Shuhei Nakamura, Tamotsu Yoshimori ≪Genetics≫ The key to increased lifespan? Rubicon alters autophagy in animals during aging
2019-02-19 Publish Nature Communications Osaka University-led study shows that increased expression of Rubicon in tissues from aged animals contributed to reduced levels of autophagy, which may lead to aging progression Autophagy is an important biological recycling mechanism that is used to maintain homeostasis (balance or equilibrium) within all types of animal tissue. Many studies have attempted to understand the relationship between the reduction of autophagy and progression of aging in animals; however, none have provided a clear explanation, until now. In 2009, a research team led by Tamotsu Yoshimori at Osaka University identified Rubicon as a protein factor that suppresses autophagy by controlling a specific step in this pathway. This time, the team found that Rubicon expression levels increased in an age-related manner in worm, fly, and mouse tissues, publishing their findings in Nature Communications. Autophagy allows degradation of damaged cellular components and helps to avoid the onset of a variety of diseases related to cellular stress and dysfunction, including cancer, neurodegenerative diseases, and metabolic syndromes. Reduced autophagy has recently been linked to progression of aging in animals. While a variety of methods can increase autophagy in aged animals, thereby slowing the aging process, there has been no definite finding regarding the underlying cause of naturally reduced autophagy. “Rubicon has been linked to inhibition of the autophagic process, and knockout of Rubicon in mice helped to mitigate autophagy-related liver diseases,” says Yoshimori. “Therefore, we suspected that Rubicon may directly affect aging through its interaction with autophagy.” In the study, increased levels of Rubicon were found in tissues from multiple aged model organisms (worms, flies, and mice). When the researchers suppressed Rubicon expression, all model organisms demonstrated increased autophagy activity, which led to improvement of multiple age-related factors and slightly increased lifespan in worms and flies. “Our analyses revealed that Rubicon suppression in model organisms led to reduction of age-associated motor decline, as well as reduction of fibrosis,” says Shuhei Nakamura, lead author on the study. “Importantly, we found that Rubicon suppression enabled aged mice to resist attempts to induce Parkinson’s disease.” The findings in this study suggest that, because elevated levels of Rubicon lead to reduced autophagy in aged animals, suppression of Rubicon may be critical in extending healthy lifespan in humans. *** *** Funding: Japan Society for the Promotion of Science (JSPS); Japan Agency for Medical Research and Development (AMED) Summary: Primary keyword: Medicine/Health
The article, “Suppression of autophagic activity by Rubicon is a signature of aging,” was published in Nature Communications at DOI: https://doi.org/10.1038/s41467-019-08729-6.
Article: Suppression of autophagic activity by Rubicon is a signature of aging
Journal: Nature Communications
DOI: 10.1038/s41467-019-08729-6
Authors: Shuhei Nakamura, Masaki Oba, Mari Suzuki, Atsushi Takahashi, Tadashi Yamamuro, Mari Fujiwara, Kensuke Ikenaka, Satoshi Minami, Namine Tabata, Kenichi Yamamoto, Sayaka Kubo, Ayaka Tokumura, Kanako Akamatsu, Yumi Miyazaki, Tsuyoshi Kawabata, Maho Hamasaki, Koji Fukui, Kazunori Sango, Yoshihisa Watanabe, Yoshitsugu Takabatake, Tomoya S. Kitajima, Yukinori Okada, Hideki Mochizuki, Yoshitaka Isaka, Adam Antebi and Tamotsu Yoshimori
Autophagy is an important biological recycling mechanism that influences the progression of aging in animals. Here, age-related changes in autophagy were studied in multiple model organisms. An Osaka University-led research team found that Rubicon suppression led to reduction of age-associated motor decline, as well as reduction of fibrosis, and that Rubicon could be an important new target for treatments designed to reduce the effects of aging in humans.
Additional keywords: Cell Biology, Mortality/Longevity, Aging, Neurobiology, Parkinson’s Disease, Metabolism/Metabolic Diseases
Categories: Medical, Life Sciences
