Tech
Jennifer Lewis ScD ’91: “Can we make tissues that are made from you, for you?”
“Can we make tissues that are made from you, for you?” asked Jennifer Lewis ScD ’91 at the 2025 Mildred S. Dresselhaus Lecture, organized by MIT.nano, on Nov. 3. “The grand challenge goal is to create these tissues for therapeutic use and, ultimately, at the whole organ scale.”
Lewis, the Hansjörg Wyss Professor of Biologically Inspired Engineering at Harvard University, is pursuing that challenge through advances in 3D printing. In her talk presented to a combined in-person and virtual audience of over 500 attendees, Lewis shared work from her lab that focuses on enhanced function in 3D printed components for use in soft electronics, robotics, and life sciences.
“How you make a material affects its structure, and it affects its properties,” said Lewis. “This perspective was a light bulb moment for me, to think about 3D printing beyond just prototyping and making shapes, but really being able to control local composition, structure, and properties across multiple scales.”
A trained materials scientist, Lewis reflected on learning to speak the language of biologists when she joined Harvard to start her own lab focused on bioprinting and biological engineering. How does one compare particles and polymers to stem cells and extracellular matrices? A key commonality, she explained, is the need for a material that can be embedded and then erased, leaving behind open channels. To meet this need, Lewis’ lab developed new 3D printing methods, sophisticated printhead designs, and viscoelastic inks — meaning the ink can go back and forth between liquid and solid form.
Displaying a video of a moving robot octopus named Octobot, Lewis showed how her group engineered two sacrificial inks that change from fluid to solid upon either warming or cooling. The concept draws inspiration from nature — plants that dynamically change in response to touch, light, heat, and hydration. For Octobot, Lewis’ team used sacrificial ink and an embedded printing process that enables free-form printing in three dimensions, rather than layer-by-layer, to create a fully soft autonomous robot. An oscillating circuit in the center guides the fuel (hydrogen peroxide), making the arms move up and down as they inflate and deflate.
From robots to whole organ engineering
“How can we leverage shape morphing in tissue engineering?” asked Lewis. “Just like our blood continuously flows through our body, we could have continuous supply of healing.”
Lewis’ lab is now working on building human tissues, primarily cardiac, kidney, and cerebral tissue, using patient-specific cells. The motivation, Lewis explained, is not only the need for human organs for people with diseases, but the fact that receiving a donated organ means taking immunosuppressants the rest of your life. If, instead, the tissue could be made from your own cells, it would be a stronger match to your own body.
“Just like we did to engineer viscoelastic matrices for embedded printing of functional and structural materials,” said Lewis, “we can take stem cells and then use our sacrificial writing method to write in perfusable vasculature.” The process uses a technique Lewis calls SWIFT — sacrificial writing into functional tissue. Sharing lab results, Lewis showed how the stem cells, differentiated into cardiac building blocks, are initially beating individually, but after being packed into a tighter space that will support SWIFT, these building blocks fuse together and become one tissue that beats synchronously. Then, her team uses a gelatin ink that solidifies or liquefies with temperature changes to print the complex design of human vessels, flushing away the ink to leave behind open lumens. The channel remains open, mimicking a blood vessel network that could have fluid actively, continuously flowing through it. “Where we’re going is to expand this not only to different tissue types, but also building in mechanisms by which we can build multi-scale vasculature,” said Lewis.
Honoring Mildred S. Dresselhaus
In closing, Lewis reflected on Dresselhaus’ positive impact on her own career. “I want to dedicate this [talk] to Millie Dresselhaus,” said Lewis. She pointed to a quote by Millie: “The best thing about having a lady professor on campus is that it tells women students that they can do it, too.” Lewis, who arrived at MIT as a materials science and engineering graduate student in the late 1980s, a time when there were very few women with engineering doctorates, noted that “just seeing someone of her stature was really an inspiration for me. I thank her very much for all that she’s done, for her amazing inspiration both as a student, as a faculty member, and even now, today.”
After the lecture, Lewis was joined by Ritu Raman, the Eugene Bell Career Development Assistant Professor of Tissue Engineering in the MIT Department of Mechanical Engineering, for a question-and-answer session. Their discussion included ideas on 3D printing hardware and software, tissue repair and regeneration, and bioprinting in space.
“Both Mildred Dresselhaus and Jennifer Lewis have made incredible contributions to science and served as inspiring role models to many in the MIT community and beyond, including myself,” said Raman. “In my own career as a tissue engineer, the tools and techniques developed by Professor Lewis and her team have critically informed and enabled the research my lab is pursuing.”
This was the seventh Dresselhaus Lecture, named in honor of the late MIT Institute Professor Mildred Dresselhaus, known to many as the “Queen of Carbon Science.” The annual event honors a significant figure in science and engineering from anywhere in the world whose leadership and impact echo Dresselhaus’ life, accomplishments, and values.
“Professor Lewis exemplifies, in so many ways, the spirit of Millie Dresselhaus,” said MIT.nano Director Vladimir Bulović. “Millie’s groundbreaking work, indeed, is well known; and the groundbreaking work of Professor Lewis in 3D printing and bio-inspired materials continues that legacy.”
Tech
Top Design Within Reach Promo Codes for March 2026
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Tech
A Billionaire-Backed Startup Wants to Grow ‘Organ Sacks’ to Replace Animal Testing
As the Trump administration phases out the use of animal experimentation across the federal government, a biotech startup has a bold idea for an alternative to animal testing: nonsentient “organ sacks.”
Bay Area-based R3 Bio has been quietly pitching the idea to investors and in industry publications as a way to replace lab animals without the ethical issues that come with living organisms. That’s because these structures would contain all of the typical organs—except a brain, rendering them unable to think or feel pain. The company’s long-term goal, cofounder Alice Gilman says, is to make human versions that could be used as a source of tissues and organs for people who need them.
For Immortal Dragons, a Singapore-based longevity fund that’s invested in R3, the idea of replacement is a core strategy for human longevity. “We think replacement is probably better than repair when it comes to treating diseases or regulating the aging process in the human body,” says CEO Boyang Wang. “If we can create a nonsentient, headless bodyoid for a human being, that will be a great source of organs.”
For now, R3 is aiming to make monkey organ sacks. “The benefit of using models that are more ethical and are exclusively organ systems would be that testing can be meaningfully more scalable,” Gilman says. (R3’s name comes from the philosophy in animal research known as the three R’s—replacement, reduction, and refinement—developed by British scientists William Russell and Rex Burch in 1959 to promote humane experimentation.)
New drugs are often tested in monkeys before they’re given to human participants in clinical trials. For instance, monkeys were critical during the Covid-19 pandemic for testing vaccines and therapeutics. But they’re also an expensive resource, and their numbers are dwindling in the US after China banned the export of nonhuman primates in 2020.
Animal rights activists have long pushed to end research on monkeys, and one of the seven federally funded primate research facilities across the country has signaled it would consider shutting down and transitioning into a sanctuary amid growing pressure. The US Centers for Disease Control and Prevention is also winding down monkey research, part of a bigger trend across the government to reduce reliance on animal testing.
As a result, Gilman says, there aren’t enough research monkeys left in the US to allow for necessary research if another pandemic threat emerges. Enter organ sacks.
Organ sacks would in theory offer advantages over existing organs-on-chips or tissue models, which lack the full complexity of whole organs, including blood vessels.
Gilman says it’s already possible to create mouse organ sacks that lack a brain, though she and cofounder John Schloendorn deny that R3 has made them. (For the record, Gilman doesn’t like the term “brainless” to describe the organ sacks. “It’s not missing anything, because we design it to only have the things we want,” she says.) Gilman and Schloendorn would not say how exactly they plan to create the monkey and human organ sacks, but said they are exploring a combination of stem-cell technology and gene editing.
It’s plausible that organ sacks could be grown from induced pluripotent stem cells, says Paul Knoepfler, a stem cell biologist at the University of California, Davis. These stem cells come from adult skin cells and are reprogrammed to an embryonic-like state. They have the potential to form into any cell or tissue in the body and have been used to create embryo-like structures that resemble the real thing. By editing these stem cells, scientists could disable genes needed for brain development. The resulting embryo could then be incubated until it grows into organized organ structures.
Tech
A Mysterious Numbers Station Is Broadcasting Through the Iran War
“Tavajoh! Tavajoh! Tavajoh!” a man’s voice announces, before going on to narrate a string of numbers in no apparent order, slowly and rhythmically. After nearly two hours, the calls of “Attention!” in Persian stop, only to resume again hours later.
The broadcast has been playing twice a day on a shortwave frequency since the start of the US-Israel attack on Iran on February 28.
According to Priyom, an organization which tracks and analyses global military and intelligence use of shortwave radio, using established radio-location techniques, the broadcast was first heard as the US bombing of Iran began. It has since played on the 7910 kHz shortwave frequency like clockwork—at 02.00 UTC and again at 18.00 UTC.
Over the weekend, Priyom said it had identified the likely origin of the broadcast. Using multilateration and triangulation techniques, the group traced the signal to a shortwave transmission facility inside a US military base in Böblingen, southwest of Stuttgart, Germany.
The site lies within a restricted training area between Panzer Kaserne and Patch Barracks, with technical operations possibly linked to the US army’s 52nd Strategic Signal Battalion, headquartered nearby.
That identification narrows the field, but it does not reveal who is behind the transmissions or who they are meant for.
The two-hour-long transmission is divided into five to six segments, each lasting up to 20 minutes. Each opens with “Tavajoh!” before shifting into a string of numbers in Persian, sometimes punctuated with an English word or two. Five days into the broadcast, radio jammers were heard attempting to block the frequency. The following day, the transmission shifted to a different frequency—7842 kHz.
Radio communication experts believe the broadcast is likely part of a Cold War–era system known as number stations.
The Return of the Numbers
Number stations are shortwave radio broadcasts that play strings of numbers or codes that sound random—like the one now heard in Iran. “It is an encrypted radio message used by foreign intelligence services, often as part of a complex operation by intelligence agencies and militaries,” says Maris Goldmanis, a Latvian historian and avid numbers stations researcher.
Number stations are most commonly associated with espionage. “For intelligence agencies, it is important to communicate with their spies to gather intelligence,” says John Sipher, a former US intelligence officer who served 28 years in the CIA’s National Clandestine Service. “This is not always possible in person due to political constraints or conflict. This is where number stations come in.”
While the use of number stations can be traced back to the First World War, they gained prominence during the US-Soviet Cold War. As espionage grew more sophisticated, governments used automated voice transmissions of coded numbers to communicate with agents, Goldmanis says. Citing declassified KGB and CIA documents, he adds that number stations were widely used during this period, often as Morse code transmissions and, in many cases, as two-way communications, with agents reporting back using their own shortwave transmitters.
“Nowadays, you have various satellite and encrypted communications technologies,” Sipher says. “But during the Cold War and even before that, governments had to find ways to do this without being noticed, and broadcasting coded messages was one way to communicate with your assets discreetly.”
The apparent randomness of the numbers means they can be understood only with a codebook, Sipher adds. “Nobody can make heads or tails of it or understand what it says unless you have the codebook that can give you hints to decrypt the code,” he says, noting that such systems must be set up and coordinated in advance.
A Signal Without a Sender
While the likely origin of the signal may now be clearer, its purpose and intended recipient remain unknown.
Because the broadcasts are encrypted and designed to be covert, those details may remain unclear for years, Goldmanis says. The structured nature of the transmission—its fixed schedule and consistent use of frequencies—further suggests it is part of a planned operation.
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