Identification of natural products with neuronal and metabolic benefits through autophagy induction

Yuying Fan, Nan Wang, Altea Rocchi, Weiran Zhang, Robert Vassar, Yifa Zhou, Congcong He*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

68 Scopus citations

Abstract

Autophagy is a housekeeping lysosomal degradation pathway important for cellular survival, homeostasis and function. Various disease models have shown that upregulation of autophagy may be beneficial to combat disease pathogenesis. However, despite several recently reported small-molecule screens for synthetic autophagy inducers, natural chemicals of diverse structures and functions have not been included in the synthetic libraries, and characterization of their roles in autophagy has been lacking. To discover novel autophagy-regulating compounds and study their therapeutic mechanisms, we used analytic chemistry approaches to isolate natural phytochemicals from a reservoir of medicinal plants used in traditional remedies. From this pilot plant metabolite library, we identified several novel autophagy-inducing phytochemicals, including Rg2. Rg2 is a steroid glycoside chemical that activates autophagy in an AMPK-ULK1-dependent and MTOR-independent manner. Induction of autophagy by Rg2 enhances the clearance of protein aggregates in a cell-based model, improves cognitive behaviors in a mouse model of Alzheimer disease, and prevents high-fat diet-induced insulin resistance. Thus, we discovered a series of autophagy-inducing phytochemicals from medicinal plants, and found that one of the compounds Rg2 mediates metabolic and neurotrophic effects dependent on activation of the autophagy pathway. These findings may help explain how medicinal plants exert the therapeutic functions against metabolic diseases.

Original languageEnglish (US)
Pages (from-to)41-56
Number of pages16
JournalAutophagy
Volume13
Issue number1
DOIs
StatePublished - Jan 2 2017

Funding

We thank the Northwestern University Behavioral Phenotyping Core, Mouse Histology and Phenotyping Laboratory and Center for Advanced Microscopy for technical support and assistance, Beth Levine (University of Texas Southwestern Medical Center) for providing BCL2AAA mice and prkaa1 prkaa2 null MEFs, Noboru Mizushima (University of Tokyo) for providing GFP-LC3 transgenic mice, Ai Yamamoto (Columbia University) for providing HeLa cells stably expressing CFP-HTT25Q, CFP-HTT65Q and CFP-HTT103Q, and suggestions on the manuscript, and Katherine Sadleir (Northwestern University) for advice and protocols on 5XFAD mice, Aβ42 dot blots and cerebral amyloid imaging. Y. Z. was supported by the grant from National Natural Science Foundation of China (No. 31470798) and the Doctoral Fund of Ministry of Education of China (No. 20120043130001). R. V. was supported by grants from National Institutes of Health (AG022560 and AG030142). Y. F., A. R., N. W., W. Z. and C. H. were supported by the startup funds from Northwestern University and the grant from National Institutes of Health (DK094980). Y. F. was also supported by the Chinese Scholarship Council (CSC) and National Natural Science Foundation of China (Grant No. 31300287). N. W. was also supported by the National Natural Science Foundation of China (Grant No. 31171303).

Keywords

  • AMPK
  • Alzheimer's disease
  • amyloid
  • autophagy induction
  • ginsenoside
  • glycoconjugate
  • insulin resistance
  • medicinal plant
  • phytochemical

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

Fingerprint

Dive into the research topics of 'Identification of natural products with neuronal and metabolic benefits through autophagy induction'. Together they form a unique fingerprint.

Cite this