple or perfect, but it works and it is
> safe."
> The research was supported by the NIH (DK58282, DK64819, DK63608), the New
> York Stem Cell Foundation, and the Russell Berrie Foundation.
>
>
>
> ------------------------------------
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