The interaction between 20-hydroxyecdysone and AMPK through PI3K activation in Chinese mitten crab, Eriocheir sinensis

Dev Comp Immunol. 2024 Aug:157:105194. doi: 10.1016/j.dci.2024.105194. Epub 2024 May 14.

Abstract

In crustaceans, the steroid hormone 20-hydroxyecdysone (20E) initiates molting, and the molting process is also regulated by energy metabolism. AMPK is an energy sensor and plays a critical role in systemic energy balance. Here, the regulatory mechanism in the interaction between 20E and AMPK was investigated in Chinese mitten crab, Eriocheir sinensis. The results showed that the 20E concentration and the mRNA expression levels of 20E receptors in hepatopancreas were down-regulated post AMPK activator (AICAR) treatment, and were up-regulated after AMPK inhibitor (Compound C) injection in crabs. Besides, the molt-inhibiting hormone (MIH) gene expression in eyestalk showed the opposite patterns in response to the AICAR and Compound C treatment, respectively. Further investigation found that there was a significant reduction in 20E concentration post PI3K inhibitor (LY294002) treatment, and the phosphorylation level of PI3K was increased in hepatopancreas after AMPK inhibitor injection. On the other hand, the positive regulation of PI3K-mediated activation of AMPK was also observed, the phosphorylation levels of AMPKα, AMPKβ and PI3K in hepatopancreas were significantly increased post 20E injection. In addition, the phosphorylation levels of AMPKα and AMPKβ induced by 20E were decreased after the injection of PI3K inhibitor. Taken together, these results suggest that the regulatory cross-talk between 20E and AMPK is likely to act through PI3K pathway in E. sinensis, which appeared to be helpful for a better understanding in molting regulation.

Keywords: 20-hydroxyecdysone; AMPK; Eriocheir sinensis; PI3K.

MeSH terms

  • AMP-Activated Protein Kinases* / metabolism
  • Aminoimidazole Carboxamide / analogs & derivatives
  • Aminoimidazole Carboxamide / pharmacology
  • Animals
  • Arthropod Proteins / genetics
  • Arthropod Proteins / metabolism
  • Brachyura* / immunology
  • Chromones / pharmacology
  • Ecdysterone* / metabolism
  • Energy Metabolism
  • Hepatopancreas* / metabolism
  • Invertebrate Hormones / metabolism
  • Molting*
  • Morpholines / pharmacology
  • Phosphatidylinositol 3-Kinases* / metabolism
  • Phosphorylation
  • Ribonucleotides / pharmacology
  • Signal Transduction

Substances

  • Ecdysterone
  • AMP-Activated Protein Kinases
  • Phosphatidylinositol 3-Kinases
  • molt-inhibiting hormone
  • Invertebrate Hormones
  • Chromones
  • Aminoimidazole Carboxamide
  • AICA ribonucleotide
  • Ribonucleotides
  • Morpholines
  • Arthropod Proteins
  • 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one