温暖化世界で人類の寿​​命を延ばす可能性があるタンパク質

新しい研究は、温暖な気候での寿命は代謝率の増加によって受動的に短くなるだけでなく、コラーゲンの発現を制御するNPR-8と呼ばれる神経系タンパク質によって積極的に調節されることを示しています。 研究者らは、このタンパク質を欠く線虫は、気温が上昇するとコラーゲンの発現が増加し、その結果、ストレスに対する抵抗力が増し、加齢に伴う皮膚のしわが減り、寿命が延びることを発見し、その根底にあるメカニズムを利用して、地球温暖化が進む中で人間の寿命を延ばすことができる可能性を示唆した。気温です。 。

科学者たちは長い間、多くの生物は温暖な環境よりも涼しい環境の方が寿命が長い傾向があることに気づいてきました。 に関する最近の研究 線虫線虫の一種であるこの寿命は、さまざまな動物の皮膚、骨、結合組織の主成分であるコラーゲンの生成を調節する神経系の特定のタンパク質に関連している可能性があることを示唆しています。

タンパク質が含まれていることを考えると、 線虫 他の細胞で見られる神経系受容体タンパク質と非常によく似ています。[{” attribute=””>species, including humans, this revelation could potentially bring us a step closer to finding methods to manipulate collagen production in order to slow human aging and enhance lifespan, particularly in the context of rising global temperatures. The research, led by a team from Washington State University, was published in the journal Aging Cell.

“Based on animal studies, scientists anticipate that human lifespan will go down in the future as climate change drives up the ambient temperature,” said senior author Yiyong (Ben) Liu, an assistant professor in the WSU Elson S. Floyd College of Medicine and director of the university’s Genomics Service Center. “We have found that warm temperatures leading to short lifespan is not a passive, thermodynamic process as previously thought, but a regulated process controlled by the nervous system. Our findings mean that down the road, it may be possible to intervene in that process to extend human lifespan as temperatures rise.”

Scanning electron microscopy images of the cuticle (skin) of C. elegans kept at 25 degrees Celsius show wrinkles on an old (9-day old) adult wild-type worm (left) but smooth skin on an npr-8 mutant worm of the same age (right). Yiyong (Ben) Liu, Washington State University

The researchers looked at a nervous system protein known as NPR-8 in the tiny soil-dwelling worm Caenorhabditis elegans (C. elegans), a commonly used model organism in aging research. During their study, they observed that worms lacking NPR-8 had fewer skin wrinkles as they aged. They also made the unexpected discovery that mutant worms kept at a warm temperature of 25 C (77 F) had increased collagen expression and lived longer than wild-type worms, which did not happen when the worms were kept at 20 C or 15 C (68 F and 59 F, respectively). To determine whether the neural regulation of collagens may play a role in aging and longevity, they conducted a series of additional experiments and analyses.

“What we saw was that the absence of NPR-8 caused an increase in collagen expression, which increased the worms’ stress resistance and lifespan and made them look younger than wild-type worms that were the same biological age,” said co-first author Durai Sellegounder, a former postdoctoral research associate in the WSU Elson S. Floyd College of Medicine who is now a scientist at the Buck Institute for Research on Aging.

Study author Durai Sellegounder uses a microinjection microscope to create genetically modified C. elegans for an experiment. Credit: Cori Kogan, Washington State University

In one experiment, the researchers reintroduced NPR-8 in mutant worms kept at 25 C and saw that this reverted the worms’ skin from smooth to wrinkled and significantly reduced the animals’ extended lifespan. Next, they showed that the extended lifespan of npr-8 mutant worms also held up under heat stress conditions, with mutant worms surviving significantly longer than wild-type worms when moved into a 35 C (95 F) environment. Additional experiments identified specific neurons responsible for regulating lifespan in response to warm temperatures and pointed to increased expression of collagens as a driver of the improved lifespan at warm temperatures.

The phenomenon of heat shortening lifespan has traditionally been explained by the rate of living theory, which suggests that heat speeds up an organism’s metabolism, causing it to use up its finite store of metabolic energy more quickly. While the researchers still found limited evidence supporting this idea, their study findings indicate that the nervous system also plays an active role in this process.

Given earlier findings that showed that worms lacking NPR-8 were more resistant to infection and oxidative stress, the researchers believe that the NPR-8-controlled increase in collagen expression boosts the animals’ resistance to stressful conditions such as excessive heat. Their next step is to delve deeper into the underlying mechanisms of how increased collagen production enhances stress resistance.

Reference: “The longevity response to warm temperature is neurally controlled via the regulation of collagen genes” by Sankara Naynar Palani, Durai Sellegounder, Phillip Wibisono and Yiyong Liu, 9 March 2023, Aging Cell.
DOI: 10.1111/acel.13815

In addition to Liu and Sellegounder, co-authors on the current study include co-first author and postdoctoral research associate Sankara Naynar Palani and postdoctoral research associate Phillip Wibisono, both of the WSU Elson S. Floyd College of Medicine.