β-Arrestin1 interacts with G protein-coupled receptor to desensitize signaling of the steroid hormone 20-hydroxyecdysone in the lepidopteran insect Helicoverpa armigera
Abstract
The steroid hormone 20-hydroxyecdysone (20E) plays a critical role in insect development, particularly in larval molting and larval-pupal transition. Studies have indicated that 20E transmits its signal via a G protein-coupled receptor (GPCR)-mediated non-genomic pathway before a genomic pathway is initiated. However, the mechanism by which a 20E signal is desensitized remains unclear. We proposed that β-arrestin1 interacts with ecdysone-responsible GPCR (ErGPCR1) to desensitize a 20E signal in the lepidopteran insect Helicoverpa armigera. Results showed that β-arrestin1 was highly expressed in various tissues during metamorphosis. β-Arrestin1 knockdown by RNA interference in larvae caused advanced pupation and a larval-pupal chimera. The mRNA levels of 20E-response genes were increased after β-arrestin1 was knocked down but were decreased after β-arrestin1 was overexpressed. 20E induced the migration of β-arrestin1 from the cytosol to the cytoplasmic membrane to interact with ErGPCR1. The inhibitors suramin and chelerythrine chloride repressed 20E-induced β-arrestin1 phosphorylation and membrane migration. With ErGPCR1, 20E regulated β-arrestin1 phosphorylation on serines at positions 170 and 234. The double mutation of the amino acids Ser170 and Ser234 to asparagine inhibited phosphorylation and membrane migration of β-arrestin1 in 20E induction. Therefore, 20E via ErGPCR1 and PKC signaling induces β-arrestin1 phosphorylation; phosphorylated β-arrestin1 migrates to the cytoplasmic membrane to interact with ErGPCR1 to block 20E signaling via a feedback mechanism.
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β-arrestin-1 expression levels are markedly increased in tissues during H. armigera metamorphosis.
“A study in H. armigera showed that β-arrestin-1 expression levels are markedly increased in tissues during H. armigera metamorphosis [62].”
From G protein-coupled receptors function as cell membrane receptors for the steroid hormone 20-hydroxyecdysone (2020) · cites this paper as [62]
Via a negative feedback mechanism, 20E induces β-arrestin-1 phosphorylation and cell membrane migration, which blocks 20E signaling by the interaction between β-arrestin-1 and ErGPCR-1.
“Therefore, via negative feedback mechanism, 20E induces β-arrestin-1 phosphorylation and cell membrane migration, which blocks 20E signaling by the interaction between β-arrestin-1 and ErGPCR-1 [62].”
From G protein-coupled receptors function as cell membrane receptors for the steroid hormone 20-hydroxyecdysone (2020) · cites this paper as [62]
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- Authors
- Zhang, X.-Q., Li, X.-R., Ren, J., Li, Y.-B., Cai, M.-J., Wang, J.-X., & Zhao, X.-F.
- Affiliations
- Shandong University (CN)
- Corresponding author
- Zhao, Xiao-Fan
- Venue
- Cellular Signalling
- Publisher
- Elsevier BV
- Published
- 2015-04
- Volume
- 27
- Issue
- 4
- Pages
- 878-886
- ISSN
- 0898-6568 (ISSN-L)
- OpenAlex
- W1970460358
- Cited by
- 7
- References
- 48
- Citations by year
- 2026: 1 · 2024: 1 · 2021: 3 · 2020: 1 · 2016: 1
- FWCI
- 0.14
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cellular Signalling (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Key Research and Development Program of China (2012CB114101)
- National Natural Science Foundation of China (31230067)
- Ministry of Education of the People's Republic of China (20120131110025)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Keywords
- β-arrestin1, 20-hydroxyecdysone, Helicoverpa armigera, receptor desensitization, steroid hormone signaling, protein kinase C, feedback signaling, larval-pupal transition, metamorphosis, membrane translocation
- MeSH terms
- beta-Arrestins, Animals, Cell Line, Ecdysterone, Lepidoptera, Metamorphosis, Biological, Molecular Sequence Data, Phosphorylation, Protein Kinase C, Signal Transduction, Arrestins, Insect Proteins, Receptors, G-Protein-Coupled, Gene Knockdown Techniques
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