Feature Channels: Cell Biology

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Gingivitis, a common and mild form of gum disease can progress to periodontitis, a more serious infection that damages the soft tissue of the gums and sometimes even destroys the bone supporting the teeth. An international team of researchers and clinicians has charted the microbial ecology of the mouth at all stages of this progression, in nearly 1,000 women in Malawi. This work is laying a foundation of knowledge that could lead to better oral health. The research is published August 12 in Applied and Environmental Microbiology, a journal of the American Society for Microbiology.

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Cell division is a fundamental process of life, producing two cells from one single cell at each cell division. During animal development, a fertilized egg divides many times, increasing the number of cells, which are precisely organized within the animal's body. How many times a cell undergoes cell division and how the two daughter cells are positioned after the division can be critical for shaping the animal. Although the machinery essential for cell division is well characterized and evolutionarily conserved, it remains unknown in most animals how a cell division can become oriented relative to the animal's body axis. The work by Negishi et al., published recently in the electronic journal eLife, has revealed that in the sea squirt (Ciona intestinalis) embryo, the orientation of the cell division machinery in epithelial cells is controlled by a unique cell membrane structure, which we call an "invagination".

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Amateur and professional entomologists are experts at their own version of Pokémon Go. After all, part of their job is to search for and collect rare insect species that are stored in the archives of natural history museums.

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Whitehead Institute scientists have identified a potential antifungal mechanism that could enable combination therapy with fluconazole, one of today’s most commonly prescribed fungal infection treatments. Severe, invasive fungal infections have a mortality rate of 30-50% and cause an estimated 1.5 million deaths worldwide annually.

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Researchers at the Stowers Institute have identified a key molecule that directs stem cells in the planarian flatworm to make copies of themselves.

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Researchers at Mayo Clinic have reported a causal link between senescent cells — cells that accumulate with age and contribute to frailty and disease — and osteoarthritis in mice.

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Study maps out abnormal signaling pathways in prostate cancer cells and provides computational approaches to identify individualized targets for therapy

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Johns Hopkins researchers say they have identified a new disease gene that, when mutated, appears to increase the risk in a small number of people of developing emphysema and a lung-scarring condition known as pulmonary fibrosis.

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In a study spanning molecular genetics, stem cells and the sciences of both brain and behavior, researchers at University of California San Diego, with colleagues at the Salk Institute for Biological Studies and elsewhere, have created a neurodevelopmental model of a rare genetic disorder that may provide new insights into the underlying neurobiology of the human social brain.

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Many cancers only become a mortal danger if they form metastases elsewhere in the body. Such secondary tumours are formed when individual cells break away from the main tumour and travel through the bloodstream to distant areas of the body. To do so, they have to pass through the walls of small blood vessels. Scientists from the Max Planck Institute for Heart and Lung Research in Bad Nauheim and Goethe University Frankfurt have now shown that tumour cells kill specific cells in the vascular wall. This enables them to leave the vessels and establish metastases, a process facilitated by a molecule called DR6.

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A research team, led by Emeritus Professor Kazuhiro Nakaya of Japan's Hokkaido University, analyzed world-first footage captured by public broadcaster NHK in which two goblin sharks separately captured prey on a total of five occasions. The research has unraveled a century-old mystery surrounding how the deep-sea shark utilizes its protruding jaws, among other factors, to feed itself.

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University of Helsinki researchers have previously demonstrated that a point mutation in a gene of serotonin 2B receptor can render the carrier prone to impulsive behaviour, particularly when drunk. Now the research group has established that the same mutation may shield its bearers from obesity and insulin resistance, both of which are associated with type 2 diabetes.

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Michigan Technological University scientists have developed a process that could lead to stickier—and better—gene therapy drugs. The drugs, called antisense DNA, are made from short, single strands of synthetic DNA.

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Most molecular biologists look at how to switch on and regulate single genes. Scientists at the MRC Clinical Sciences Centre (CSC) have gone further, and have explored how to reawaken an entire set of inactive genes, a chromosome, that is present in every female human cell.

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Schizophrenic psychoses are a frequently occurring group of psychiatric disorders caused by a combination of biological, social and environmental factors. These disorders are associated with changes to the brain structure: for example, the hippocampus in the temporal lobe is usually smaller in affected individuals than in healthy ones. It is not yet known whether these changes to the brain structure are a result of the disorders and their accompanying medications, or whether they are already present before the onset of symptoms.

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A new study in mice suggests that in a tumor’s pre-clinical stages, long before a human tumor would be clinically recognizable, certain immune cells can recognize changes that make these cells behave as cancerous cells and attempt to launch an immune attack. However, the T cells that are recognizing these “driver” mutations in the tumor are rapidly turned off and then permanently silenced, making the cells non-functional and thereby protecting the tumor from an immune attack. If researchers can find a way to reverse that silencing, the tumor-recognizing T cells could be rescued and could potentially improve the performance of certain immunotherapies, including that of so-called checkpoint inhibitor drugs that release some of cancer’s brakes on the immune system.

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Cardiovascular diseases are the leading cause of death in the U.S. With one in every four deaths occurring each year, the five-year survival rate after a heart attack is worse than most cancers. A big part of the problem is the inability of the human heart to effectively repair itself after injury. A team of University of Houston researchers is trying to change that.

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About 7 percent of all Danish children are born prematurely. This is of significant im-portance not only to the child's development, but it also affects the mother's body that - unexpectedly - has to produce the necessary nutrition for the newborn baby.

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Maintaining proper levels of an essential helper molecule is crucial for optimal muscle function. Some athletes are already taking supplements to increase synthesis of this compound, called NAD, with the hopes of reversing the natural decay associated with aging of the mitochondria, the cell’s powerhouses. However, this is the first study to directly investigate the consequences of NAD deficiency on muscle function.

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Patients with sickle cell anemia (SCA) develop heart complications and nearly a quarter die a sudden death. Now, researchers have linked malfunctioning molecular pathways to specific heart anomalies in SCA that result from progressive fibrosis and result in sudden death. A study published online this week by PNAS (Proceedings of the National Academy of Sciences) reports the findings open a path to earlier non-invasive diagnosis and development of new targeted therapies to help SCA patients live longer with better quality of life.