This progress adds to the growing number of medical training programs replacing live animal use with ethical, effective, human-relevant simulation models.
See more from @pcrm.org
www.pcrm.org/ethical-scie...
Congratulations to the team at @pcrm.org, who worked with Rhode Island state legislators and physicians for years to make this change happen.
www.pcrm.org/news/news-re...
Brown University has ended the use of live animals for it’s emergency medicine residency program, bringing the number of U.S. #EmergencyMedicine residency programs using animals down to just 8️⃣.
www.browndailyherald.com/article/2026...
#MedSky #MedEd #EMedSky #Residency
By @tamu.bsky.social's Weijian Hua and Akhilesh K. Gaharwar
In @natureportfolio.nature.com's Biomedical Innovations: www.nature.com/articles/s44...
#bioegineering #biofabrication
"This work outlines the technological landscape and future directions for biofabrication in a post-animal testing era."
Don't miss this thorough new review on the role of #bioprinting in replacing the use of animals in biomedical research and testing.
#3Dprinting 🧪
These organoids offer a promising platform for long-term studies of neuronal development, retinal ganglion cell maturation, & connectivity, with the potential to model human retinal disease & test therapies.
Read in @cp-cellstemcell.bsky.social
www.cell.com/cell-stem-ce...
Graphical abstract from the linked Cell Stem Cell paper, "Retinal ganglion cell survival and functional maturation in transiently vascularized human retinal organoids," by Sharma et al. (10.1016/j.stem.2025.12.013).
At University Hospital Bonn & @iobswiss.bsky.social, @ruizdealmodovar.bsky.social, @tamvir.bsky.social, & colleagues created transiently vascularized human retinal #organoids with enhanced retinal ganglion cell survival & function.
#Ophthosky 🧪
💰
@volkswagenstiftung.de
@dfg.de
@erc.europa.eu
They discovered that rotational migration depends on myosin activity, actin polymerization, & actin branching, and suggest that this model can be used to investigate additional unresolved regulatory mechanisms underlying this process.
Read in @commsbio.nature.com
www.nature.com/articles/s42...
Figure 2 from "Rotational migration in human pancreatic ductal organoids depends on actin and myosin activity" by Xie et al. in Communications Biology. The title and caption for the figure read: "Trajectory and velocity of pancreatic ductal organoid rotation. A Overlay of maximum projections of a rotating pancreatic ductal organoid (organoid #1) taken every 30 minutes, between hours 3 and 7 of the live imaging. To illustrate the rotational migration of the cells, the nuclei were color-coded based on the time point they were imaged. The transparent green arrow indicates the general direction of the rotation. The X and Y position coordinates start from the top left of the image. Bar = 50 µm. B Three-dimensional reconstruction of the nuclei trajectories within the rotating organoid #1. C Vector plot showing the direction and the velocity of nuclei displacement between each time point. The length of the arrows is scaled to the velocity of the nucleus. The vector plot is projected to the XY axis to illustrate the rotational migration of organoid #1. D The nuclei average velocity remains relatively stable at ~12–22 µm/hr over the imaging period (mean ± SEM, N = 3 organoids from three independent experiments, n = 21–48 nuclei per organoid from 7 hours of imaging period, i.e., 15 time points). E Histogram plot showing the distribution of the recorded velocity. The velocity ranges between 0 and 35 µm/hr, with peaks at ~15–20 µm/hr (N = 3 organoids from three independent experiments, n = 21–48 nuclei per organoid from 7 hours of imaging period, i.e., 15 time points). F Average velocity of three independent pancreatic ductal organoids, showing a range between ~15 and ~18 µm/hr (mean ± SD, N = 3 organoids from three independent experiments, n = 21–48 nuclei per organoid from 7 hours of imaging period, i.e., 15 time points)."
Using human pancreatic ductal #organoids, @utaustin.bsky.social scientists studied collective migration of epithelial cells, which plays a role in morphogenesis, wound repair, tissue homeostasis, & cancer metastasis. 🧪
Funded by @amdiabetesassn.bsky.social, @thewelchfoundation.bsky.social, et al.
We're raising the visibility of #WomensHealth in @apspublications! Explore #CallsForPapers on key women’s health research topics & submit your study journals.physiology....
#Alzheimers #AutoimmuneDiseases #BreastCancer #CVDisease #Menopause #Migraines #Pregnancy #Endometriosis #Preeclampsia
This non-animal liver model also:
✅ Is compatible with the Fundamentals of Laparoscopic Surgery (FLS) trainer for minimally invasive repair practice ✅ Can be filled with a red fluid mixture and lacerated
✅ Supports team-based scenarios managing actively hemorrhaging liver injuries
On the other hand, this new model is:
🟢 Reusable and cost-effective
🟢 Constructed from standard simulation center materials 🟢 Free from the ethical concerns of animal use
🟢 Practical and scalable for training programs
The authors highlight these problems w using animal tissues for medical training:
🔸 Cost, due to time-demanding collection
🔸 Risk of disease transmission & environmental hazards during shipping/handling
🔸 Rapid spoilage, requiring new purchases for every cohort
🔸 Ethical & cultural concerns
Screenshot from the linked webpage, showing the following article title and author information: "Construction of an Animal-Alternative Liver Model for Surgical Simulation Training" October 29, 2025. Authors: Brian F. Quach BS; Alexander Hayden MS, PA-C; Eric Nohelty BS, CHSOS; Andrew J. Eyre MD, MS; Frank H. Netter MD School of Medicine at Quinnipiac University, North Haven, CT; William W. Backus Hospital, Department of Surgery, Norwich, CT; STRATUS Center for Medical Simulation, Boston, MA; Brigham and Women’s Hospital, Department of Emergency Medicine, Boston, MA; Harvard Medical School, Boston, MA"
This sustainable, reusable liver model for surgical skills training was built entirely from materials already found in a simulation lab.
Read in @healthcaresim.bsky.social ⬇️
www.ssih.org/news/constru...
🏥 @stratusbwh.bsky.social @harvardmed.bsky.social
#MedSky #MedEd #SurgSky #SurgEd #Simulation
“For years, it’s always been thought that animals should be the default,” Valerie Speirs told @dianakwon.bsky.social for @nature.com
🔗 www.nature.com/articles/d41...
Scientists are frustrated by slow progress & feel that papers & grant applications are still expected to include animal experiments.
Meme from the 2004 movie Mean Girls, picturing Rachel McAdams as Regina George wearing a Santa hat. The line from the movie, “Stop trying to make fetch happen” has been changed to “Stop trying to make mouse happen.”
Instead of meeting mouse experimenters halfway, human neuroscientists should bring them fully over, working together to modernize and humanize neuroscience in ways that have never possible before.
Direct recordings from awake humans are offering clinically relevant insights.
Advanced in vitro models of human brains are enabling unprecedented basic & applied neuroscience research.
Continuing to use mice distracts the field, produces misleading stories & consumes limited funding resources.
But neuroscience’s problem isn’t a lack of mouse–human integration; it’s reliance on mice at all.
Experiments on rodents keep generating theories that fail in or mislead humans (looking at you, amyloid hypothesis) because human brains evolved uniquely and mice & rats aren’t good stand-ins.
The problem is real.
While mice and humans share ~85% of protein-coding genes, the regulation of those genes is often remarkably different.
Imagine a piano: with the same keys you can play an infinite number of distinct songs.
For @thetransmitter.bsky.social, @suthanalab.bsky.social wrote about neuroscience's "species problem." www.thetransmitter.org/animal-model...
"[T]he field has largely compartmentalized the findings, enabling parallel literatures to proceed with little pressure to reconcile them."
#neuroskyence
Experiments on animals were a poor 'gold standard,' and we now have the tools to move beyond them.
So, let’s choose progress.
Add your name in support of Research Modernization NOW to help further the evolution to human-relevant science: www.scienceadvancement.org/open-letter-...
Screenshot from the article: "The increasing adoption of NAMs makes rigorous validation essential, says Kent Lloyd, a geneticist and director of the NAMs Testing Center at the University of California, Davis. “Unless we hold NAMs to the same level of rigour and transparency that we expect of animal models, there will be harm done,” he says."
But I'm struck by the article's focus on validation.
It's critical, of course, that any methods used to make decisions about human health are validated. However, the article assumes that experiments & tests on animals also underwent as strict a period of 'validation.'
They did not.
Screenshot from the article: "Take sepsis, for instance, a severe reaction to infection. Researchers have developed more than 100 therapies for sepsis that looked promising in rodent models but that were ineffective in clinical trials3. That’s partly because of differences in human and rodent immune systems and the difficulty of mimicking a complex condition that varies from one person to the next in inbred mice that are genetically similar and raised in uniform conditions."
Great to see #sepsis mentioned. Animal use has misled this field even more than most.
SAO report on sepsis: www.scienceadvancement.org/wp-content/u...
While you're here, please sign this open letter urging the U.K. to set clear goals for sepsis research: secure.peta.org.uk/page/179711/...
"The age of animal experiments is waning," writes @dianakwon.bsky.social for @nature.com
www.nature.com/articles/d41...
Kwon covers the recent policy changes in the U.S. & U.K. that give major boosts to the use & development of non-animal methodologies.
#NAMs #SciPol 🧪
ICYMI💡 My badass colleague @katherineroe.bsky.social sat down with Dr. Mia Wood, host of the @labroots.bsky.social podcast "The Life of Her Mind," to discuss what drives women scientists like her to challenge the status quo.
Give it a listen: www.labroots.com/podcast-seri...
"You can say, ‘Oh, it’s just public relations.’ Public relations matter."
Why would they remove 'Primate' from their name?
Maybe it's because the social license for AND the scientific necessity of experimenting on monkeys is at an all time low.
They see the writing on the wall.
He was a young baboon. Two days after entering a Columbia University laboratory, he was dead.
His death illustrates how the animal research oversight system does not exist to eliminate harm to animals. Rather, it expects harm and exists to manage it.
riseforanimals.org/news/baboon-...
#animalrights
The 3Rs don’t hold up when you become the subject.
Thought experiments and virtual scenarios like these are impactful because they expose a simple truth:
If we wouldn’t accept these experiments on humans, we shouldn’t accept them for other animals, who may not look or speak like we do, but suffer just the same.
#animalrights #bioethics
👽 What if you could step onto the spaceship yourself?
@peta2.bsky.social’s award‑winning VR Abduction drops students across the U.S. into a sci‑fi scenario where they become the test subjects—powerless, scared, and without consent, what animals in labs endure daily.
www.peta2.com/news/abducti...
The 3Rs are window dressing, not ethics.
Even those who use them admit their limits when the roles reverse.
They mask the deeper moral problems of using others as research tools.
Read more in this SAO Reflection by @katibertrand.bsky.social 👉 www.scienceadvancement.org/reflections/...
