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Stem Cell Treatment Center Hawaii – Help – Stem Cell …

Posted: October 21, 2014 at 10:48 pm

The Hawaii Stem Cell Treatment Center is not offering stem cell therapy as a cure for any condition, disease or injury. No statements or treatments on this website have been evaluated or approved by the FDA. This website contains no medical advice. All statements and opinions provided by this website are provided for educational and informational purposes only and we do not diagnose or treat via this website or via telephone. The Hawaii Stem Cell Treatment Center is offering patient funded research to treat individual patients with their own autologous stem cells and is not involved in the use or manufacture of any investigational drugs.

The Hawaii Stem Cell Treatment Center does not claim that any applications or potential applications using these autologous stem cell treatments are approved by the FDA or are even effective. We do not claim that these treatments work for any listed nor unlisted condition, intended or implied. It is important for potential patients to do their own research based on the options that we present so that one can make an informed decision. Ay decision to participate in our patient funded experimental protocols is completely voluntary.

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How stress ups depression risk

Posted: October 21, 2014 at 10:48 pm

New York, Oct 21 (IANS): The immune system is crucial to fend off diseases, but if it is hypersensitive to stress, the risk of depression may go up, says new research.

Pre-existing differences in the sensitivity of a key part of each individual's immune system to stress confers a greater risk of developing stress-related depression or anxiety, the findings showed.

"Our data suggests that pre-existing individual differences in the peripheral immune system predict and promote stress susceptibility," said lead author Georgia Hodes from the Icahn School of Medicine at Mount Sinai in the US.

Under normal conditions when the immune system perceives a threat such as an invading virus, inflammatory proteins called interleukins are released by white blood cells as an adaptive mechanism to limit injury or infection.

But the researchers found that interleukin 6 (IL-6) levels were higher in mice that were more susceptible to stress than in stress-resilient mice.

They also found the levels of leucocytes (white blood cells that release IL-6) were higher in stress susceptible mice before stress exposure.

"Additionally, we found that when mice were given bone marrow transplants of stem cells that produce leucocytes lacking IL-6 or when injected with antibodies that block IL-6 prior to stress exposure, the development of social avoidance was reduced," Hodes added.

The findings demonstrated that the emotional response to stress can be generated or blocked in the periphery.

Evidence in the current study is the first to suggest that interleukin 6 response prior to social stress exposure can predict individual differences in vulnerability to a subsequent social stressor.

The study appeared in the journal Proceedings of the National Academy of Sciences.

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California Stem Cell Report: Growing Stem Cells and …

Posted: October 21, 2014 at 10:47 pm

California's nearly 10-year-old effort to develop therapies from stem cells is riding a technology wave that some folks are saying will pick up considerable momentum this year.

That is good news for the state's $3 billion stem cell agency, the California Institute of Regenerative Medicine, which will run out of cash for new grants in 2017 and which is looking for new sources of revenue from the private sector.

He said five clear themes emerged and one involved regenerative medicine. Temple, a former San Francisco Chronicle columnist, quoted James Canton, CEO of the Institute for Global Futures, as saying major strides are in the offing for 2014. In an email to Temple, Canton said,

Another one of Temple's futurists, David Houle, author of The Shift Age, said that sometime between now and 2020, 'our replacementparts will be superior to the parts we are born with.'

Whether the forecasts are correct or whether the IPO trend will continue is a bit beside the point for the stem cell agency. What they can profit from is the fact that this kind of news generates excitement among investors and among those who might be willing to make a major bet on the Golden State's stem cell agency. Fund-raising becomes easier when the public rhetoric is more than optimistic. The band wagon effect takes hold. The visions of hope that entranced 59 percent of California voters in 2004 when they created the stem cell agency seem much closer to reality.

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With Collaboration, Scientists Test Gene Therapy for 'Bubble Boy Disease'

Posted: October 21, 2014 at 10:41 pm

A new variation of gene therapy raises hopes for a safe and effective long-term treatment for X-linked severe combined immunodeficiency syndrome (SCID-X1), a life-threatening heritable disorder.

The research was produced by a collaborative research team from Dana-Farber/Boston Children's Cancer and Blood Disorders Center, along with other institutions participating in an international clinical trial that involved boys from the United States and France.

SCID-X1, dubbed bubble boy disease after a patient who lived for 12 years in a sterile bubble, is a rare genetic disorder that hinders the ability of individuals to combat infections. Because the disease is carried in an X-chromosome recessive pattern, the disorder occurs almost only in males. The resulting mutations inactivate a gene called IL-2 receptor gamma (IL2RG), severely weakening immune system functions. Left untreated, individuals who inherit the disorder usually die within a year.

Previous gene therapy trials conducted in Europe over a decade ago promised dramatic progress, until a quarter of patients developed leukemia about two to five years following treatment. Scientists found that the previously used vectorthe device for transporting the correct gene in therapyinadvertently activated oncogenes, which can cause cancer.

In this new study, the vector in use is a self-inactivating gammaretrovirus, which has a specific sequence deleted that basic research had implicated in the process of inappropriate activation of oncogenes, David A. Williams, chief of the hematology/oncology department at Boston Children's Hospital, wrote in an email.

Of the nine patients who underwent the treatment, eight had survived between 12 and 38 months after treatment. One boy died from a severe infection he was fighting at the time he enrolled in the study.

A single round of therapy restored normal disease-fighting T cell count300 cells or more per microliter of bloodin six of the eight patients. One patient underwent a second round of treatment and remains healthy despite a low cell count. The eighth patient received a hematopoietic stem cell transplant after the therapy led to less than optimal uptake of the virus and failed to stimulate T-cell production, according to Williams.

We feel the surrogate assays for safety look excellent and are very encouraged, Williams said. However, because leukemia can take years to develop (and although some of our patients are now approaching 4 years of [follow-up]) we must be cautious and continue to follow these children closely.

Williams noted that the research was the result of positive collaboration between institutions.

Work by Sung-Yun Pai and Gigi Notarangelo, funding from [Boston Childrens Hospital] (and other childrens hospitals) and [the National Institute of Health] were essential for success, he said. This is the first international collaborative trial in stem cell gene therapy, which was critical for success due [to the] rarity of [this] disease.

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Promise Put to the Test

Posted: October 21, 2014 at 10:40 pm

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Newswise A 26-year-old woman paralyzed after a motor vehicle accident a year ago has successfully undergone a first-in-human experimental procedure to test whether neural stem cells injected at the site of a spinal cord injury is safe and could be an effective treatment.

The procedure, conducted on Sept. 30 under the auspices of the Sanford Stem Cell Clinical Center at UC San Diego Health System and in collaboration with Neuralstem, Inc., a Maryland-based biotechnology firm, is the first of four in the Phase I clinical trial. Post safety testing, its hoped that the transplanted neural stem cells will develop into new neurons that bridge the gap created by the injury, replace severed or lost nerve connections and restore at least some motor and sensory function.

The patient, whose identity remains confidential for privacy reasons, has been discharged and is recovering without complication or adverse effects at home, said Joseph Ciacci, MD, principal investigator and neurosurgeon at UC San Diego Health System.

The spinal cord injury trial is one of three recent ground-breaking stem cell efforts at UC San Diego, supported by the Sanford Stem Cell Clinical Center, to make the significant leap from laboratory to first-in-human clinical trials.

Last month, researchers at UC San Diego Moores Cancer Center and the Sanford Stem Cell Clinical Center launched a novel Phase I trial to assess the safety of a monoclonal antibody treatment that targets cancer stem cells in patients with chronic lymphocytic leukemia, the most common form of blood cancer.

And later this month, the first patient is scheduled to receive an unprecedented stem cell-based therapy designed to treat type 1diabetes in another Phase I clinical trial at UC San Diego.

What we are seeing after years of work is the rubber hitting the road, said Lawrence Goldstein, PhD, director of the UC San Diego Stem Cell program and Sanford Stem Cell Clinical Center at UC San Diego Health System. These are three very ambitious and innovative trials. Each followed a different development path; each addresses a very different disease or condition. It speaks to the maturation of stem cell science that weve gotten to the point of testing these very real medical applications in people.

To be sure, Goldstein said, the number of patients involved in these first trials is small. The initial focus is upon treatment with low doses to assess safety, but also with hope of patient benefit. As these trials progress and additional trials are launched Goldstein predicts greater numbers of patients will be enrolled at UC San Diego and the Sanford Stem Cell Clinical Center and elsewhere.

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Stem Cell Hair Therapy – Hair Regrowth Treatment using Adult Stem Cell from Luminesce – Video

Posted: October 21, 2014 at 6:49 pm


Stem Cell Hair Therapy - Hair Regrowth Treatment using Adult Stem Cell from Luminesce
Do It Yourself - Stem Cell Hair Therapy : http://placesiana.com/stem-cell-hair-loss-therapy Imagine becoming a healthier, much younger, better looking you? Infused with a potent growth factor...

By: Sam Jeunesse

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Stem Cell Hair Therapy - Hair Regrowth Treatment using Adult Stem Cell from Luminesce - Video

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The Stem Cell's Journey – Video

Posted: October 21, 2014 at 2:49 am


The Stem Cell #39;s Journey
DescriptionStem cells have the ability to transform into many different cell types, but Stemmy the stem cell possesses a unique gift: he can transform cells around him into duplicates of himself....

By: Jeff Alu

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Understanding Niche Cells | Science: Out of the Box – Video

Posted: October 21, 2014 at 2:49 am


Understanding Niche Cells | Science: Out of the Box
Johns Hopkins cell biologist Erika Matunis explains how understanding the cells that take care of stem cells may shed light on cancer. To see more Science: Out of the Box videos, visit http://www...

By: Johns Hopkins Medicine

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Parent stem cells controlled by progeny

Posted: October 21, 2014 at 2:49 am

New York, Oct 20 (IANS): Megakaryocytes or large cells found in bone marrow play a critical role in regulating stem cells, found a study.

In fact, haematopoietic stem cells differentiate to generate megakaryocytes in bone marrow. The study is the first to show that haematopoietic stem cells (the parent cells) can be directly controlled by their own progeny (megakaryocytes).

The results could lead to new treatments for patients recovering from chemotherapy or organ transplantation.

"Our results suggest that megakaryocytes might be used clinically to facilitate adult stem cell regeneration and to expand cultured cells for adult stem cell transplants," said lead author of the study Meng Zhao from the Stowers Institute for Medical Research in Missouri, US.

The researchers found that megakaryocytes directly regulate the function of murine (mice) haematopoietic stem cells - adult stem cells that form blood and immune cells and that constantly renew the body's blood supply.

These cells can also develop into different types of blood cells, including white blood cells, red blood cells and platelets.

The researchers discovered that as a terminally differentiated progeny, megakaryocytes regulate haematopoietic stem cells by performing two previously unknown functions.

"Megakaryocytes can directly regulate the amount of haematopoietic stem cells by telling the cells when they need to keep themselves in the quiescent stage and when they need to start proliferating to meet an increased demand," Zhao concluded.

The study appeared in the journal Nature Medicine.

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'Mega' cells control growth of blood-producing cells

Posted: October 21, 2014 at 2:49 am

While megakaryocytes are best known for producing platelets that heal wounds, these "mega" cells found in bone marrow also play a critical role in regulating stem cells according to new research from the Stowers Institute for Medical Research. In fact, hematopoietic stem cells differentiate to generate megakaryocytes in bone marrow. The Stowers study is the first to show that hematopoietic stem cells (the parent cells) can be directly controlled by their own progeny (megakaryocytes).

The findings from the lab of Stowers Investigator Linheng Li, Ph.D., described in the Oct. 19 issue of the journal Nature Medicine, could cause researchers to rethink what they know about the workings of megakaryocytes and potentially lead to new treatments for patients recovering from chemotherapy or organ transplantation.

"Our results suggest that megakaryocytes might be used clinically to facilitate adult stem cell regeneration and to expand cultured cells for adult stem cell transplants," says Meng Zhao, Ph.D., a postdoctoral fellow at Stowers and lead author on the study. Stowers researchers discovered that megakaryocytes directly regulate the function of murine hematopoietic stem cells -- adult stem cells that form blood and immune cells and that constantly renew the body's blood supply. These cells can also develop into all types of blood cells, including white blood cells, red blood cells, and platelets.

Because of their remarkable ability to renew themselves and differentiate into other cells, hematopoietic stems cells are the focus of intense research and have been used to treat many diseases and conditions. The transplantation of isolated human hematopoietic stem cells is used in the treatment of anemia, immune deficiencies and other diseases, including cancer.

Basic research has centered on identifying and characterizing hematopoietic stem cells, however, it is still not clear how hematopoietic stem cells actually work, and how they are regulated because of the complexity of the bone marrow microenvironment. Zhao and his colleagues discovered that as a terminally differentiated progeny, megakaryocytes regulate hematopoietic stem cells by performing two previously unknown functions.

"Megakaryocytes can directly regulate the amount of hematopoietic stem cells by telling the cells when they need to keep in the quiescent stage, and when they need to start proliferating to meet increased demand." Maintaining that delicate balance is important, he adds. "You don't want to have too many or too few hematopoietic stem cells."

These findings are supported by similar research from the laboratory of Paul S. Frenette, Ph.D., at the Albert Einstein College of Medicine, also reported in the Oct. 19 issue of Nature Medicine.

Employing the advanced technology of the Institute's Cytometry, Imaging and Histology centers, the researchers examined the relationship between megakaryocytes and hematopoietic stem cells in mouse bone marrow. In the course of their research, they found that the protein transforming growth factor B1 (TGF-B1), contained in megakaryocytes, signaled quiescence of hematopoietic stem cells. They also found that when under stress from chemotherapy, megakaryocytes signaled fibroblast growth factor 1 (FGF1), to stimulate the proliferation of hematopoietic stem cells.

"Our findings suggest that megakaryocytes are required for the recovery of hematopoietic stem cells post chemotherapy," explains Li. The discovery could provide insight for using megakaryocyte-derived factors, such as TGF-B1 and FGF1, clinically to facilitate regeneration of hematopoietic stem cells, he adds.

Engineering a megakaryocyte niche (a special environment in which stem cells live and renew) that supports the growth of hematopoietic stem cells in culture, is the next step for the researchers. Zhao and his colleagues are also investigating whether a megakaryocyte niche can be used to help expand human hematopoietic stem cells in vitro and stem cell transplantation for patients.

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