Induced Pluripotent Stem Cells: 10 Years After the Breakthrough

Despite Major Progress Toward Disease Therapies, Some Technical and Ethical Challenges Still Lie Ahead

microscopic view of induced pluripotent stem cells
Induced pluripotent stem cells that were reprogrammed from normal adult human tissue and have not yet been differentiated. Image courtesy of Gladstone Institutes

Human cortex grown in a petri dish. Eye diseases treated with retinal cells derived from a patient’s own skin cells. New drugs tested on human cells instead of animal models.

Research and emerging treatments with stem cells today can be traced to a startling discovery 10 years ago when Shinya Yamanaka, MD, PhD, and his graduate student Kazutoshi Takahashi, PhD, reported a way to reprogram adult mouse cells and coax them back to their embryonic state – pluripotent stem cells.

A year later, they accomplished the feat with human cells. For this research coup and his leading role pioneering stem cell work, Yamanaka – who holds academic appointments at Kyoto University and UC San Francisco – was the co-recipient of the 2012 Nobel Prize in Medicine or Physiology.

Induced Pluripotent Stem Cells

The National Institutes of Health defines induced pluripotent stem cells as somatic (adult) cells reprogrammed to enter an embryonic stem cell–like state by being forced to express factors important for maintaining the “stemness” of embryonic stem cells.

The breakthrough provides a limitless supply of induced pluripotent stem cells (iPSCs) that can then be directed down any developmental path to generate specific types of adult cells, from skin to heart to neuron, for use in basic research, drug discovery and treating disease.

The achievement opened up a practical way – and in some critical cases, the only way to directly study human “diseases in a dish,” and track the early stages of both healthy and abnormal development. It also allowed researchers to screen new drugs directly in human cells rather than relying on animal models, which more often than not fail to accurately predict a new drug’s effects on people.

The dazzling iPSC breakthrough has spurred rapid progress in some areas and posed major challenges in others. It has already proved a boon to basic research, but applying the new technology to treat diseases remains daunting. Some types of cells have proved difficult to reprogram, and even the protocols for doing so are still in flux as this is still a very young field.

iPSCs in Basic Biomedical Research

For many basic biomedical scientists, the capability offered by iPSCs technology is like a dream come true, says neuroscientist Arnold Kriegstein, MD, PhD, director of UCSF’s Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research.

We’ve never had unrestricted access to living human brain cells. Now we can take skin cells and grow human cortex in a dish. It’s a game-changer for discovery about early human development.

Arnold Kriegstein, MD, PhD

“Induced pluripotent stem cells have given us a window into human development unlike anything we had before,” Kriegstein said. “I’m interested in the early development of the brain’s cortex. Of course, we’ve never had unrestricted access to living human brain cells. Now we can take skin cells and grow human cortex in a dish. It’s a game-changer for discovery about early human development.”

Kriegstein is enthusiastic about what researchers can learn from “organoids” – a pea-sized stage of a developing organ derived from iPSCs. By this stage, cells are already clumping together and starting to signal and differentiate into what will become the adult organ.

“It’s a very close model of the real thing,” Kriegstein says. “We have recently discovered that even in this early stage, the organoids are able to develop intrinsic organization, including a front-and-back orientation, and different parts start to look like they do in the embryonic brain.”

Some scientific papers have suggested that organoids can model diseases found in adulthood – even disorders of late adulthood such as Alzheimer’s disease.

microscopic image of a human cortex organoid
A human cortex organoid that’s grown in a lab dish. Image by Elizabeth DiLullo
portrait of Arnold Kriegstein
Arnold Kriegstein, MD, PhD, is head of UCSF’s Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research

Even though organoids can reveal developmental steps not seen before, Kriegstein worries that some researchers are getting too far ahead of themselves.

“It’s an embryonic brain,” he stresses. “The longest period of growth we can model would be full fetal development. How likely is it that gene expression, cell signaling and a myriad of other interactions at this organoid stage could accurately represent the development of Alzheimer’s disease, a disease that affects people at 60 or 70?

“I think we need to take some of these studies with a grain of salt. Stem cell technology now is so variable that replication is difficult. We need to establish protocols to reliably compare different methods and then use these standardized methodologies to advance research and treatment. But I am 100 percent convinced that we will get there.”

Building on the Original Breakthrough

Yamanaka currently directs the 500-person Center for iPS Cell Research and Application at Kyoto University, runs a research lab at the Gladstone Institute for Cardiovascular Disease in San Francisco, and serves as a professor of anatomy at UCSF, and Takahashi is a visiting scientist at the Gladstone Institutes and runs Yamanaka’s lab there. Both have continued to build on their iPSC work, as have other researchers.

Shinya Yamanaka working in his Gladstone lab
Shinya Yamanaka, MD, PhD, in his lab at the Gladstone Institutes. Photo by Chris Goodfellow/Gladstone Institutes

In their seminal work, Yamanaka and Takahashi had introduced four genetic factors to prompt adult cells back to the pluripotent state. Soon after their iPSC breakthrough, Sheng Ding, PhD, who has a lab at the Gladstone Institutes and is a professor in UCSF's Department of Pharmaceutical Chemistry, began refining the reprogramming cocktail.

Eventually, Ding was able to substitute drug-like molecules for these gene transcription factors, eliminating the risk of new genetic material altering the cells. Today, labs around the world pursue and tout different chemical recipes, often depending on the type of cell they are trying to reprogram.

Other recent advances to induce pluripotency harness different kinds of proteins that influence gene activity in the cell nucleus. Robert Blelloch, MD, PhD, a stem cell scientist at UCSF’s Broad Center, has shown that some small RNA molecules called microRNAs promote adult cell “de-differentiation” and others promote the reverse: ability of stem cells to differentiate into adult cells. By tweaking microRNA activity, his lab has been able to improve reprogramming yields a hundred-fold.

He and colleagues have also become intrigued by the role of so-called epigenetic factors – naturally occurring or introduced molecules that modify proteins in the nucleus. Manipulation of these molecules too can affect the efficiency of inducing pluripotent cells. 

The Promise of Treatments

Six years after Yamanaka’s iPSCs discovery, researchers in a very different field developed a new gene-editing technology of unprecedented speed and precision, known as CRISPR-Cas9. The potent new tool has revolutionized efforts to “cut and paste” genes and has been very quickly adopted by thousands of researchers in basic biology and drug development.

“CRISPR has provided us with an extraordinary new capability,” Kriegstein says. “It allows us to tease apart the genetic causes or contributors to developmental diseases. We can edit out mutations to determine if they are critical to early developmental defects.”

CRISPR’s speed and precision may some day allow stem cell researchers to reach their most ambitious goal: Genetically abnormal cells from patients with inherited diseases such as sickle cell anemia or Huntington’s could be reprogrammed to the pluripotent stem cell state; their genetic defects could be “edited” in a petri dish before being differentiated into healthy adult cells. These cells could then be transplanted into patients to restore normal function.

iPSC-derived neurons generated from tissue taken from human patients with Huntington's Disease
These iPSC-derived neurons were generated from tissue taken from human patients with Huntington's Disease. The hope for the future is that abnormal cells from patients with inherited diseases such as Huntington’s could be reprogrammed to the pluripotent stem cell state, "edited" using CRISPR and then transplanted into patients to restore normal function. Photo by Julia Kaye/Gladstone Institutes

While that goal is still beyond reach, many early-stage clinical trials are underway using induced iPSCs to treat diseases, from diabetes and heart disease to Parkinson’s.

One trial has already treated its first patient. In 2014, Japanese scientists made iPSCs from skin cells of a woman with macular degeneration and then differentiated them into adult retinal cells. Surgeons transplanted the retinal cells into her eyes in order to treat the disease – the first patient treated using iPSCs.

Researchers focused on the eye disease in part because differentiating stem cells into retinal cells has proven to be fairly straightforward compared to many other cell types, Kriegstein says. Also, it is relatively easy to transplant cells into the eye.

Preparations to treat a second patient using patient-derived cells were stopped because the researchers detected a mutation in one of the genes in the iPS cells. No reports had linked the gene to cancer, but they decided not to use the stem cells to eliminate any risk.

The success of treatments relies in part on stem cells’ rapid rate of proliferation. Hundreds of billions of cells may sometimes be needed for a transplantation. But if just a few of the stem cells fail to differentiate into the target adult cells, they may reproduce rampantly when transplanted and form a tumor.

“It’s a two-edged sword,” says Yamanaka. “In the pre-transplant stage, you want stem cells that proliferate very rapidly. But after the transplant, if there are only five or 10 cells that didn’t differentiate into adult cells, they can reproduce infinitely. They create a kind of residue of tumor.”

Research to ensure that all stem cells differentiate before transplantation is now one of the main issues in this field, he says.

To eliminate cancer risk, the researchers are now “deep sequencing” the genetic makeup of each of the stem cell lines they might use. They have also decided to use donor cell lines rather than the patient’s own cells. This avoids the very expensive prospect of having to carry out quality checks like deep sequencing of each patient’s own pluripotent cell lines.

Use in Drug Screening

Cardiomyocytes reprogrammed from normal adult human skin samples
These cardiomyocytes were reprogrammed from normal adult human skin samples. Photo by Matt Spindler/Gladstone Institutes

The promise of treatment related to stem cells includes the promise of drug testing in adult human iPSC-derived cells rather than using animal models.

One recent example is the work of Catherine Mummery, a neurologist at Great Britain’s National Hospital for Neurology and Neurosurgery, who used iPSC-derived adult human cardiomyocytes – heart cells that will beat in a petri dish – to test two different commercially available drugs for cardiovascular disease. She showed that each drug triggered the same kind of therapeutic effect at one dose and the same type of toxicity at another dose that had been found in patients.

“This was impressive,” Kriegstein says. “It was an early proof-of-principle that drug testing in iPSC-derived adult human cells, rather than in animal models, can provide reliable results – and results that are more directly relevant to patients. Drug companies are starting to screen drugs in iPSC-derived human cells and organs.”

Other Sources, Old and New

Research using stem cells isn’t limited to IPSCs. In some respects, embryonic stem cells (ESCs) remain the gold standard. UCSF stem cell biologist Susan Fisher, PhD, sees early-stage ESCs as a blank slate.

“They have less of a history than iPS cells. They carry less baggage,” she says. But like Yamanaka and Kriegstein, she considers the field too young to declare the superiority of one strategy over the other.

A strong endorsement for tapping ESCs in transplantation medicine came two years ago when a Harvard team showed that cell lines derived from embryonic stem cells could produce unlimited supplies of insulin-producing islet cells. Early stage clinical trials are now underway, testing the safety and efficiency of transplanting islet cells into patients to treat type 1 diabetes.

As of 2014, hundreds of clinical trials are underway in many countries, primarily testing safety and efficacy of treatments for diseases, from heart failure to Parkinson’s.

The two well-known strategies to derive stem cells have recently been joined by a third, called direct cellular reprogramming or transdifferentiation. In this method, skin cells are turned directly into cells of the desired organ – brain, heart, pancreas – without first being drawn all the way back to a fully pluripotent stem cell stage. As a result, the method skirts the cancer risk inherent in differentiating truly pluripotent cells.

This year, Deepak Srivastava, MD – director of cardiovascular and stem cell research at the Gladstone Institutes and a professor of Pediatrics and of Biochemistry and Biophysics at UCSF – and a team led by Gladstone’s Ding efficiently transformed mouse skin cells into brain cells as well as beating heart cells using a combination of chemicals. The approach could prove effective in efforts to regenerate dying or diseased cells and tissues, Ding says.

Ethics and Public Perception

As the science progresses on many fronts, Yamanaka has become concerned that the science has gotten far ahead of efforts to consider the ethics of some of the research.

“When we made iPS cells, our purpose was to overcome ethical issues of embryonic stem cells. Now we are creating new ethical questions," Yamanaka says. "We can now make sperm or eggs from iPS cells, at least in mice. We may be able to make human organs in pigs and other animals by injecting human iPS cells into animal embryos– creating so-called chimeras.

The speed of scientific progress is getting faster and faster, so if we discuss the ethical issues slowly ... this is a big concern. Some think it’s science fiction. But it’s not for the future. It’s for ourselves.

Shinya Yamanaka, MD, PhD

“The speed of scientific progress is getting faster and faster, so if we discuss the ethical issues slowly ... this is a big concern. I have been asking many bioethicists to think about these issues more aggressively. Some think it’s science fiction. But it’s not for the future. It’s for ourselves.”

At the same time, he is concerned too about public perception that the rate of progress may be slower than expected.

“I am fascinated by how rapidly science is advancing. It’s amazing. But for the most part, developing new treatments – doing the science, testing the safety and effectiveness of new therapies­ – takes a great deal of money and many years,” Yamanaka said.

“Developing new treatments may take 10 years, 20 years, 30 years. That is what we have been trying to say to our patients: ‘We are making great progress, so do keep up your hope. But it takes time.’”