New Stem Cell Research Moves Towards Creating New Organs From Scratch

The creation of human organs out of thin air like a scene out of a sci-fi movie may not be as far off as we think according to local heart experts who are quick to point out new American research.

Dr. Jason Dyck and Dr. John Mullen of the Mazankowski Heart Institute are calling the research conducted by experts at the University of Minnesota ground breaking. The scientists at Minnesota were able to regrow a rat heart and bring it back to life.

The U.S. researchers first scrubbed out the inside of the heart, leaving just a husk by utilizing a process called de-cellularization.

Within days the new organ was grown from scratch. Stem cells from healthy newborn rats were used to re-cellularize the

Homing Stem Cells Created by Modification

In an advance that may prove useful in many areas of stem cell therapy, U.S. researchers have found a way to modify the surface of stem cells to direct them to where they’re needed.

Human mesenchymal stem cells, a type of adult stem cell that is a precursor of bone-forming osteoblast cells, were taken and the surface was modified by researchers at the Biomedical Research Institute at Brigham and Women’s Hospital in Boston. The stem cells were directed through the bloodstream into the bone due to the modification. The cells matured into new bone cells once they were in the bone.

“Without genetically reprogramming a stem cell, which could cause adverse effects, we were able to navigate the cell to a predetermined location — a necessary first step toward achieving tissue regeneration,” study lead author Dr. Robert Sackstein, a bone marrow transplant physician, said in a prepared statement.

“Stem cells must have a routing cue to traffic to where they’re needed, just like you need a Zip code to deliver mail,” Sackstein added.

Seeking out the adhesion molecule E-selectin found on the lining of bone vessels, including those found in the bone, HCELL is a homing receptor. In this study, Sackstein and his colleagues made the cells express the HCELL molecule by modifying the surface of the stem cells.

The cells migrated to bone and made patches of human bone within mouse bone once the modified cells were injected into mice.

The study is expected to be in the journal Nature Medicine in their February print issue, but the study was already published online on January 13th.

First BioArtificial Heart Created: Major Breakthrough Could End Donor Organ Shortage

An unprecedented feat that could signal the beginning of the end of organ shortages has been achieved by doctors who have stripped down and refurbished a dead heart so that it can beat again.

According to the American team, the shortage of replacement hearts and other organs could be overcome with the new research. The need for anti-rejection drugs could also be completely avoided.

The research, conducted by researchers at the University of Minnesota, could pave the way to a new treatment for the 22 million people worldwide who live with heart failure. The journal Nature Medicine described the the world’s first beating, retooled “bioartificial heart”.

To begin, cells were removed from a whole heart. The blood vessel structure, valves, chambers, and full architecture of the heart were left intact, and repopulated with new cells.

“We just took nature’s own building blocks to build a new organ,” says Dr. Harald Ott, a co-investigator who now works at Massachusetts General Hospital. “When we saw the first contractions we were speechless.”

The work has huge implications: “The idea would be to develop transplantable blood vessels or whole organs that are made from your own cells,” said Professor Doris Taylor, director of the Center for Cardiovascular Repair, Minnesota, principal investigator.

Virtually any organ with a blood supply could be created with the new method. The list includes the pancreas, lungs, kidneys, and liver.

Although costs make it prohibitive at present, Taylor is ready to grow a human heart. But she admits that the method is “years away” from being used in hospitals.

“We could begin with human cells and pig or human scaffold now but creating the larger bioreactors (the vessels in which the organs are grown) and generating the reagents and growing enough cells would cost tens of thousands of dollars for each heart at this point.”

“That is just too expensive to answer basic questions. We of course want to move in that direction, but funding is limited. As we can we will go forward – perhaps one heart at a time.”

Individuals face life long immunosuppression after an organ transplant. And over the long term, kidney failure, diabetes, and high blood pressure are the trade off for heart failure when using drugs to prevent rejection. Even getting to the point of performing the transplantation operation is difficult since donor organs are limited.

Researchers believe a new heart created by decellularization is much less likely to be rejected by the body since the heart is filled with the recipient’s own stem cells.

And once placed in the recipient, in theory the heart would be nourished, regulated, and regenerated similar to the heart that it replaced.

“We used immature heart cells in this version, as a proof of concept. We pretty much figured heart cells in a heart matrix had to work,” Professor Taylor says. “Going forward, our goal is to use a patient’s stem cells to build a new heart.”

As for the source of the cells from a heart patient, she says: “From muscle, bone marrow, or heart; depending on where the science leads us.”

Professor Taylor says that decellularization shows potential to change how scientists think about engineering any organ, even though heart repair was the initial goal.

“It opens a door to this notion that you can make any organ: kidney, liver, lung, pancreas – you name it and we hope we can make it,” she added.

According to UK Transplant, 81 people are waiting for heart transplant. Even though 28 patients died while waiting for a transplant last year, 155 patients had their lives saved or transformed by a heart transplant.

Typically, only 3,000 transplants are performed every year, despite more than 9,000 patients making up the waiting list nationally. While waiting, 1,000 people died last year.

A UK Transplant spokesman says: “These developments offer long term hope and long may they continue but the real problem now is a desperate shortage of donated hearts.”

Dr. Tim Chico, Consultant Cardiologist, University of Sheffield, says: “This is an ingenious step towards solving a massive problem. Heart failure (an inability of the heart to pump sufficient blood, usually after a heart attack) is increasing in the UK.”

“A chronic shortage of donors for heart transplantation makes stem cell therapy appealing. The study is very preliminary, but it does show that stem cells can regrow in the ‘skeleton’ of a donor heart. However, it will take a lot of further work to assess whether this will ever be a viable option for patients.”

Professor Wayne Morrison, Director of the Bernard O’Brien Institute of Microsurgery, Melbourne, comments: “This is the first time a whole organ has been tissue engineered outside the body.”

“They have demonstrated that they can create a heart that looks like a heart and is shaped like a heart and, most excitingly, that they can re-establish the blood vessels that were originally there. It is this ‘regrowth’ of the blood vessel cells that gives the potential in the future to connect this structure to a blood vessel in the body and then get circulation to go through it.”

“This very exciting study,” comments Dr. Jon Frampton, University of Birmingham. “Although this is only a first step requiring considerable follow-up development, the study nevertheless represents an exciting breakthrough that will eventually make the prospect of repairing damaged hearts a reality and will also be an approach that can be extended to other organs.”

Dr. Anita Thomas at the Australian Institute for Bioengineering and Nanotechnology, University of Queensland, adds: “There is one more major step to achieve before we can proceed any further: we need to see what happens when these artificial hearts are placed in a recipient animal for any length of time. The authors of the article have the necessary skills and yet have not reported their results. We wait with anticipation for their next publication.”

There have been advances in growing heart tissue in the laboratory but the complex architecture and intricacies of the body’s primary pump have to be mimicked exactly in order to be fully successful. Until now, the problem has been how to create a 3D scaffold that could do this.

This is why “decellulariazation” became the method of choice for Professor Doris Taylor and her colleagues. The process leaves only the extracellular matrix, the framework between the cells, intact, along with the plumbing and heart valves. This is accomplished by using a detergent to remove all the cells from the organ – in this case, an animal cadaver heart.

Taking immature cells that came from newborn rat hearts, researchers injected rat hearts with this mixture and placed the structure in a sterile chamber in the lab to grow. This was done after first removing the cells from both rat and pig hearts using a detergent.

Professor Taylor said the results were very promising. Contractions were observed in the hearts four days after seeding the decellularized heart scaffolds with cells. Even though it was only at two percent of the efficiency of an adult heart, the hearts were pumping eight days later.

A study at of the hearts at the cellular level revealed that the “cells have many of the markers we associate with the heart and seem to know how to behave like heart tissue.”

Heart Failure Treatment with Adult Stem Cells

For many patients who have run out of options, a new treatment could offer new hope.

The treatment is for patients who have had stents, surgeries, and other treatments without success. These patients suffer from severe coronary artery disease and are at great risk for heart attacks and progressive heart failure.

An injection of stem cells being tested by doctors at Chicago’s Rush University Medical Center with the hope that it will alleviate the problems patients have with their hearts.

Medical history may be made by James Campbell. The sixty-eight year old heart patient has volunteered to have an injection administered directly into his heart. The injection will be blind, meaning that he could possibly be injected with a placebo. But hopefully, the injection will be a special type of stem cell. Campbell is participating in a clinical trial to see if new blood vessels can be grown with stem cells.

“If it works, it’s worth it,” Campbell said.

“The hope is that these endothelial progenitor cells will grow and divide and allow and facilitate new blood vessels to enter that region of the heart muscle that’s not getting enough blood and oxygen,” said Dr. Gary Schaer, director of cardiac catherization at Rush.

Campbell wants to end the debilitating and chronic chest pain he has suffered for three years. He has survived through a heart attack and two heart surgeries already.

“I can walk maybe 60 to 65 feet and I start having chest pains,” Campbell said.

The day before the injection, Campbell donated his own stem cells like every other patient also enrolled in the trial.

“The advantage of the patient’s own stem cells is there’s no chance of rejection,” Schaer said.

Dr. Schaer says the no ethical issues come into play for this treatment. Several dozen patients like Campbell have been injected by Dr. Schaer using 3-D computer mapping and sophisticated catheter technology since the trial started. The results have been incredibly encouraging and there have been no adverse reactions.

“The patients that we’re seeing in follow up, and we’ve seen several that have come back for their one year follow up, we’ve seen marked improvements in their symptoms,” Schaer said.

The current trial is still recruiting patients. But Rush Medical has more trials planned, with different diseases and different kinds of stem cells.

Some of Campbell’s hobbies prior to his heart problems were riding motorcycles and canoing. He is hoping that the injections will alleviate his pain, and allow him to go back to a normal life where he can be active again.

Stem Cells for Spinal Cord Injury

A 38-year old woman has been treated for spinal cord injuries using stem cell therapy. K G Hospital treated and cured a heart patient with stem cell therapy previous to the woman’s treatment as well.

On Friday, Dr. G. Bhaktavasalam, Chairman, K G Hospital, told reporters that after a road accident, the woman suffered paralysis below the neck and lost movement in her limbs due to spinal cord injury.

With a fracture of the neck bone, she was diagnosed with a

Animal Stem Cell Treatment Freedoms May Lead to Benefits for Humans

The controversy over the use of cells from discarded embryos has slowed the research into the medical benefits of stem cells.

But a safer and ethical alternative can be found in adult stem cells. These cells are derived from various sources throughout the human body. These is no chance of immune rejection because a patient can even use his or her own cells.

In animals, where there is less regulation, research using stem cells has progressed far more quickly. The animal version of adult stem cell treatment was documented by ABC’s Nightline.

About 3000 horses have been treated for joint problems said the founder of VetStem in an interview with Nightline. VetStem pioneered the application of this technique. People with house pets, such as cats and dogs, began taking their pets in for the treatment once the news started to spread.

A stem cell infusion was given to a dog with hip dysplasia. A hip replacement would have cost four times the $2500 dollars the stem cell infusion cost. Much greater freedom of movement and a happier more active personality was observed in the dog within two weeks.

Since the firm has refused to release what it says is proprietary information about its methods, researchers have expressed caution about VetStem’s claims for its technique. However, despite the the lack of outside evaluation, pet owners have no doubt about the effectiveness of the stem cell treatments.

The promise of finding treatments to heal not only the joints, but also the kidneys, livers, hearts, and spinal cords injuries of humans could be accelerated if a similar technique can pass the regulatory hurdles for humans.

Stem Cell Bank Proposed by Japanese Researcher

On Wednesday, a Japanese researcher proposed a system that could help reduce the time and money needed for treating patients with regenerative medicine in the future. A new type of stem cell, which is produced from a donor’s ordinary skin cells, would be banked much like umbilical cord blood is today.

Shinya Yamanaka of Kyoto University said that instead of tailor-made treatments for individual patients, the proposed system would be more practical.

In November of 2007, without using human embryos or cloning technology, Yamanaka led one of two teams which were able to transform ordinary human skin cells into cells that look and act like embryonic stem cells.

Ethical debates have swarmed stem cell research for years, but Yamanaka’s Japanese based team, along with another team from the United States quited many by reporting their research last year.

Even though researchers say it will take years before such medicine can be used to treat people, new hopes for regenerative medicine have been kindled by the new type of cell called the induced pluripotent stem cell (iPS cell).

“It may be a good idea to make an iPS cell bank,” Yamanaka told a news conference.

“By making such a bank, we can cut down the cost of treatment and also we can shorten the period which is required for the generation of iPS cells,” he said.

“In reality, tailor-made medicine using iPS cells is not so ideal.”

The way to treating people with injuries as well as diseases like diabetes, Alzheimer’s, and heart disease may be paved with iPS cells. Scientists expect them to improve disease research considerably.

However, cells may be needed within 10 days to treat a spinal cord injury and Yamanaka said it takes about three months to transform a patient’s skin cells into iPS cells. The lag in time is the reason for the banking proposal.

Before iPS cells can be used to treat humans, more testing is needed. Although he expects iPS cells to be clinically useful within ten years, it could be longer before iPS cells are used to treat some of the more challenging diseases said Yamanaka.

Mainstream Adult Stem Cell Treatment Access Less than a Decade Away

On Wednesday, a Japanese scientist who recently broke new ground in the field of stem cells said that the technology could be used to cure diseases and heal injuries within 10 years.

Shinya Yamanaka of Kyoto University said the new technology is so simple that many laboratories are competing to make further breakthroughs. In November, Yamanaka’s team reported the creation of cell that were indistinguishable from those taken from human embryos. They accomplished this feat by reprogramming human skin cells.

It is only a matter of time before this technology is used in hospitals said Yamanaka while meeting with reporters in Tokyo.

“I can tell for some patients and for some diseases it may be not, like, 10 years, but for some diseases I can imagine it can take longer than 10 years,” Yamanaka said.

“That depends on diseases and injuries. There’s no single answer,” he said.

There are 220 different types of cells in the human body, and stem cells which are primitive cells, have the potential to differentiate into any of these.

With the hope that stem cells can replace diseased or damaged cells, tissues, and organs, the therapeutic potential of stem cells is enormous.

Since viable embryos had to be destroyed to extract embryonic stem cells (cells which are thought to have the greatest potential among all stem cells), stem cell research was highly controversial: until now.

Critics of embryonic stem cell research, which include the Roman Catholic Church, praised the discovery. A separate team of U.S. researchers at the University of Wisconsin at Madison, led by James Thompson, also reprogrammed skin cells at the same time as the Japanese team.

The research has since upped the pace. Several laboratories in Japan as well as up to five in the United States have also converted human skin cells into pluripotent stem cells, or iPS cells.

“This is because technology is very simple,” he said. “All you need is a basic technology, cell biology” and “you don’t need special technology or equipments.”

Yamanaka admitted that the many rivals in research make things stressful. But he believes “it speeds up everything, the process, because of the competition.”

“So I think it’s very good for patients who are waiting” for treatment, he said.

Umbilical Cord Blood Bill Proposed by MP

In order to get doctors to offer parents the option of storing their baby’s umbilical cord blood, an MP is set to launch a political bid.

A bill regarding the potentially life-saving technique will be presented to Parliament by Tory MP David Burrowes.

Umbilical cord blood is rich in stem cells. Many diseases can currently be treated using these cells, and with technological advances, many more will be treated in the future.

Since NHS provision is limited to only a handful of trusts, a host of private firms have begun offering the service.

Used to treat anyone who needs stem cells for a blood cell disorder, 2000 samples are taken by the NHS each year to supply the NHS Cord Blood Bank.

But matches have been difficult to find at times. Among those cases, patients in ethnic minority groups are most likely to not find a match.

Cord blood storage is often advertised as an insurance policy by private banks since the cells can be used in the future to treat illness. However the prices for private storage are as high as

Success Builds for Adult Stem Cell Treatments

In an attempt to save 2-year-old Caden Ledbetter, who is suffering from a rare cancer called neuroblastoma which attacks the nervous system, doctors at Medical City Dallas Hospital are using stem cells taken from umbilical cord blood for treatment.

The cancer damaged the cells in his bone marrow, bones, and liver. Doctors are hoping that the stem cells extracted from cord blood, which is Camden’s own and was saved and banked upon his birth, will replace the damaged cells.

Transplant doctors are increasingly using umbilical cord blood as a source of stem cells according to research from the American Academy of Pediatrics. The cord blood derived cells , which are a type of adult stem cell, are ethical — unlike embryonic stem cell extraction, where an embryo must be destroyed in the process. Additionally, embryonic stem cells have never successfully treated a human, even in trials.

Caden is one of thousands of patients being treated with adult stem cells. Recent years have seen remarkable advances in adult stem cell treatment and research.