Page 2,289«..1020..2,2882,2892,2902,291..2,3002,310..»

Stem cells turned into cancer-killing immune cells

Posted: August 13, 2013 at 2:44 pm

T cells, colored blue here, move in to attack.

In addition to fighting off invaders that arrive from outside the body, the immune system is also able to identify cells that have gone bad inside the body. Even though cancer cells look a lot like normal ones, immune cells can often tell the differenceenough that people who receive long-term treatments of immunosuppressive drugs have a higher incidence of cancer.

But the immune system clearly has its limits, or cancer wouldn't be a problem.Cancer cells evolve ways to avoid detection or use the immune system's own signals to tamp down its activity.A number of researchers have been looking for ways to reestablish the immune system's superiority, boosting it in a way that it once again clears out cancer cells. One option for doing so has been to simply boost the cells that already recognize a tumor by isolating them and growing them in large numbers in culture.

This doesn't consistently work, however, as it can be hard to identify and isolate tumor-specific immune cells. A team of researchers has figured out a way of taking stem cells, converting them into immune cells, and directing them to attack one type of cancer.

When most people think of immune function, they tend to think of the cells that make antibodies, called B cells. The antibodies they make stick to invading cells and viruses, keeping the invaders from infecting cells and helping to attract immune cells to destroy them. But there's a second branch of the immune system that targets human cells after they become infected. The T cells recognize strange or unfamiliar proteins on the surface of human cells. When they spot them, the T cells attack and kill the infected cell while boosting the rest of the immune response.

Cancer cells can also have odd-looking proteins on their surface. These proteins can be recognized by T cells, which will then attempt to kill the cancer cell. In many cases, these anti-cancer T cells are present in the bodies of cancer patients; they're just not active in large enough numbers to keep the cancer in check. Some researchers have reasoned that getting more of these cells into the body could give the immune system an edge, so they set about isolating them, growing large numbers outside the body and then putting them back into the bloodstream.

For some cancers, initial trials of this technique suggested it could have promise. But it's not always easy to identify and isolate the immune cells that are targeting a cancer, nor is it necessarily easy to grow large numbers of them in culture.

The alternative is to use stem cells, which do grow extremely well in culture and can be available in large numbers. The problem is that stem cells don't start out recognizing anything in particular. In the body, both T and B cells mature through an elaborate process that gets rid of any cells that recognize normal, healthy human proteins and selects for those that actually have a reasonable chance of recognizing an invader. It's simply not possible to put stem cells through a similar process in a culture dish.

The new paper involves a clever solution to most of these problems. The authors started with existing T cells, which would have alreadygone through the selection process that prevents them from attacking normal cells. They then used the techniques that have been developed to induce them to adopt a stem cell fate to grow them up into large numbers.

Most of the results, however, would recognize something other than the cancer involved. So the authors engineered a hybrid receptor, with one part that recognizes a common leukemia protein and another part that plugs in to the normal T cell receptor system. They inserted these into their stem cells, converting all of them into cells that could recognize leukemia. They then converted the stem cells into T cells.

Read the original here:
Stem cells turned into cancer-killing immune cells

Posted in Stem Cells | Comments Off on Stem cells turned into cancer-killing immune cells

Gene repair technique promises advances in regenerative medicine

Posted: August 13, 2013 at 2:44 pm

Scientists have found new evidence to show how early humans migrated into Europe.

Using human pluripotent stem cells and DNA-cutting protein from meningitis bacteria, researchers from the Morgridge Institute for Research and Northwestern University have created an efficient way to target and repair defective genes.

Writing today in the Proceedings of the National Academy of Sciences, the team reports that the novel technique is much simpler than previous methods and establishes the groundwork for major advances in regenerative medicine, drug screening and biomedical research.

Zhonggang Hou of the Morgridge Institute's regenerative biology team and Yan Zhang of Northwestern University served as first authors on the study; Dr. James Thomson, director of regenerative biology at the Morgridge Institute, and Erik Sontheimer, professor of molecular biosciences at Northwestern University, served as principal investigators.

"With this system, there is the potential to repair any genetic defect, including those responsible for some forms of breast cancer, Parkinson's and other diseases," Hou said. "The fact that it can be applied to human pluripotent stem cells opens the door for meaningful therapeutic applications."

Zhang said the Northwestern University team focused on Neisseria meningitidis bacteria because it is a good source of the Cas9 protein needed for precisely cleaving damaged sections of DNA.

"We are able to guide this protein with different types of small RNA molecules, allowing us to carefully remove, replace or correct problem genes," Zhang said. "This represents a step forward from other recent technologies built upon proteins such as zinc finger nucleases and TALENs."

These previous gene correction methods required engineered proteins to help with the cutting. Hou said scientists can synthesize RNA for the new process in as little as one to three days compared with the weeks or months needed to engineer suitable proteins.

Thomson, who also serves as the James Kress Professor of Embryonic Stem Cell Biology at the University of WisconsinMadison, a John D. MacArthur professor at UWMadison's School of Medicine and Public Health and a professor in the department of molecular, cellular and developmental biology at the University of California, Santa Barbara, says the discovery holds many practical applications.

"Human pluripotent stem cells can proliferate indefinitely and they give rise to virtually all human cell types, making them invaluable for regenerative medicine, drug screening and biomedical research," Thomson says. "Our collaboration with the Northwestern team has taken us further toward realizing the full potential of these cells because we can now manipulate their genomes in a precise, efficient manner."

Go here to read the rest:
Gene repair technique promises advances in regenerative medicine

Posted in Regenerative Medicine | Comments Off on Gene repair technique promises advances in regenerative medicine

New gene repair technique promises advances in regenerative medicine

Posted: August 13, 2013 at 2:44 pm

Aug. 12, 2013 Using human pluripotent stem cells and DNA-cutting protein from meningitis bacteria, researchers from the Morgridge Institute for Research and Northwestern University have created an efficient way to target and repair defective genes.

Writing August 12 in the Proceedings of the National Academy of Sciences, the team reports that the novel technique is much simpler than previous methods and establishes the groundwork for major advances in regenerative medicine, drug screening and biomedical research.

Zhonggang Hou of the Morgridge Institute's regenerative biology team and Yan Zhang of Northwestern University served as first authors on the study; James Thomson, director of regenerative biology at the Morgridge Institute, and Erik Sontheimer, professor of molecular biosciences at Northwestern University, served as principal investigators.

"With this system, there is the potential to repair any genetic defect, including those responsible for some forms of breast cancer, Parkinson's and other diseases," Hou said. "The fact that it can be applied to human pluripotent stem cells opens the door for meaningful therapeutic applications."

Zhang said the Northwestern University team focused on Neisseria meningitidis bacteria because it is a good source of the Cas9 protein needed for precisely cleaving damaged sections of DNA.

"We are able to guide this protein with different types of small RNA molecules, allowing us to carefully remove, replace or correct problem genes," Zhang said. "This represents a step forward from other recent technologies built upon proteins such as zinc finger nucleases and TALENs."

These previous gene correction methods required engineered proteins to help with the cutting. Hou said scientists can synthesize RNA for the new process in as little as one to three days -- compared with the weeks or months needed to engineer suitable proteins.

Thomson, who also serves as the James Kress Professor of Embryonic Stem Cell Biology at the University of Wisconsin-Madison, a John D. MacArthur professor at UW-Madison's School of Medicine and Public Health and a professor in the department of molecular, cellular and developmental biology at the University of California, Santa Barbara, says the discovery holds many practical applications.

"Human pluripotent stem cells can proliferate indefinitely and they give rise to virtually all human cell types, making them invaluable for regenerative medicine, drug screening and biomedical research," Thomson says. "Our collaboration with the Northwestern team has taken us further toward realizing the full potential of these cells because we can now manipulate their genomes in a precise, efficient manner."

Sontheimer, who serves as the Soretta and Henry Shapiro Research Professor of Molecular Biology with Northwestern's department of molecular biosciences, Center for Genetic Medicine and the Robert H. Lurie Comprehensive Cancer Center of Northwestern University, says the team's results also offer hopeful signs about the safety of the technique.

See the original post here:
New gene repair technique promises advances in regenerative medicine

Posted in Regenerative Medicine | Comments Off on New gene repair technique promises advances in regenerative medicine

DOH gives health facilities engaged in stem cell therapy until Aug. 31 to register

Posted: August 13, 2013 at 2:41 pm

By: Jet Villa, InterAksyon.com August 13, 2013 8:42 AM

InterAksyon.com The online news portal of TV5

MANILA, Philippines - The Department of Health (DOH) has given all health facilities practicing stem cell therapy and companies importing and producing stem cell products untilAug. 31to apply for accreditation and product registration, respectively.

Nick Lutero, director of the DOH-Bureau of Health Facilities and Services, said it will be considered illegal for facilities to do stem cell procedures if they fail to comply with the requirement.

Papatigil namin ang pag-conduct ng therapy. For those still continuing to practice, I think we have sufficient laws, particularly on the illegal practice of medicine. They could be criminally liable, he said in a chance interview.

Lutero lamented that only five hospitals have applied for registration although the DOH had issued the guidelines on this since March.

We have done preliminary visits sa mga hospitals na ito at mukang based sa initial inspection, merong sufficient compliance sa mga facilities, he said.

Companies importing and producing stem cell products, on the other hand, should apply for registration with the Food and Drug Administration, an agency attached to the DOH.

Products that will not be applied for registration will also be considered illegal after the deadline.

Experimental treatment not for free

Go here to read the rest:
DOH gives health facilities engaged in stem cell therapy until Aug. 31 to register

Posted in Cell Therapy, Stem Cell Therapy | Comments Off on DOH gives health facilities engaged in stem cell therapy until Aug. 31 to register

DOH sets deadline for stem cell therapy accreditation

Posted: August 13, 2013 at 2:41 pm

Manila, Philippines -- Hospitals and health facilities offering stem cell therapy have until August 31 to apply for accreditation from the Department of Health (DoH).

DoH Secretary Enrique T. Ona said a number of hospitals in Metro Manila have already applied for accreditation to perform this "innovative" treatment that has not yet been accepted as standard mode of care in the country since it needs further tests and several more layers of research.

In the first mid-year convention of the Philippine Society for Stem Cell Medicine at the Manila Hotel yesterday, Ona reiterated that stem cell therapy is "the future of medicine."

"Stem cell therapy is not a cure-all medical treatment. Patients have yet to be presented first with standard of treatment, and in many cases, stem cell treatments have to be done in conjunction with other standard modalities of treatment," he said.

The Bureau of Health Facilities and Services (BHFS) of the DoH is accepting the applications for accreditation while a bio-ethics committee and a hospital-based review board will go over the applications and decide on their approval.

Five big hospitals in Metro Manila have already applied for accreditation, said Nick Lutero, chief of the BHFS.

Lutero said initial checks have revealed that these hospitals possess the required equipment needed for the treatment but they would still have to check on requirements set by the Food and Drug Administration (FDA) in relation to the practice.

Lutero said institutions that are offering stem cell treatments can still perform the procedures pending the approval of applications. However, once formal accreditations are already given, unaccredited institutions should cease offering stem cell therapy.

Excerpt from:
DOH sets deadline for stem cell therapy accreditation

Posted in Cell Therapy | Comments Off on DOH sets deadline for stem cell therapy accreditation

Duane Roth: Ecumenical Innovator for San Diego and Biotech

Posted: August 12, 2013 at 11:03 pm

The Xconomy news service today carried
a sterling look at the contributions that Duane Roth, co-vice
chairman of the California stem cell agency, made before his untimely
death as the result of a bicycle accident.
Reporter Bruce Bigelow pulled together
a host of comments concerning Roth's involvement in the San Diego
community, ranging from biotech to action sports companies. The
headline on the piece read, “The Connector Who Wired up a Regional
Innovation Economy.”
At the time of his death at the age of
63, Roth was CEO of Connect, a nonprofit organization that supported
technology and innovation and one that he was credited with reviving.
Bigelow also wrote,

“Once California voters approved a
2004 ballot proposition that authorized the issuance of $3 billion in
grants for stem cell R&D, (Mary) Walshok (associate vice
chancellor for public programs at UC San Diego) said Roth also played
a key role in bringing together UCSD, Scripps, Salk, and
Sanford-Burnham to create the Sanford Consortium for Regenerative
Medicine
. In fact, Walshok doubts whether anyone but Duane Roth could
have brought the four major research centers together.”

Another speaker at the memorial
services Friday attended by about 1,000 persons was Bill Walton, the
former UCLA and NBA great, who grew up in San Diego.
Bigelow wrote,

“Walton, the NBA Hall of Famer who
has led San Diego Sports Innovators as a division of Connect since
2010, said Roth became a business mentor to him. In his comments
Friday afternoon, Walton said Roth inspired him to be a better
person, and he counted Roth among the people who had the biggest
influence on his life—a list that included his own father, UCLA
coach John Wooden, sportscaster Chick Hearn, author David Halberstam,
and Jerry Garcia of the Grateful Dead.”

Bigelow described Roth as an ecumenical
and pragmatic advocate for innovation who could work with persons who
did not always agree with him on all issues. He was a conservative
and active Republican, but his co-vice chair at at the stem cell
agency, Art Torres, former chairman of the state Democratic Party, on
more than one occasion has lauded Roth's ability to work together.
Bigelow wrote about similar remarks
Friday by Don Rosenberg, an executive vice president and general
counsel at Qualcomm.

“'Duane and I were as different as
two people can be,' Rosenberg said during his eulogy at the Church of
the Immaculata
. 'Duane was born in Iowa, baptized in the Mennonite
church, a Republican. And me, raised in Brooklyn, Jewish, a Democrat.
We quickly learned we had more in common. We were kindred spirits. We
liked the same things: Bikes, biking, cars, and people.'”

Source:
http://feedproxy.google.com/~r/blogspot/uqpFc/~3/g7BsEVSkzS0/duane-roth-ecumenical-innovator-for-san.html

Posted in Stem Cells, Stem Cell Therapy | Comments Off on Duane Roth: Ecumenical Innovator for San Diego and Biotech

ExpertBeacon – Nathan Wei – Mesenchymal stem cells can help you in the treatment of osteoarthritis – Video

Posted: August 12, 2013 at 2:46 pm


ExpertBeacon - Nathan Wei - Mesenchymal stem cells can help you in the treatment of osteoarthritis
Learn more at http://expertbeacon.com/mesenchymal-stem-cells-can-help-you-treatment-osteoarthritis/ In this video, Nathan Wei explains how mesenchymal stem c...

By: ExpertBeacon

Continued here:
ExpertBeacon - Nathan Wei - Mesenchymal stem cells can help you in the treatment of osteoarthritis - Video

Posted in Stem Cell Videos | Comments Off on ExpertBeacon – Nathan Wei – Mesenchymal stem cells can help you in the treatment of osteoarthritis – Video

Scientists manufacture meat: Dutch boffins unveil world’s first laboratory-produced beef burger – Video

Posted: August 12, 2013 at 2:46 pm


Scientists manufacture meat: Dutch boffins unveil world #39;s first laboratory-produced beef burger
Dutch scientists served a hamburger made from cow stem cells at a public tasting in London, making bio-engineering and possibly culinary history.

By: JewishNewsOne

Go here to read the rest:
Scientists manufacture meat: Dutch boffins unveil world's first laboratory-produced beef burger - Video

Posted in Stem Cell Videos | Comments Off on Scientists manufacture meat: Dutch boffins unveil world’s first laboratory-produced beef burger – Video

Stem Cell Research Anomaly Results in Talking Moovie Bumper Stickers – Video

Posted: August 12, 2013 at 2:46 pm


Stem Cell Research Anomaly Results in Talking Moovie Bumper Stickers
http://youtu.be/fgRPi2OejO8 Francois leaves Cary with his bus while working at the Farm on S. Abel Street in Milpitas. Mr. Green and Cary come to terms vis a...

By: Cary Silberman

Read the original post:
Stem Cell Research Anomaly Results in Talking Moovie Bumper Stickers - Video

Posted in Stem Cell Research | Comments Off on Stem Cell Research Anomaly Results in Talking Moovie Bumper Stickers – Video

Rules governing expression of developmental genes in mouse embryonic stem cells are more nuanced than anticipated

Posted: August 12, 2013 at 11:50 am

Javascript is currently disabled in your web browser. For full site functionality, it is necessary to enable Javascript. In order to enable it, please see these instructions. 22 hours ago A detailed analysis of the methylation patterns of histone H3 revealed a nuanced picture of the epigenetic rules governing expression of developmental genes in mouse embryonic stem cells. The image shows a ChIP-seq track file example of H3K4me3 at mouse Homeobox (Hox) gene clusters. Credit: Study's authors and Nature Structure & Molecular Biology.

A decade ago, gene expression seemed so straightforward: genes were either switched on or off. Not both. Then in 2006, a blockbuster finding reported that developmentally regulated genes in mouse embryonic stem cells can have marks associated with both active and repressed genes, and that such genes, which were referred to as "bivalently marked genes", can be committed to one way or another during development and differentiation.

This paradoxical stateakin to figuring out how to navigate a red and green traffic signalhas since undergone scrutiny by labs worldwide. What has been postulated is that the control regions (or promoters) of some genes, particularly those critical for development during the undifferentiated state, stay "poised" for plasticity by communicating with both activating and repressive histones, a state biologists term "bivalency."

A study by researchers at the Stowers Institute for Medical Research now revisits that notion. In this week's advance online edition of the journal Nature Structural and Molecular Biology, a team led by Investigator Ali Shilatifard, Ph.D., identifies the protein complex that implements the activating histone mark specifically at "poised" genes in mouse embryonic stem (ES) cells, but reports that its loss has little effect on developmental gene activation during differentiation. This suggests that there is more to learn about interpreting histone modification patterns in embryonic and even cancer cells.

"There has been a lot of excitement over the idea that promoters of developmentally regulated genes exhibit both the stop and go signals," explains Shilatifard. "That work supports the idea that histone modifications could constitute a code that regulates gene expression. However, we have argued that the code is not absolute and is context dependent."

Shilatifard has a historic interest in gene regulation governing development and cancer. In 2001, his laboratory was the first to characterize a complex of yeast proteins called COMPASS, which enzymatically methylates histones in a way that favors gene expression. Later, he discovered that mammals have six COMPASS look-alikestwo SET proteins (1A and 1B) and four MLL (Mixed-Lineage Leukemia) proteins, the latter so named because they are mutant in some leukemias. The group has since focused on understanding functional differences among the COMPASS methylases. The role of mouse Mll2 in establishing bivalency was the topic of the latest study.

Comprehending the results of the paper requires a brief primer defining three potential methylation states of histone H3. If the 4th amino acid, lysine (K), displays three methyl groups (designated H3K4me3), then this mark is a sign of active transcription from that region of the chromosome. If the 27th residue of histone H3 (also a lysine) is trimethylated (H3K27me3), this mark is associated with the silencing of that region of the chromosome. But if both histone H3 residues are marked by methylation (H3K4me3 and H3K27me3 marks), that gene is deemed poised for activation in the undifferentiated cell state.

The team already knew that an enzyme complex called PRC2 implemented the repressive H3K27me3 mark. To identify which COMPASS family member is involved in this process, the group genetically eliminated all possibilities and came up with Mll2 as the responsible factor. Mll2-deficient cells indeed show H3K4me3 loss, not at all genes, but at the promoters of developmentally regulated genes, such as the Hox genes.

The revelation came when the researchers evaluated behaviors of Mll2-deficient mouse embryonic stem cells. First, the cells continued to display the defining property of a stem cell, the ability to "self-renew," meaning that genes that permit stem cell versatility were undisturbed by Mll2 loss. But remarkably, when cultured with a factor that induces their maturation, Mll2-deficient mouse ES cells showed no apparent abnormalities in gene expression. In fact, expression of the very Hox genes that normally exhibit bivalent histone marks was as timely in Mll2-deficient cells as it was in non-mutant cells.

"This means that Mll2-deficient mouse ES cells that receive a differentiation signal can still activate genes required for maturation, even though they have lost the H3K4me3 mark on bivalent regions" says Deqing Hu, Ph.D., the postdoctoral fellow who led the study. "This work paves the way for understanding what the real function of bivalency is in pluripotent cells and development."

Read the original post:
Rules governing expression of developmental genes in mouse embryonic stem cells are more nuanced than anticipated

Posted in Stem Cells | Comments Off on Rules governing expression of developmental genes in mouse embryonic stem cells are more nuanced than anticipated

Page 2,289«..1020..2,2882,2892,2902,291..2,3002,310..»