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Monthly Archives: July 2014
Arthritis Alleviated: MetroMD Introduces Latest in Stem Cell Therapy in LA; Promises to be Especially Helpful for …
Posted: July 22, 2014 at 5:41 pm
Los Angeles, CA (PRWEB) July 22, 2014
MetroMD, one of the leading names in regenerative medicines in all of California and one of the greatest proponents of holistic health services, now brings a reason to rejoice for individuals long suffering from debilitating arthritis. As per a report published on March 6 2013, by The Journal of Bone and Joint Surgery on The US National Library of Medicine National Institutes of Health (Ref: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748969/), on an average, around 500,000 revision of knee replacement surgeries were recorded in the US - with the prime reason being osteoarthritis in majority of these cases. And If Mr. Devin Stone, MetroMDs Operations Director is to be believed, the cumulative cost of the treatment is estimated to be around $50 billion every year.
The cost covers hospitals bills, doctors visits, medicine, etc and makes arthritic treatment, which often requires a repeat procedure, a hugely burdensome endeavor. But the fact is, even after spending so much of money, one is not sure about getting fully relieved from the agony that arthritis brings to ones life. Arthritis appears in many forms and the expresses itself as joint pain, stiffness and limited body movement in a patient, says Dr Alex Martin, MD, MetroMDs Director of Medicines. MetroMD, ensures that patients can put aside all these concerns and enjoy complete healing that only an advanced Stem cell therapy for arthritis can promise, says Dr. Martin highlighting the fact regarding how pocket-friendly the treatment is. One can regain a healthy knee, while retaining the health of his/her money bag now with MetroMDs stem cell therapy.
How does MetroMDs Stem cell therapy Work?
MetroMDs stem cell treatment process includes extraction of healthy bone marrow out of the patients body by experts and placing it in a centrifuge. After segregating various elements of blood, the stem cell is isolated and placed with cellular growth promoters (found in platelets). All of these are then inserted into the part of the body, ensuring a quicker tissue-based healing.
Mr. Devin Stone exuded confidence in mentioning that MetroMDs stem cell therapies come as a great alternative to invasive surgeries - making way for easier and quicker knee replacements and arthritic treatment.
Is the stem cell therapy safe?
Dr. Alex Martin says, If you are suffering from chronic joint paint due to arthritis, surgery is not anymore the only answer. Stem Cell Therapy can provide an amazing alternative, where your own cells are used to promote healing inside your body. Medicine has advanced significantly in the last 15 years and persistence with the techniques that were pioneered over two decades ago is illogical- and newer and less invasive procedures are the future of medicine.
Backed by the fact that stem cell treatment is a minimally invasive procedure requiring little or no hospitalization, Dr Martins and MetroMDs stance towards propagating stem cell therapy looks only logical. The procedure is legal and the therapy rendered by MetroMD is in compliance with CFR 21 part 1271 standards. Being a non surgical process, evidently, its the safest and totally side-effect free process.
Dr. Martin welcomes the residents of LA suffering from debilitating arthritic condition to consult an expert at its branches spread across in several parts of Los Angeles - and enjoy an improved quality of life.
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Trying gene therapy to create biological pacemaker
Posted: July 22, 2014 at 4:43 am
WASHINGTON No batteries required: Scientists are developing a biological pacemaker by injecting a gene into the hearts of sick pigs that changed ordinary cardiac cells into a special kind that induces a steady heartbeat.
The study, published on Wednesday, is one step toward developing an alternative to electronic pacemakers, which are implanted in 300,000 Americans a year.
There are people who desperately need a pacemaker but can't get one safely, said Dr. Eduardo Marban, director of the Cedars-Sinai Heart Institute in Los Angeles, who led the work. This development heralds a new era of gene therapy that one day might offer them an option.
Your heartbeat depends on a natural pacemaker, a small cluster of cells it's about the size of a peppercorn, Marban said that generates electrical activity. Called the sinoatrial node, it acts like a metronome to keep the heart pulsing at 60 to 100 beats a minute or so, more when you're active. If that node quits working correctly, hooking the heart to an electronic pacemaker works very well for most people.
But about 2 percent of recipients develop an infection that requires the pacemaker to be removed for weeks until antibiotics wipe out the germs, Marban said. And some fetuses are at risk of stillbirth when their heartbeat falters, a condition called congenital heart block.
For more than a decade, teams of researchers have worked on a biological alternative that might help those kinds of patients, trying such approaches as using stem cells to spur the growth of a new sinoatrial node.
Marban's attempt uses gene therapy to reprogram a small number of existing heart muscle cells so that they start looking and acting like natural pacemaker cells instead.
Because pigs' hearts are so similar to human hearts, Marban's team studied the approach in 12 laboratory pigs with a defective heart rhythm.
They used a gene called TBX18 that plays a role in the embryonic development of the sinoatrial node. Working through a vein, they injected the gene into some of the pigs' hearts in a spot that doesn't normally initiate heartbeats and tracked them for two weeks.
Two days later, treated pigs had faster heartbeats than control pigs who didn't receive the gene, the researchers reported in the journal Science Translational Medicine. That heart rate automatically fluctuated, faster during the day. The treated animals also became more active, without signs of side effects.
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Stem cells aid muscle repair and strengthening after resistance exercise
Posted: July 21, 2014 at 6:48 pm
PUBLIC RELEASE DATE:
21-Jul-2014
Contact: Diana Yates diya@illinois.edu 217-333-5802 University of Illinois at Urbana-Champaign
CHAMPAIGN, Ill. A new study in mice reveals that mesenchymal (mezz-EN-chem-uhl) stem cells (MSCs) help rejuvenate skeletal muscle after resistance exercise.
By injecting MSCs into mouse leg muscles prior to several bouts of eccentric exercise (similar to the lengthening contractions performed during resistance training in humans that result in mild muscle damage), researchers were able to increase the rate of repair and enhance the growth and strength of those muscles in the exercising mice.
The findings, described in the journal Medicine and Science in Sports and Exercise, may one day lead to new interventions to combat age-related declines in muscle structure and function, said University of Illinois kinesiology and community health professor Marni Boppart, who led the research.
"We have an interest in understanding how muscle responds to exercise, and which cellular components contribute to the increase in repair and growth with exercise," she said. "But the primary goal of our lab really is to have some understanding of how we can rejuvenate the aged muscle to prevent the physical disability that occurs with age, and to increase quality of life in general as well."
MSCs occur naturally in the body and may differentiate into several different cell types. They form part of the stroma, the connective tissue that supports organs and other tissues.
MSCs also excrete growth factors and, according to the new study, stimulate muscle precursor cells, called satellite cells, to expand inside the tissue and contribute to repair following injury. Once present and activated, satellite cells actually fuse to the damaged muscle fibers and form new fibers to reconstruct the muscle and enhance strength.
"Satellite cells are a primary target for the rejuvenation of aged muscle, since activation becomes increasingly impaired and recovery from injury is delayed over the lifespan," Boppart said. "MSC transplantation may provide a viable solution to reawaken the aged satellite cell."
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Stem cells aid muscle repair and strengthening after resistance exercise
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Stem cells aid muscle repair, strengthening after resistance exercise
Posted: July 21, 2014 at 6:48 pm
A new study in mice reveals that mesenchymal (mezz-EN-chem-uhl) stem cells (MSCs) help rejuvenate skeletal muscle after resistance exercise.
By injecting MSCs into mouse leg muscles prior to several bouts of eccentric exercise (similar to the lengthening contractions performed during resistance training in humans that result in mild muscle damage), researchers were able to increase the rate of repair and enhance the growth and strength of those muscles in the exercising mice.
The findings, described in the journal Medicine and Science in Sports and Exercise, may one day lead to new interventions to combat age-related declines in muscle structure and function, said University of Illinois kinesiology and community health professor Marni Boppart, who led the research.
"We have an interest in understanding how muscle responds to exercise, and which cellular components contribute to the increase in repair and growth with exercise," she said. "But the primary goal of our lab really is to have some understanding of how we can rejuvenate the aged muscle to prevent the physical disability that occurs with age, and to increase quality of life in general as well."
MSCs occur naturally in the body and may differentiate into several different cell types. They form part of the stroma, the connective tissue that supports organs and other tissues.
MSCs also excrete growth factors and, according to the new study, stimulate muscle precursor cells, called satellite cells, to expand inside the tissue and contribute to repair following injury. Once present and activated, satellite cells actually fuse to the damaged muscle fibers and form new fibers to reconstruct the muscle and enhance strength.
"Satellite cells are a primary target for the rejuvenation of aged muscle, since activation becomes increasingly impaired and recovery from injury is delayed over the lifespan," Boppart said. "MSC transplantation may provide a viable solution to reawaken the aged satellite cell."
Satellite cells themselves will likely never be used therapeutically to enhance repair or strength in young or aged muscle "because they cause an immune response and rejection within the tissue," Boppart said. But MSCs are "immunoprivileged," meaning that they can be transplanted from one individual to another without sparking an immune response.
"Skeletal muscle is a very complex organ that is highly innervated and vascularized, and unfortunately all of these different tissues become dysfunctional with age," Boppart said. "Therefore, development of an intervention that can heal multiple tissues is ideally required to reverse age-related declines in muscle mass and function. MSCs, because of their ability to repair a variety of different tissue types, are perfectly suited for this task."
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Stem cells aid muscle repair, strengthening after resistance exercise
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Researchers Find Gene That Could Make It Easier To Develop Life-saving Stem Cells
Posted: July 21, 2014 at 6:48 pm
July 21, 2014
Michigan State University
Not unlike looking for the proverbial needle in a haystack, a team of Michigan State University researchers have found a gene that could be key to the development of stem cells cells that can potentially save millions of lives by morphing into practically any cell in the body.
The gene, known as ASF1A, was not discovered by the team. However, it is at least one of the genes responsible for the mechanism of cellular reprogramming, a phenomenon that can turn one cell type into another, which is key to the making of stem cells.
In a paper published in the journal Science, the researchers describe how they analyzed more than 5,000 genes from a human egg, or oocyte, before determining that the ASF1A, along with another gene known as OCT4 and a helper soluble molecule, were the ones responsible for the reprogramming.
This has the potential to be a major breakthrough in the way we look at how stem cells are developed, said Elena Gonzalez-Munoz, a former MSU post-doctoral researcher and first author of the paper. Researchers are just now figuring out how adult somatic cells such as skin cells can be turned into embryonic stem cells. Hopefully this will be the way to understand more about how that mechanism works.
In 2006, an MSU team identified the thousands of genes that reside in the oocyte. It was from those, they concluded, that they could identify the genes responsible for cellular reprogramming.
In 2007, a team of Japanese researchers found that by introducing four other genes into cells, stem cells could be created without the use of a human egg. These cells are called induced pluripotent stem cells, or iPSCs.
This is important because the iPSCs are derived directly from adult tissue and can be a perfect genetic match for a patient, said Jose Cibelli, an MSU professor of animal science and a member of the team.
The researchers say that the genes ASF1A and OCT4 work in tandem with a ligand, a hormone-like substance that also is produced in the oocyte called GDF9, to facilitate the reprogramming process.
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Researchers Find Gene That Could Make It Easier To Develop Life-saving Stem Cells
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Stem cells may offer new course of treatment for ALS
Posted: July 21, 2014 at 6:48 pm
ROCHESTER, MN (KARE/NBC) - Seventy-five years ago, Lou Gehrig was diagnosed with the rare, neurological disease, Amyotrophic Lateral Sclerosis at the Mayo Clinic.
On July 4, 1939, he gave his famous farewell speech to baseball fans.
Doctors now have a better understanding of the fatal disease, but apart from medication that may give someone an extra couple of months, there is still no good way to extend someone's life.
Mayo Clinic researchers are working with stem cells to develop a new treatment. A New Brighton woman hopes to benefit.
Linda Leight spends every minute she can with her eight grandchildren. They visit her often at her home.
Time with grandchildren is always precious, but even more so for her because just like baseball legend Gehrig, Leight has ALS.
The disease has slowed her speech.
She has enrolled in a Mayo Clinic study that is testing the safety of taking stem cells and injecting them into a patient's spinal fluid.
"My hope is that I could gain some time," she said.
Read more: http://kare11.tv/1kWk3as
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Stem cells may offer new course of treatment for ALS
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Motoneuron-like cell transplantation and GDNF delivery for repair of SCI
Posted: July 21, 2014 at 6:43 pm
PUBLIC RELEASE DATE:
18-Jul-2014
Contact: Meng Zhao eic@nrren.org 86-138-049-98773 Neural Regeneration Research
Adipose-derived stem cells-transdifferentiated motoneurons after transplantation can integrate in the host cord. However, cell survival has been restricted by a lack of ideal environment for nerve cell growth. Taki Tiraihi, Shefa Neuroscience Research Center at Khatam Al-Anbia Hospital, Iran developed rat models of spinal cord injury (SCI) and injected adipose-derived stem cells-transdifferentiated motoneurons into the epicenter, rostral and caudal regions of the impact site and simultaneously transplanted glial cell line-derived neurotrophic factor (GDNF)-gelfoam complex into the myelin sheath. Motoneurons-like cell transplantation combined with GDNF delivery reduced cavity formations and increased cell density in the transplantation site. The combined therapy exhibited superior promoting effects on recovery of motor function to transplantation of GDNF, adipose-derived stem cells or motoneurons alone. These findings suggest that motoneuron-like cell transplantation combined with GDNF delivery holds a great promise for repair of spinal cord injury. Related results were published in Neural Regeneration Research (Vol. 9, No. 10, 2014).
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Article: "Intraspinal transplantation of motoneuron-like cell combined with delivery of polymer-based glial cell line-derived neurotrophic factor for repair of spinal cord contusion injury" by Alireza Abdanipour, Taki Tiraihi, Taher Taheri (Shefa Neuroscience Research Center at Khatam Al-Anbia Hospital, Tehran, Iran) Abdanipour A, Tiraihi T, Taheri T. Intraspinal transplantation of motoneuron-like cell combined with delivery of polymer-based glial cell line-derived neurotrophic factor for repair of spinal cord contusion injury. Neural Regen Res. 2014;9(10):1003-1013.
Contact: Meng Zhao eic@nrren.org 86-138-049-98773 Neural Regeneration Research http://www.nrronline.org/
AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.
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Motoneuron-like cell transplantation and GDNF delivery for repair of SCI
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Hello Doctor Nandani Gokulchandran On Stem Cell Therapy Treatment 20th July 2014 – Video
Posted: July 21, 2014 at 6:41 pm
Hello Doctor Nandani Gokulchandran On Stem Cell Therapy Treatment 20th July 2014
By: zee chovis taas
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Hello Doctor Nandani Gokulchandran On Stem Cell Therapy Treatment 20th July 2014 - Video
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ViaCyte asks FDA for go-ahead with human trials of cell replacement therapy for diabetes
Posted: July 21, 2014 at 6:41 pm
ViaCyte, a privately held regenerative medicine company developing a cell replacement therapy for the treatment of diabetes, has filed an Investigational New Drug application with the United States Food and Drug Administration, seeking to start a Phase 1/2 clinical trial in patients with type 1 diabetes, it was reported on Friday.
The trial will assess the safety and efficacy of ViaCyte's VC-01 product candidate, a stem cell-derived, encapsulated cell replacement therapy. The company has also submitted a Medical Device Master File to the United States Food and Drug Administration in support of the Encaptra drug delivery system, the device component of the VC-01 product candidate. The company's VC-01 product candidate includes pancreatic progenitor cells, called PEC-01 cells, which are derived from a proprietary human embryonic stem cell line.
Paul Laikind, Ph.D., president and chief executive officer of ViaCyte, said, 'The filing of this IND represents the culmination of many years of research and development by a dedicated team focused on developing a cell replacement therapy for patients with type 1 diabetes and advancing our VC-01 product candidate to human clinical trials. The ViaCyte team has been assisted and supported by the California Institute for Regenerative Medicine (CIRM) a leading organisation focused on advancing the field of stem cell-based technologies, and JDRF, the leading advocacy organisation for patients with type 1 diabetes.'
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ViaCyte asks FDA for go-ahead with human trials of cell replacement therapy for diabetes
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Stem cells: The major developments in modern medicine — Stem cell bank for all – Video
Posted: July 21, 2014 at 1:40 pm
Stem cells: The major developments in modern medicine -- Stem cell bank for all
Stem cell is a simple cell in the body that is able to develop into any one of various kinds of cells. In 1868, German biologist Ernst Haeckel for the first ...
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Stem cells: The major developments in modern medicine -- Stem cell bank for all - Video
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