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What Are Stem Cells? – CSA

Posted: November 15, 2014 at 10:58 am

Stem cell research has been hailed for the potential to revolutionize the future of medicine with the ability to regenerate damaged and diseased organs. On the other hand, stem cell research has been highly controversial due to the ethical issues concerned with the culture and use of stem cells derived from human embryos. This article presents an overview of what stem cells are, what roles they play in normal processes such as development and cancer, and how stem cells could have the potential to treat incurable diseases. Ethical issues are not the subject of this review.1

In addition to offering unprecedented hope in treating many debilitating diseases, stem cells have advanced our understanding of basic biological processes. This review looks at two major aspects of stem cells:

What are stem cells?

Stem cells are unspecialized cells that have two defining properties: the ability to differentiate into other cells and the ability to self-regenerate.

The ability to differentiate is the potential to develop into other cell types. A totipotent stem cell (e.g. fertilized egg) can develop into all cell types including the embryonic membranes. A pleuripotent stem cell can develop into cells from all three germinal layers (e.g cells from the inner cell mass). Other cells can be oligopotent, bipotent or unipotent depending on their ability to develop into few, two or one other cell type(s).2

Self-regeneration is the ability of stem cells to divide and produce more stem cells. During early development, the cell division is symmetrical i.e. each cell divides to gives rise to daughter cells each with the same potential. Later in development, the cell divides asymmetrically with one of the daughter cells produced also a stem cell and the other a more differentiated cell.

Differentiation Potential

Number of cell types

Example of stem cell

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What Are Stem Cells? - CSA

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U.S. lets Mexican woman in to help sick sister

Posted: November 15, 2014 at 10:56 am

A woman who needs a bone-marrow transplant says she is finally getting the help she needs after the U.S. government initially denied her the life-saving donor she knew she needed. Alicia Nino DePalma is a legal U.S. resident. She has leukemia and doctors said that a bone marrow transplant is the best way to regain her health quickly. Her best match was her sister, who lives in Mexico, but the family says the sister was denied a visa. However, things have changed. Channel 2s Amy Napier Viteri was at the airport Friday night as DePalmas sister arrived from Mexico. The family says after the visa was denied, they applied for humanitarian parole and got the green light. Viteri was there as twin brothers Gabriel and Ariel DePalma hugged their aunt, Socorro Nio, who made the long trip. I feel like we're good citizens and us not being able to get that, it was really frustrating at first, said Gabriel DePalma. Gabriel says his mother, Alicia, is a legal U.S. resident. He and his siblings are U.S. citizens, including his brother, a police officer in the city of Brookhaven. He says tests showed Alicia's sister was a perfect match for a bone marrow transplant. The problem: The U.S. Embassy in Mexico denied her request for a visa. They were afraid that she was going to come to the U.S. and stay here not return to Mexico, Gabriel said. Not the case, he insists, saying his aunt plans to return to Mexico, where she owns homes and where her family is. The family hired an attorney and applied for humanitarian parole. Nio also had stem cells removed and transported to Atlanta as a backup. But the trip was approved and she boarded a flight Friday to see her sister for the first time in 16 years. One obstacle gone, a new challenge ahead. It's going to be yet another thing we have to get ready for, because it's not going to be easy, Gabriel said. The family says Alicia will now start a more aggressive round of chemotherapy and radiation before they do the transplant. Her sister will be here for six months in case they need to repeat the process.

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Morgridge scientists find way to keep the lights on for cell self-renewal

Posted: November 15, 2014 at 5:46 am

Nov. 13, 2014

One remarkable quality of pluripotent stem cells is they are immortal in the lab, able to divide and grow indefinitely under the right conditions. It turns out this ability also may exist further down the development path, with the workhorse progenitor cells responsible for creating specific tissues.

A team from the Morgridge Institute for Research regenerative biology group, led by University of Wisconsin-Madison professor and stem cell pioneer James Thomson, discovered a way to impose an immortal-like state on mouse progenitor cells responsible for producing blood and vascular tissue. By regulating a small number of genes, the cells became "trapped" in a self-renewing state and capable of producing functional endothelial, blood and smooth muscle cells.

David Vereide

The finding, to be published in the December 9, 2014 issue of Stem Cell Reports, points to a potential new approach to developing cells in the lab environment for use in drug screening, therapies and as a basic research tool.

"The biggest takeaway for me is the ability to arrest development of these cells," says David Vereide, a Morgridge fellow in regenerative biology and lead author on the paper. "Normally, these cells are ephemeral and get used up while differentiating into specific cell types, but we found a way to interrupt that."

During development, blood and vascular cells are thought to originate from a progenitor cell known as a hemangioblast. This research project identified and imposed six transcription factors on the cells that allowed hemangioblasts to keep proliferating over multiple generations. Transcription factors are proteins that regulate which genes get turned on or off in a genome.

In this case, the transcription factors act to "keep the lights on" in these cellular factories that kept them dividing and expanding, he says.

One exciting element of this research, Vereide says, is it could greatly improve the efficiency of creating cell types that have research and therapeutic value. Progenitor cells, the "sons and daughters" of stem cells that give rise to specific tissue, are usually the end steps in producing the key building-block cells for the body brain, vasculature, bone, etc.

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Morgridge scientists find way to keep the lights on for cell self-renewal

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Eli & Edythe Broad Center of Regenerative Medicine and Stem Cell Research at UCLA – Video

Posted: November 15, 2014 at 5:46 am


Eli Edythe Broad Center of Regenerative Medicine and Stem Cell Research at UCLA
In a specially designed facility that is compliant with FDA Good Manufacturing Practices (GMP) requirements, scientists with the Eli and Edythe Center of Reg...

By: UCLA Eli Edythe Broad Center of Regenerative Medicine and Stem Cell Research

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Eli & Edythe Broad Center of Regenerative Medicine and Stem Cell Research at UCLA - Video

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The Company of Biologists Workshops- From Stem Cells to Human Development – Video

Posted: November 14, 2014 at 9:44 pm


The Company of Biologists Workshops- From Stem Cells to Human Development
The Company of Biologists Workshop #39;From Stem Cells to Human Development #39; took place at Wotton House, Surrey (UK) between the 21st and the 24th of September 2014, and was organised by ...

By: The Company of Biologists

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The Company of Biologists Workshops- From Stem Cells to Human Development - Video

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Lung Institute – Using Stem Cell Treatments to Help Patients – Video

Posted: November 14, 2014 at 9:44 pm


Lung Institute - Using Stem Cell Treatments to Help Patients
Lynn Flaherty and Dr. Burton Feinerman of the Lung Institute join us to discuss how their new practice in Nashville is using unique stem cell treatments to h...

By: NewsChannel 5

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Dr. Marissa on Passion, Purpose, Music and Stem Cell Research with Tina Guo and Deven Patel – Video

Posted: November 14, 2014 at 9:44 pm


Dr. Marissa on Passion, Purpose, Music and Stem Cell Research with Tina Guo and Deven Patel
So what does a popular radio talk show host and a stem cell research pioneer and a electric cellist have in common? Two things...first they are all three rec...

By: Marissa Pei

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Dr. Marissa on Passion, Purpose, Music and Stem Cell Research with Tina Guo and Deven Patel - Video

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Key mechanism, potential target to prevent leukemia found

Posted: November 14, 2014 at 3:02 pm

Researchers have identified two proteins that appear crucial to the development -- and patient relapse -- of acute myeloid leukemia. They have also shown they can block the development of leukemia by targeting those proteins.

The studies, in animal models, could lead to new effective treatments for leukemias that are resistant to chemotherapy, said Reuben Kapur, Ph.D., Freida and Albrecht Kipp Professor of Pediatrics at the Indiana University School of Medicine.

The research was reported today in the journal Cell Reports.

"The issue in the field for a long time has been that many patients relapse even though chemotherapy and other currently available drugs get rid of mature blast cells quite readily," Dr. Kapur said, referring to the cancerous cells that overrun the blood system in leukemia.

"The problem is that the majority of patients relapse because they have remaining residual leukemic stem cells in the bone marrow that are resistant to currently available therapies, including chemotherapy," he said.

Mutations in two cellular structures known as receptors have previously been identified as cancer-causing. Patients with those mutations generally have a poor prognosis, but scientists have been uncertain what mechanism led to leukemia in the stem cells with those mutations.

In the Cell Reports paper, Dr. Kapur, first author Anindya Chatterjee, Ph.D., and their colleagues describe the mechanism that leads to the development of acute myeloid leukemia, identifying two proteins known as FAK and PAK1 as key to the process.

In experiments with mice, the researchers showed that eliminating, or "knocking out," the genes that produce FAK and PAK1 prevented the development of leukemia in mice, even though their bone marrow stem cells contained the cancer-causing receptor mutations. Eliminating the FAK and PAK1 proteins did not prevent the mice from otherwise producing and maintaining a normal blood system, the researchers said.

In additional experiments in mice and human cell tissue samples, the researchers identified several drug compounds that target FAK and PAK1 -- now available for experimental use but not approved for use in humans -- that were just as effective in blocking development of leukemia as knocking out the FAK and PAK1 genes.

The next step is to continue testing and refining those experimental drug compounds to verify their effectiveness for potential testing in human trials, Dr. Kapur said.

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Why Stem Cells Aren't Being Tested in the US – Video

Posted: November 14, 2014 at 2:48 pm


Why Stem Cells Aren #39;t Being Tested in the US
Stem cell treatment is restricted in the United States, and we discuss the reasons the FDA has been so restrictive about the game-changing research and thera...

By: TheLipTV

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UW-Madison researchers discover method to encourage self-renewal of stem cells

Posted: November 14, 2014 at 12:45 am

UW-Madison cell and regenerative biology professor James Thomson and his team of scientists recently made new strides in their extensive stem cell research.

Thomson and his team members from the Morgridge Institute for Research conducted tests and experiments on mice to advance their research, according to a UW-Madison news release.

Results from the trials led to a developed method which eternally preserves progenitor cells in their pluripotent stages. In other words, the stem cells, which eventually transform into specific tissues, will forever remain in a phase with the potential to become one of at least 200 different cell types.

Maintaining pluripotent stem cells in a controlled environment enables them to undergo constant reproduction. The cells will cyclically divide and grow to produce working endothelial, blood and smooth muscle cells.

David Vereide, one of Thomsons associates at MIR, said the cells are able to self-renew through the regulation of a small quantity of genes.

"Normally, these cells are ephemeral and get used up while differentiating into specific cell types, but we found a way to interrupt that, Vereide explained in the release.

He also said their findings bring researchers very close to finalizing medical uses for stem cells.

Thomson said in the release he and his team have ambitions to progress from examining mouse cells to working with human cells, and motivate other experts to uncover even more valuable information on the topic.

"I'm hoping that other scientists who see this get inspired," Vereide said in the release. "If you dig into the progenitor state of any tissue, you will probably find core factors that will drive the expansion of those progenitors in a dish.

The new discovery will be recorded in the Dec. 9 publication of Stem Cell Reports.

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