Lifeboat Foundation

NASA’s James Webb Space Telescope has unveiled a stunning 3D visualization of 5,000 galaxies, providing a glimpse into the vast cosmic expanse.

The visualization, part of the Cosmic Evolution Early Release Science (CEERS) Survey, takes viewers on a journey through nearby galaxies to those in the far reaches of the universe, including one that has never been seen before by the telescope.

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SAN FRANCISCO, July 11 (Reuters) — International Business Machines (IBM) (IBM.N) is considering the use of artificial intelligence chips that it designed in-house to lower the costs of operating a cloud computing service it made widely available this week, an executive said Tuesday.

In an interview with Reuters at a semiconductor conference in San Francisco, Mukesh Khare, general manager of IBM Semiconductors, said the company is contemplating using a chip called the Artificial Intelligence Unit as part of its new “watsonx” cloud service.

IBM is hoping to take advantage of the boom in generative AI technologies that can write human-like text more than a decade after Watson, its first major AI system, failed to gain market traction.

AI is growing in its capability, and threatens the way we live and our security. Other technologies like Web3/metaverse and defi are not as threatening, and are shrinking in importance as interest rates rise.

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Autophagy plays important but complex roles in aging, affecting health and longevity. We found that, in the general population, the levels of ATG4B and ATG4D decreased during aging, yet they are upregulated in centenarians, suggesting that overexpression of ATG4 members could be positive for healthspan and lifespan. We therefore analyzed the effect of overexpressing Atg4b (a homolog of human ATG4D) in Drosophila, and found that, indeed, Atg4b overexpression increased resistance to oxidative stress, desiccation stress and fitness as measured by climbing ability. The overexpression induced since mid-life increased lifespan. Transcriptome analysis of Drosophila subjected to desiccation stress revealed that Atg4b overexpression increased stress response pathways. In addition, overexpression of ATG4B delayed cellular senescence, and improved cell proliferation.

There’s a bouncer in everyone: The blood-brain barrier, a layer of cells between blood vessels and the rest of the brain, kicks out toxins, pathogens and other undesirables that can sabotage the brain’s precious gray matter.

When the bouncer is off its guard and a rowdy element gains entry, a variety of conditions can crop up. Barrier-invading cancer cells can develop into tumors, and multiple sclerosis can occur when too many white blood cells slip pass the barrier, leading to an autoimmune attack on the protective layer of brain nerves, hindering their communication with the rest of the body.

“A leaky blood-brain barrier is a common pathway for a lot of brain diseases, so to be able to seal off the barrier has been a long sought-after goal in medicine,” said Calvin Kuo, MD, PhD, the Maureen Lyles D’Ambrogio Professor and a professor of hematology.

Cedars-Sinai investigators have identified several steps in a cellular process responsible for triggering one of the body’s important inflammatory responses. Their findings, published in the journal Science Immunology, open up possibilities for modulating the type of inflammation associated with several infections and inflammatory diseases.

Specifically, the investigators have improved understanding of the steps that lead to the production of IL-1 beta, a potent inflammatory protein signal released during many inflammatory responses.

“We now have a clearer understanding of the stepwise process that leads to the production of IL-1 beta,” said Andrea Wolf, Ph.D., assistant professor of Biomedical Sciences and Medicine at Cedars-Sinai, and a senior and corresponding author on the new study. “By understanding the process, we hope to one day find a treatment for diseases associated with this inflammatory response.”

Learn about the heart and and how it works from WebMD.

A rare, half-billion-year-old fossil gives us a clue to how a bizarre marine invertebrate can possibly be related to humans. In a study published on July 6 in the journal Nature Communications, Harvard University researchers identified a prehistoric specimen in a collection at the Natural History Museum of Utah as a tunicate, or sea squirt. The preserved invertebrate, which was originally discovered in the rugged, desert-like landscape of the House Range in western Utah, can be used to understand evolution mysteries that go way back to the Cambrian explosion.

“There are essentially no tunicate fossils in the entire fossil record. They’ve got a 520-to 540-million year-long gap,” says Karma Nanglu, an invertebrate paleontologist at Harvard. “This fossil isthe first soft-tissue tunicate in, we would argue, the entire fossil record.”

Sea squirts can be seen swaying on the ocean floor with its potato-like body and two chimney-like parts called siphons that are used to feed and expel water. While there are at least 3,000 different species today, the crayon-point-size organisms are generally unknown to people—despite being our invertebrate cousins, says Nanglu. Like humans, they belong to the chordates, which share five essential physical features during development or when fully grown. Most tunicates hatch as swimming, tadpole-like creatures, but eventually attach to the ocean floor and lead a sessile lifestyle.