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In a First, a Scientist Regrew a Human Lung in a Bioreactor. Is This the Dawn of Rebuilding Humans Piece by Piece?
Stav Dimitropoulos · 2026-06-27 · via Latest Content - Popular Mechanics

Around 2010, Michael Riddle was a broke medical student in his late thirties supporting a wife and four children at the University of Texas Medical Branch (UTMB). One day, Riddle walked into a Galveston pet store and noticed a $20, three-and-a-half-gallon fish tank—not as a home for pets but because the tank looked remarkably like a human thoracic cavity to him. Riddle used it to build what he describes as the world’s first large lung bioreactor, a chamber designed to grow living lungs outside the body.

The device helped researchers grow engineered pig lungs that were transplanted into pigs, as well as what Riddle describes as the first human lung grown in a laboratory. He eventually sold the design to Harvard Apparatus, a laboratory equipment company in Massachusettes whose commercial version helped advance one of regenerative medicine’s biggest ambitions: growing replacement organs from a patient’s own cells. Today, Riddle is an MD and CEO of Mesogen, a Texas biotechnology company developing personalized cell therapies. His story has all the ingredients of a Hollywood underdog movie. At the same time, the technology he helped pioneer evokes eerie echoes of Mary Shelley’s Frankenstein—but with a hopeful twist. Instead of stitching together body parts from different people, scientists are attempting to rebuild the body using its own cells.

The idea behind the technology Riddle helped develop, alongside other lung bioengineering researchers at UTMB, is deceptively simple. First, the team decellularizes a donor lung that can no longer be used clinically, washing away its original cells while leaving behind a ghostly white biological scaffold—a complex framework of proteins and microscopic structures that still retains the organ’s shape. Then they recellularize it by adding cells from the intended recipient, hoping to transform an organ destined for medical waste disposal into a new, personalized replacement.

The concept has already worked in mice. While working in the UTMB laboratory, Riddle watched researchers routinely decellularize and recellularize mouse lungs. But when he asked why they weren’t scaling up the process to humans and large animals, he got two answers: “It takes us five months to decellularize a large pig lung,” and “There’s no bioreactor big enough to grow a lung.”

But then came a breakthrough from an unexpected quirk of anatomy: lungs float in any liquid. “There’s no way to get all the air out of a lung,” Riddle says. At first, he saw that as an impediment and tried squeezing the air out, but without success.

“It’s going to float no matter what I try to do,” he thought. “So I decided to use that to my advantage.”

Instead of fighting buoyancy, Riddle turned the pig lung upside down and attached the trachea, the body’s main airway, to a pipe at the bottom of the tank. This allowed the organ to remain suspended without compressing its delicate blood vessels. He then pumped a detergent solution through the lung’s blood vessels and its airways simultaneously. According to Riddle, the approach reduced the time needed to decellularize a pig lung from roughly five months to just three days.

Researchers at UTMB later transplanted engineered lungs into pigs. The rebuilt lungs integrated with the animals’ bodies and continued to mature for up to two months without signs of rejection or major complications, although they were not yet capable of functioning as the pigs' sole lungs. The team also went on to grow what it described as the first human lung in a laboratory using a biological scaffold and stem cells. Together, the work showed that researchers could strip human-sized lungs of their original cells, repopulate them with new ones, and grow them outside the body.

But why go through all this trouble to grow a lung in the first place?

The answer lies in the dire and chronic shortage of donor organs. In the United States alone, more than 100,000 people are waiting for a transplant at any given time. Meanwhile, only about 20 to 30 percent of donated lungs ever make it into a patient.

“A lot of lungs that are harvested for transplant time out because they couldn’t find a donor quickly enough, or there was something about that lung that made it unsuitable for transplant,” Riddle says. “So there are many, many lungs—and other tissue for that matter—that end up getting thrown away.”

The premise behind lung bioengineering is to rescue some of those discarded organs through decellularization and recellularization. But the approach offers another potential advantage.

Conventional organ recipients receive allogeneic organs, which are from other people. That typically requires lifelong immunosuppressive drugs because the immune system is remarkably good at distinguishing “self” from “not self.” Without those drugs, your body may rapidly recognize the transplanted organ as foreign tissue and attack it. The tradeoff is steep: while immunosuppression protects the transplanted organ, it also leaves patients more vulnerable to infections and weakens one of the body’s natural defenses against emerging cancer cells. Researchers hope that rebuilding organs from a patient’s own cells will sidestep that problem altogether.

“To make a safe treatment for a patient, the cells have to come from the patient,” says Riddle. Whether for lungs or newer projects (including experimental therapies for degenerative eye disease and Type 1 diabetes), the central idea remains the same: use the body’s own cells to rebuild what disease has ravaged.

The implications could extend well beyond organ transplants. If researchers can reliably grow human tissues and organs in the laboratory, they may eventually be able to test new drugs directly on living human organs rather than relying exclusively on animals or simplified laboratory models. A bioengineered lung, for example, could become a testing ground for experimental therapies long before they reach patients, helping researchers better predict which treatments will work, and which might fail.

As scientists pursue that future, they disagree on how best to get there. Some are trying to print or engineer complex organs from scratch. Others, including Riddle, believe the better approach begins with nature’s own designs.

His philosophy is clear: the closer scientists stay to nature’s original design, the better their chances of success. To illustrate his point, he references pioneering work by regenerative medicine researcher Doris Taylor, PhD, who led efforts at the Texas Heart Institute in the late 2000s to create bioengineered replacement hearts. The process stripped donor hearts of their cells and repopulated them with new ones. While the hearts beat in the laboratory, Riddle argues they never generated enough force to pump blood effectively in a body.

Regardless of where the debate over the best approach ultimately leads, researchers broadly agree that Riddle and his colleagues helped move lung bioengineering forward—even if transplant-ready lungs still lie over the horizon.

“The lung bioengineering work showed that human-scale lungs can be turned into cellular scaffolds and then partially repopulated with several human lung cell types in a dedicated lung bioreactor,” says Charlie Ren, PhD, an associate professor of biomedical engineering at Carnegie Mellon University.

However, Ren cautions that turning discarded lungs into transplant-ready replacement organs remains a long-term goal. Researchers still need to generate enough patient-specific cells, repopulate every part of the lung, achieve reliable gas exchange, and develop manufacturing methods that can work at scale, he says.

Even so, he believes the burgeoning technology of organ bioengineering could transform healthcare over the coming decades. It could increasingly emphasize repair and regeneration while enabling specialized manufacturing hubs to quietly grow the tissues and organs patients need, instead of waiting for tragedy to supply them.

Those hurdles are formidable. But Riddle believes they had better be tackled by working with biology rather than trying to outsmart it. He remains skeptical of efforts to build highly complex organs entirely from scratch, even when they come from what he calls “super smart” scientists. Existing biological structures, developmental processes, and a patient’s own cells, he argues, already provide the best starting point.

Who would have thought that more than two centuries after Shelley dreamed up her patchwork creature, the closest approximation to Frankenstein’s creation would begin not in a graveyard, but in an operating room—where organs destined for the trash might one day breathe life anew, provided scientists use only the very cells of the person they are meant to save?

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➡ The Race to Revolutionize EV Batteries

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Stav Dimitropoulos is a Gold and Community Anthem Award–winning journalist, and writes about consciousness, science, and culture for Popular Mechanics, Nature, and the BBC. Her work often explores mind-stretching angles where science meets philosophy. Her debut nonfiction book, Slow, Lazy, Gluttons (Greystone Books, 2026) asks: What if the traits society shames — laziness, darkness, nostalgia, and more — are actually survival superpowers?