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CDR Dr. Jean-Paul Chretien — DARPA BTO — Regeneration, Resuscitation And Biothreat Countermeasures

Regeneration, Resuscitation & Biothreat Countermeasures — Commander Dr. Jean-Paul Chretien, MD, Ph.D., Program Manager, Biological Technology Office, DARPA


Commander Dr. Jean-Paul Chretien, MD, Ph.D. (https://www.darpa.mil/staff/cdr-jean-paul-chretien) is a Program Manager in the Biological Technology Office at DARPA, where his research interests include disease and injury prevention, operational medicine, and biothreat countermeasures. He is also responsible for running the DARPA Triage Challenge (https://triagechallenge.darpa.mil/).

Prior to coming to DARPA, CDR Dr. Chretien led the Pandemic Warning Team at the Defense Intelligence Agency’s National Center for Medical Intelligence, and as a naval medical officer, his previous assignments include senior policy advisor for biodefense in the White House Office of Science and Technology Policy; team lead for Innovation & Evaluation at the Armed Forces Health Surveillance Branch; and director of force health protection for U.S. and NATO forces in southwestern Afghanistan.

A proud mentor to nine graduate students and Oak Ridge Institute for Science and Education (ORISE) fellows, CDR Dr. Chretien received the Rising Star Award from the American College of Preventive Medicine, Best Publication of the Year Award from the International Society for Disease Surveillance, and Skelton Award for Public Service from the Harry S. Truman Scholarship Foundation. He has published over 50 peer-reviewed journal articles and 10 book chapters.

CDR Dr. Chretien earned a Bachelor of Science degree in political science from the United States Naval Academy, Master of Health Science in biostatistics and Doctor of Philosophy in genetic epidemiology degrees from the Johns Hopkins Bloomberg School of Public Health, and a Doctor of Medicine degree from the Johns Hopkins University School of Medicine. He completed his residency in general preventive medicine at the Walter Reed Army Institute of Research and fellowship in health sciences informatics at the Johns Hopkins University School of Medicine.

Organoid intelligence (OI): the new frontier in biocomputing and intelligence-in-a-dish

Recent advances in human stem cell-derived brain organoids promise to replicate critical molecular and cellular aspects of learning and memory and possibly aspects of cognition in vitro. Coining the term “organoid intelligence” (OI) to encompass these developments, we present a collaborative program to implement the vision of a multidisciplinary field of OI. This aims to establish OI as a form of genuine biological computing that harnesses brain organoids using scientific and bioengineering advances in an ethically responsible manner. Standardized, 3D, myelinated brain organoids can now be produced with high cell density and enriched levels of glial cells and gene expression critical for learning. Integrated microfluidic perfusion systems can support scalable and durable culturing, and spatiotemporal chemical signaling.

AI accurately identifies normal and abnormal chest X-rays

An artificial intelligence (AI) tool can accurately identify normal and abnormal chest X-rays in a clinical setting, according to a study published in Radiology.

Chest X-rays are used to diagnose a wide variety of conditions to do with the heart and lungs. An abnormal chest X-ray can be an indication of a range of conditions, including cancer and chronic lung diseases.

An AI tool that can accurately differentiate between normal and abnormal chest X-rays would greatly alleviate the heavy workload experienced by globally.

Modifying messenger RNA may provide a new target for Alzheimer’s disease

Reducing the methylation of a key messenger RNA can promote migration of macrophages into the brain and ameliorate symptoms of Alzheimer’s disease in a mouse model, according to a new study publishing March 7 in the open access journal PLOS Biology by Rui Zhang of Air Force Medical University in Xian, Shaanxi, China. The results illuminate one pathway for entrance of peripheral immune cells into the brain, and may provide a new target for treatment of Alzheimer’s disease.

A presumed trigger for the development of Alzheimer’s disease is the accumulation of proteinaceous, extracellular amyloid-beta plaques in the brain. High levels of amyloid-beta in mice leads to neurodegeneration and cognitive symptoms reminiscent of human Alzheimer’s disease, and reduction of amyloid-beta is a major goal in development of new treatments.

One potential pathway for getting rid of amyloid-beta is the of blood-derived into the brain, and their maturation into macrophages, which, along with resident microglia, can consume amyloid-beta. That migration is a complex phenomenon controlled by multiple interacting players, but a potentially important one is the methylation of messenger RNA within the cells.

How high altitude changes your body’s metabolism

Compared to those of us who live at sea level, the 2 million people worldwide who live above 4,500 meters (or 14,764 feet) of elevation—about the height of Mount Rainier, Mount Whitney, and many Colorado and Alaska peaks—have lower rates of metabolic diseases such as diabetes, coronary artery disease, hypercholesterolemia, and obesity.

Now, researchers at Gladstone Institutes have shed light on this phenomenon. They showed how chronically , such as those experienced at , rewire how mice burn sugars and fats. The work, published in the journal Cell Metabolism, not only helps explain the metabolic differences of people who live at high altitude, but could also lead to new treatments for metabolic disease.

“When an organism is exposed to chronically low levels of , we found that different organs reshuffle their fuel sources and their energy-producing pathways in various ways,” says Gladstone Assistant Investigator Isha Jain, Ph.D., senior author of the new study. “We hope these findings will help us identify metabolic switches that might be beneficial for metabolism even outside of low-oxygen environments.”

Null result in nicotinamide (vitamin B3) skin cancer trial of organ-transplant recipients

A one-year, placebo-controlled trial of oral nicotinamide (vitamin B3) therapy by the University of Sydney did not lead to lower rates of skin cancer in organ transplant recipients. The result is in striking contrast to a previous trial in which oral nicotinamide was concluded to be effective in reducing the rates of new nonmelanoma skin cancers and actinic keratoses in high-risk patients.

In the previous trial, “A Phase 3 Randomized Trial of Nicotinamide for Skin-Cancer Chemoprevention,” participants were ineligible if they were immunosuppressed. Results showed an estimated 23% lower overall rate of new nonmelanoma skin cancers, with similar reductions of both new basal-cell and squamous-cell carcinomas. Interestingly, the previous trial found five rare, more aggressive carcinomas (two morphoeic, three poorly differentiated) in the nicotinamide group, while the placebo control had zero.

Transplant recipients are commonly given immunosuppressant drugs to prevent the body’s immune system from attacking the new organ tissues. These patients are approximately 100 times more likely than the to develop , according to a Swedish study. A higher risk of developing combined with lower survival rates means transplant patients urgently need a safe and effective way to lessen the risk.

A wearable device that records single-neuron activity while humans are walking

New technologies can greatly advance research in various fields, including medicine and neuroscience. In recent years, for instance, engineers have created increasingly sophisticated devices to record brain activity and other biological signals with high precision.

A multi-disciplinary research team at University of California, Los Angeles (UCLA) and other institutes in the U.S. have recently developed the Neuro-stack, a new wearable technology that can record the activity of single neurons in the as a human being is walking or moving. This device, presented in a paper published in Nature Neuroscience, could help to gather valuable insight about neuronal activity during walking, while also potentially improving treatments for brain disorders.

“Our study was motivated by the need for smaller size and more for clinical neuroscience,” Dejan Markovic, one of the researchers who carried out the study, told Medical Xpress. “Our primary objectives were to make a device that is small enough to be wearable, for mobile experiments, and to provide broadband recordings including local field potentials and single units.”

Brain Criticality — Optimizing Neural Computations

To try everything Brilliant has to offer—free—for a full 30 days, visit http://brilliant.org/ArtemKirsanov/.
The first 200 of you will get 20% off Brilliant’s annual premium subscription.

My name is Artem, I’m a computational neuroscience student and researcher. In this video we talk about the concept of critical point – how the brain might optimize information processing by hovering near a phase transition.

Patreon: https://www.patreon.com/artemkirsanov.
Twitter: https://twitter.com/ArtemKRSV

OUTLINE:
00:00 Introduction.
01:11 — Phase transitions in nature.
05:05 — The Ising Model.
09:33 — Correlation length and long-range communication.
13:14 — Scale-free properties and power laws.
20:20 — Neuronal avalanches.
25:00 — The branching model.
31:05 — Optimizing information transmission.
34:06 — Brilliant.org.
35:41 — Recap and outro.

The book: https://mitpress.mit.edu/9780262544030/the-cortex-and-the-critical-point/

REFERENCES (in no particular order):

“Organoid Intelligence” — Revolutionary Biocomputers Powered by Human Brain Cells

Despite AI’s impressive track record, its computational power pales in comparison with a human brain. Now, scientists unveil a revolutionary path to drive computing forward: organoid intelligence, where lab-grown brain organoids act as biological hardware.

Artificial intelligence (AI) has long been inspired by the human brain. This approach proved highly successful: AI boasts impressive achievements – from diagnosing medical conditions to composing poetry. Still, the original model continues to outperform machines in many ways. This is why, for example, we can ‘prove our humanity’ with trivial image tests online. What if instead of trying to make AI more brain-like, we went straight to the source?

Scientists across multiple disciplines are working to create revolutionary biocomputers where three-dimensional cultures of brain cells, called brain organoids, serve as biological hardware. They describe their roadmap for realizing this vision in the journal Frontiers in Science.