PGE<sub>2</sub> Binding Affinity of Hemocyte Membrane Preparations of <i>Manduca sexta</i> and Identification of the Receptor‐Associated G Proteins in Two Lepidopteran Species

Prostaglandin E<sub>2</sub> (PGE<sub>2</sub>) is an eicosanoid that mediates a range of physiological actions in vertebrates and invertebrates, including reproduction and immunity. The PGE<sub>2</sub> receptor was identified and functionally assessed in two lepidopteran insects, Manduca sexta and Spodoptera exigua. However, its binding affinity to the receptor has not been reported. The PGE<sub>2</sub> receptor is a G-protein coupled receptor (GPCR) although its corresponding G-protein is not identified. PGE<sub>2</sub> binding assays were performed with membrane preparations from hemocytes of M. sexta larvae. We recorded an optimal binding in 4 h reactions conducted at pH 7.5 with 12 nM tritium-labeled PGE<sub>2</sub>. We found that hemocytes express a single population of PGE<sub>2</sub> binding sites with a high affinity (Kd = 35 pmol/mg protein), which are specific and saturable. The outcomes of experiments on the influence of purine nucleotides suggested these are functional GPCRs. A bioinformatics analysis led to a proposed trimeric G-protein in the S. exigua transcriptome, in which the Gα subunit is classified into five different types: Gα(o), Gα(q), Gα(s), Gα(12), and Gα(f). After confirming expressions of these five types in S. exigua, individual RNA interference (RNAi) treatments were applied to the larvae using gene-specific double-stranded RNAs. RNAi treatments specific to Gα(s) or Gα(12) gene expression significantly suppressed the cellular immune responses although the RNAi treatments specific to other three Gα components did not. While PGE<sub>2</sub> treatments led to elevated hemocyte cAMP or Ca<sup>2+</sup> levels, the RNAi treatments specific to Gα(s) or Gα(12) genes led to significantly reduced second messenger levels under PGE<sub>2,</sub> although the RNAi treatments specific to the other three Gα components did not. These results showed that the PGE<sub>2</sub> receptor has high PGE<sub>2</sub> affinity in the nanomolar range and binds G-proteins containing a Gα(s) or Gα(12) trimeric component in S. exigua and M. sexta, and likely, all lepidopteran insects.

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Publication Details

Journal
Archives of Insect Biochemistry and Physiology
Published
2024-11-01
DOI
https://doi.org/10.1002/arch.70005
Citations
3
Primary Topic
Invertebrate Immune Response Mechanisms
Type
article
Field-Weighted Citation Impact
0.72

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article

PGE2 Binding Affinity of Hemocyte Membrane Preparations of Manduca sexta and Identification of the Receptor‐Associated G Proteins in Two Lepidopteran Species

Falguni Khan, Hasan Tunaz, Eric J. Haas, Yonggyun Kim et al.
3 citations
Archives of Insect Biochemistry and Physiology
Invertebrate Immune Response Mechanisms
0.72
article

PGE2 Binding Affinity of Hemocyte Membrane Preparations of Manduca sexta and Identification of the Receptor‐Associated G Proteins in Two Lepidopteran Species

Falguni Khan, Hasan Tunaz, Eric J. Haas, Yonggyun Kim, DAVID W. STANLEY
article en
3 citations

Abstract

Prostaglandin E<sub>2</sub> (PGE<sub>2</sub>) is an eicosanoid that mediates a range of physiological actions in vertebrates and invertebrates, including reproduction and immunity. The PGE<sub>2</sub> receptor was identified and functionally assessed in two lepidopteran insects, Manduca sexta and Spodoptera exigua. However, its binding affinity to the receptor has not been reported. The PGE<sub>2</sub> receptor is a G-protein coupled receptor (GPCR) although its corresponding G-protein is not identified. PGE<sub>2</sub> binding assays were performed with membrane preparations from hemocytes of M. sexta larvae. We recorded an optimal binding in 4 h reactions conducted at pH 7.5 with 12 nM tritium-labeled PGE<sub>2</sub>. We found that hemocytes express a single population of PGE<sub>2</sub> binding sites with a high affinity (Kd = 35 pmol/mg protein), which are specific and saturable. The outcomes of experiments on the influence of purine nucleotides suggested these are functional GPCRs. A bioinformatics analysis led to a proposed trimeric G-protein in the S. exigua transcriptome, in which the Gα subunit is classified into five different types: Gα(o), Gα(q), Gα(s), Gα(12), and Gα(f). After confirming expressions of these five types in S. exigua, individual RNA interference (RNAi) treatments were applied to the larvae using gene-specific double-stranded RNAs. RNAi treatments specific to Gα(s) or Gα(12) gene expression significantly suppressed the cellular immune responses although the RNAi treatments specific to other three Gα components did not. While PGE<sub>2</sub> treatments led to elevated hemocyte cAMP or Ca<sup>2+</sup> levels, the RNAi treatments specific to Gα(s) or Gα(12) genes led to significantly reduced second messenger levels under PGE<sub>2,</sub> although the RNAi treatments specific to the other three Gα components did not. These results showed that the PGE<sub>2</sub> receptor has high PGE<sub>2</sub> affinity in the nanomolar range and binds G-proteins containing a Gα(s) or Gα(12) trimeric component in S. exigua and M. sexta, and likely, all lepidopteran insects.

Archives of Insect Biochemistry and PhysiologyVol. 117(3)
Gyeongguk National University (KR), Creighton University (US), Biological Control of Insects Research Laboratory (US), Kahramanmaraş Sütçü İmam University (TR)
U.S. Department of Agriculture
Openalex Percentile: Top 28%
Invertebrate Immune Response Mechanisms
0.72
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