Many coral reefs "have now turned ghostly white," reports CBS News — and "a major culprit is climate change."

SFGate adds that more than 50% of the world's coral reefs have been lost, mostly over the past 10 years, according to coral reef scientist Rebecca Albright at the California Academy of Sciences. "If changes aren't made soon, 90% to 99% of the coral reefs that are remaining could be deteriorated by 2050, Albright said..."

But CBS News notes that Albright's lab is the first in America to successfully spawn coral to regenerate the reefs: The lab is mastering the art and science of creating baby corals, and the scientists have brought their expertise into the wild. The location: the second-largest reef in the world, known as the Mesoamerican Reef, stretching some 700 miles along the coasts of Mexico, Belize, Guatemala, and Honduras... Armed with test tubes, the scientists quickly dove into the water and collected the tiny packets of gametes. Back on land, the eggs were fertilized, incubated, and then brought back into the wild. "Then we planted over 3,000 baby corals back to the reef," explained Albright. The baby corals are now two months old. The Roatan staff will dive in a few months to see how many survived.
Scientists are worried because bleaching events "are becoming more common," notes SFGate, "happening more frequently and affecting more parts of the world... The most current event was confirmed on April 15, 2024, and is still ongoing, impacting approximately 84% of the world's coral reefs as of August 31.

"It has been documented in at least 83 countries and territories."

"In Boston labs, old, blind mice have regained their eyesight, developed smarter, younger brains and built healthier muscle and kidney tissue," reports CNN: On the flip side, young mice have prematurely aged, with devastating results to nearly every tissue in their bodies. The experiments show aging is a reversible process, capable of being driven "forwards and backwards at will," said anti-aging expert David Sinclair, a professor of genetics in the Blavatnik Institute at Harvard Medical School and codirector of the Paul F. Glenn Center for Biology of Aging Research. Our bodies hold a backup copy of our youth that can be triggered to regenerate, said Sinclair, the senior author of a new paper showcasing the work of his lab and international scientists.

The combined experiments, published for the first time Thursday in the journal Cell, challenge the scientific belief aging is the result of genetic mutations that undermine our DNA, creating a junkyard of damaged cellular tissue that can lead to deterioration, disease and death. "It's not junk, it's not damage that causes us to get old," said Sinclair, who described the work last year at Life Itself, a health and wellness event presented in partnership with CNN. "We believe it's a loss of information — a loss in the cell's ability to read its original DNA so it forgets how to function — in much the same way an old computer may develop corrupted software. I call it the information theory of aging."

Jae-Hyun Yang, a genetics research fellow in the Sinclair Lab who coauthored the paper, said he expects the findings "will transform the way we view the process of aging and the way we approach the treatment of diseases associated with aging."
While Sinclair is now testing "genetic resets" in primates, the article warns that "decades could pass before any anti-aging clinical trials in humans begin, get analyzed and, if safe and successful, scaled to the mass needed for federal approval."

But Sinclair suggests damage could probably also be repaired through healthy behaviors like exercise and sufficient sleep, social support and lower stress levels, eating less often and focusing on plants.

Thanks to long-time Slashdot reader 192_kbps for sharing the story.

MIT News: In the 1920s, German chemist Otto Warburg discovered that cancer cells don't metabolize sugar the same way that healthy cells usually do. Since then, scientists have tried to figure out why cancer cells use this alternative pathway, which is much less efficient. MIT biologists have now found a possible answer to this longstanding question. In a study appearing in Molecular Cell, they showed that this metabolic pathway, known as fermentation, helps cells to regenerate large quantities of a molecule called NAD+, which they need to synthesize DNA and other important molecules. Their findings also account for why other types of rapidly proliferating cells, such as immune cells, switch over to fermentation. "This has really been a hundred-year-old paradox that many people have tried to explain in different ways," says Matthew Vander Heiden, an associate professor of biology at MIT and associate director of MIT's Koch Institute for Integrative Cancer Research. "What we found is that under certain circumstances, cells need to do more of these electron transfer reactions, which require NAD+, in order to make molecules such as DNA." Vander Heiden is the senior author of the new study, and the lead authors are former MIT graduate student and postdoc Alba Luengo PhD '18 and graduate student Zhaoqi Li.

Fermentation is one way that cells can convert the energy found in sugar to ATP, a chemical that cells use to store energy for all of their needs. However, mammalian cells usually break down sugar using a process called aerobic respiration, which yields much more ATP. Cells typically switch over to fermentation only when they don't have enough oxygen available to perform aerobic respiration. Since Warburg's discovery, scientists have put forth many theories for why cancer cells switch to the inefficient fermentation pathway. Warburg originally proposed that cancer cells' mitochondria, where aerobic respiration occurs, might be damaged, but this turned out not to be the case. Other explanations have focused on the possible benefits of producing ATP in a different way, but none of these theories have gained widespread support. In this study, the MIT team decided to try to come up with a solution by asking what would happen if they suppressed cancer cells' ability to perform fermentation. To do that, they treated the cells with a drug that forces them to divert a molecule called pyruvate from the fermentation pathway into the aerobic respiration pathway.

An anonymous reader quotes a report from Scientific American about a device that delivers infusions of DNA and other molecules to restore injured limbs in mice, and maybe someday, humans: Cells are typically reprogrammed using mixtures of DNA, RNA and proteins. The most popular method uses viruses as a delivery vehicle -- although they can infect unintended cells, provoke immune responses and even turn cells cancerous. One alternative, called bulk electroporation, exposes cells to an electric field that pokes holes in their membranes to let in genetic material and proteins. Yet this method can stress or kill them. Tissue nanotransfection, described in a study published in August in Nature Nanotechnology, involves a chip containing an array of tiny channels that apply electric fields to individual cells. "You affect only a small area of the cell surface, compared with the conventional method, which upsets the entire cell," says study co-author James Lee, a chemical and biomolecular engineer at The Ohio State University. "Essentially we create a tiny hole and inject DNA right into the cell, so we can control the dosage."

Chandan Sen, a physiologist at Ohio State, and his colleagues developed a genetic cocktail that rapidly converts skin cells into endothelial cells -- the main component of blood vessels. They then used their technique on mice whose legs had been damaged by a severed artery that cut off blood supply. New blood vessels formed, blood flow increased, and after three weeks the legs had completely healed.

concertina226 writes Engineering students from the University of Toronto have developed a 3D bioprinter that can rapidly create artificial skin grafts from a patient's cells to help treat burn victims. In severe burn injuries, both the epidermis (outer layer of the skin) and the dermis (inner layer) are severely damaged, and it usually takes at least two weeks for skin cells to be grown in a laboratory to be grafted onto a patient. As both layers of skin are made from completely different cells that have different structures, it is very difficult for the body to regenerate itself and burn victims can die if their wounds cannot be closed quickly enough. So instead of trying to replicate a real human skin graft, the PrintAlive Bioprinter creates a type of "living bandage" from hydrogel.

Zothecula writes Muscle lost through traumatic injury, congenital defect, or tumor ablation may soon be regenerated from within. A team of researchers at Wake Forest Baptist Medical Center has shown how stem cells in the body of mice and rats can be mobilized to form new muscle in damaged regions. "Working to leverage the body’s own regenerative properties, we designed a muscle-specific scaffolding system that can actively participate in functional tissue regeneration," explains Sang Jin Lee, senior author on the study. This scaffold was implanted in the rats' tibialis anterior muscle (which is found below the knee), serving as a kind of home for the muscle progenitor cells to grow and develop.

An anonymous reader writes "Researchers have discovered a promising method to regrow damaged nerves in adults. Brain and spinal-cord injuries typically leave people with permanent impairment because the injured nerve fibers (axons) cannot regrow. A study from Harvard and Carleton University, published in the December 10 issue of the journal Neuron, shows that axons can regenerate vigorously in a mouse model when a gene that suppresses natural growth factors is deleted. Here is the journal article (subscription required to view more than the abstract)."

esocid tips us to news out of Duke University Medical Center, where researchers have discovered a type of microRNA that is related to the ability of zebrafish to regenerate lost or damaged organs. This is the result of a study initiated after it was discovered that zebrafish were able to recover from "massive injury" to the heart through their own regenerative biology. The scientists hope to be able to use this information to bring about similar healing in humans. Zebrafish have also been helpful in cancer research. "In zebrafish, one or more microRNAs appear to be important to keep regeneration on hold until the fish needs new tissue, the Duke researchers say. In response to an injury, the fish then damp down levels of these microRNAs to aid regrowth. Poss and many other cell biologists believe that mammals may have the same tissue regeneration capability as zebrafish, salamanders and newts, but that it is locked away somewhere in our genome, silenced in the course of evolution."

NewScientist reports that researchers have discovered stem cells in the heart, leading them to believe that the heart can regenerate itself. From the article: "The finding raises the possibility that these cardiac stem cells could one day be manipulated to rebuild tissues damaged by heart disease - still the leading cause of death in the US and UK. Because fully developed heart cells do not divide, experts have believed the organ was unable to regenerate after injury. But, in 2003, researchers at Piero Anversa's laboratory at New York Medical College in Valhalla, New York, US, discovered stem cells in the hearts of mice, and subsequently humans. However, they still did not know whether these stem cells actually resided in the heart or had merely migrated there from another tissue, such as bone marrow."