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Would you like to live forever? Some billionaires, already invincible in every other way, have decided that they also deserve not to die. Today several biotech companies, fueled by Silicon Valley fortunes, are devoted to “life extension” — or as some put it, to solving “the problem of death.”


Some very wealthy people are serious about outsmarting mortality.

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Summary: Google’s ultra-secretive Calico Labs announces a significant discovery – the naked mole rat is the first and only non-aging mammal and shows little signs of aging as it gets older. [This article first appeared on the website LongevityFacts.com. Author: Brady Hartman. ]

With wrinkly skin and completely bald, the naked mole rat is one of the ugliest creatures around but lives an exceptionally long life for a small mammal. It rarely develops the chronic diseases of aging such as cancer and lives 10 times longer than regular rats.

The First Non-Aging Mammal

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A team of researchers with the Ulsan National Institute of Science and Technology in the Republic of Korea has developed a glucose monitoring contact lens that its makers claim is comfortable enough to wear. In their paper published on the open access site Science Advances, the group describes their contact lens and suggests it could be ready for commercial use within five years.

Diabetes results in unmanageable , requiring those who have the disease to monitor and adjust them with insulin or medicine. Monitoring, unfortunately, requires pricking a finger to retrieve a blood sample for testing, which most people do not like. For that reason, scientists seek another way. A new method employs a . Prior research has shown glucose levels in tears follows that of glucose levels in the blood in many respects. To date, there are no commercially available contact products because, as the researchers note, they are made of hard materials that are uncomfortable in the eye. They claim to have overcome that problem by breaking apart the pieces of their sensing device and encapsulating each in a soft polymer and then connecting them together in a flexible mesh.

The polymer is the same type used in conventional contact lenses. The components of the device consist of a graphene-based sensor, a rectifier, LED display and a stretchable antenna. Power for the sensor is still external—it is held in the air a minimum of nine millimeters from the lens. The LED glows during normal conditions and turns off when high levels of are detected. The flexibility of the lens and sensor components also allows for removal of the device in the same way as normal contact lenses—by grabbing and bending.

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In a new study, researchers propose that TIGIT is a marker of T cell senescence and exhaustion in the immune system. However, not only is TIGIT just a biomarker, it is also a potential therapeutic target; as the researcher team discovered, lowering levels of TIGIT resulted in the restoration of some lost function in T cell populations that were experiencing high levels of senescence and exhaustion.


In a new study, researchers propose that TIGIT is a marker of T cell senescence and exhaustion in the immune system[1]. However, not only is TIGIT just a biomarker, it is also a potential therapeutic target; as the researcher team discovered, lowering levels of TIGIT resulted in the restoration of some lost function in T cell populations that were experiencing high levels of senescence and exhaustion.

Aging is associated with immune dysfunction, especially T-cell defects, which result in increased susceptibility to various diseases. Previous studies showed that T cells from aged mice express multiple inhibitory receptors, providing evidence of the relationship between T-cell exhaustion and T-cell senescence. In this study, we showed that T-cell immunoglobulin and immunoreceptor tyrosine-based inhibitory motif (ITIM) domain (TIGIT), a novel co-inhibitory receptor, was upregulated in CD8 + T cells of elderly adults. Aged TIGIT + CD8 + T cells expressed high levels of other inhibitory receptors including PD-1 and exhibited features of exhaustion such as downregulation of the key costimulatory receptor CD28, representative intrinsic transcriptional regulation, low production of cytokines, and high susceptibility to apoptosis. Importantly, their functional defects associated with aging were reversed by TIGIT knockdown.

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Since the birth of Dolly the sheep in 1996, scientists across the globe have used the same technique to clone nearly two dozen other animal species, including cats, dogs, rats, and cattle. Primates, however, had proven resistant to the process — until now.

In a new study published in Cell, a team of Chinese researchers led by Qiang Sun at the Chinese Academy of Sciences Institute of Neuroscience in Shanghai reveal that they’ve found a way to tweak the Dolly cloning technique to make it work in primates. Their efforts have resulted in the birth of two cloned female macaques: Zhong Zhong and Hua Hua.

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