Scientists regenerate heart muscle in primates
Scientists regenerate heart muscle in primates
Findings bring stem cell therapy for damaged hearts closer to clinical trials
In a major advance, researchers at the University of Washington have successfully restored damaged heart muscle of monkeys using heart cells created from human embryonic stem cells.
The Murry Lab in South Lake Union. Dr. Charles (Chuck) Murry is a professor of pathology, bioengineering and medicine/cardiology. He serves as director of the Center for Cardiovascular Biology and co-director of the Institute for Stem Cell and Regenerative Medicine.
The results of the experiment appear in the April 30 advanced online edition of the journal Nature in a paper titled, “Human embryonic-stem cell derived cardiomyocytes regenerate non-human primate hearts.”
The findings suggest that the approach should be feasible in humans, the researchers said.
“Before this study, it was not known if it is possible to produce sufficient numbers of these cells and successfully use them to remuscularize damaged hearts in a large animal whose heart size and physiology is similar to that of the human heart,” said Dr. Charles Murry, UW professor of pathology, bioengineering and medicine, Division of Cardiology, who led the research team that conducted the experiment. A physician/scientist, Murry directs the UW Center for Cardiovascular Biology and is a UW Medicine pathologist. He holds the UW Arra and Eva Woods Endowed Professorship.
Murry said he expected the approach will be ready for clinical trials in humans within four years.
In the study, Murry, along with Dr. Michael Laflamme and other colleagues at the UW Institute for Stem Cell & Regenerative Medicine, experimentally induced controlled myocardial infarctions, a form of heart attack, in anesthetized pigtail macaques.
The infarcts were created by blocking the coronary artery of macaque for 90 minutes, an established model for the study of myocardial infarction in primates.
Implanted graft of cardiac cells derived from human stem cells (green) meshed and beat with primates’ heart cells (red).
In humans, myocardial infarctions are typically caused by coronary artery disease. The resulting lack of adequate blood flow can damage heart muscle and other tissues by depriving them of oxygen. Because the infarcted heart muscle does not grow back, myocardial infarction leaves the heart less able to pump blood and often leads to heart failure, a leading cause of cardiovascular death.
The goal of stem cell therapy is to replace the damaged tissue with new heart cells and restore the failing heart to normal function.
Two weeks after the experimental myocardial infarctions, the Seattle researchers injected 1 billion heart muscle cells derived from human embryonic stem cells, called human embryonic stem cell-derived cardiomyocytes, into the infarcted muscle. This was ten times more of these types of cells than researchers have ever been able to generate before.
All the monkeys had been put on immunosuppressive therapy to prevent rejection of the transplanted human cells.
The researchers found that over subsequent weeks, the stem-cell derived heart muscle cells infiltrated into the damaged heart tissue, then matured, assembled into muscle fibers and began to beat in synchrony with the macaque heart cells. After three months, the cells appear to have fully integrated into the macaque heart muscle.
On average the transplanted stem cells regenerated 40 percent of the damaged heart tissue, said Laflamme, UW assistant professor of pathology, whose team was principally responsible for generating the replacement heart muscle cells.
The results show we can now produce the number of cells needed for human therapy and get formation of new heart muscle on a scale that is relevant to improving the function of the human heart,” Laflamme said.
Dr. Michael Laflamme, MD, PhD, assistant professor of pathology, and Dr. Charles (Chuck) Murry, MD, PhD, professor of pathology, bioengineering and medicine/cardiology, in the Murry lab at South Lake Union. Murry is director of the Center for Cardiovascular Biology and co-director of the Institute for Stem Cell and Regenerative Medicine.
Ultrasound studies of the macaques’ hearts showed that the ejection fraction, an indication of the hearts ability to pump blood, improved in some of the treated animals but not all. The researchers also found that arteries and veins from the macaques’ hearts grew into the new heart tissue, the first time it has been shown that blood vessels from a host animal will grow into and nurture a large stem-cell derived graft of this type.
The most concerning complications were episodes of irregular heartbeats, or arrhythmias, that occurred in the weeks after the macaques received the stem cell injections, Murry said. None of the macaques, however, appeared to have symptoms during these episodes, which disappeared after two to three weeks as the stem cells matured and became more electrically stable.
Going forward the UW researchers will work to reduce the risk of arrhythmias, perhaps by using more electrically mature stem cells. They also will try to demonstrate definitively that the stem cells are actually strengthening the heart’s pumping power.
These cells have improved the mechanical function in every other species in which they have been tested, so we are optimistic they will do so in this model as well,” Murry said.
James J.H. Chong was the paper’s lead author. Murry was the paper’s senior author. Their co-authors were Xiulan Yang, Creighton W. Don, Elina Minami, Yen-Wen Liu, Jill J Weyers,William M. Mahoney Jr., Benjamin Van Biber, Nathan J Palpant,Jay Gantz,James A. Fugate, G. Michael Gough, Keith W. Vogel, Cliff A. Astley, Charlotte E. Hotchkiss, Lil Pabon, Hans Reinecke, Edward A. Gill, Veronica Nelson, Hans-Peter Kiem, and Michael A. Laflamme.
Murry expressed gratitude to philanthropic donors who have supported UW Institute for Stem Cell & Regenerative Medicine and his work, including Jeff and Susan Brotman, Bill and Marilyn Conner, Tom and Sue Ellison, Mike and Lynn Garvey, the Oki Foundation, the Quellos Group, the Orin Smith Family Foundation and the John H. Tietze Foundation Trust.
This work was supported by NIH grants P01HL094374, R01HL084642, U01HL100405, and P01GM08619 and an Institute of Translational Health Sciences/Washington National Primate Research Center Ignition Award. J.C. was supported by National Health and Medical Research Council of Australia Overseas Training and Australian-American Fulbright Commission Fellowships. X.Y. is supported by an American Heart Association post-doctoral scholarship 12POST11940060. J.J.W is supported by an American Heart Association post-doctoral scholarship 12POST9330030. Washington National Primate Research Center is funded by the NIH, Office of Research Infrastructure Programs (ORIP P51 0D010425).
Source: University of Washington / Michael McCarthy / HSNewsBeat
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