文献类型： 外文期刊

作者： Wang, Yong ¹ ; Buer, Benjamin ² ; Goodman, Cynthia L. ³ ; Kang, David ³ ; Reall, Tamra ⁴ ; Dohn, Susanne ² ; Ringbauer, Joseph ³ ; Li, Yaofa ⁵ ; Geibel, Sven ² ; Stanley, David ³ ;

作者机构： 1.Shenyang Agr Univ, Coll Biosci & Biotechnol, Liaoning Engn & Technol Res Ctr Insect Resource, Shenyang, Peoples R China

2.Bayer AG, Res & Dev, Crop Sci, Monheim Am Rhein, Germany

3.USDA ARS, Biol Control Insects Res Lab, Columbia, MO USA

4.Univ Missouri Extens, Blue Springs, MO USA

5.Hebei Acad Agr & Forestry Sci, Plant Protect Inst, IPM Ctr Hebei Prov, Key Lab Integrated Pest Management Crops Northern, Baoding, Peoples R China

6.USDA ARS, Biol Control Insects Res Lab, 1503 South Providence Rd, Columbia, MO 65203 USA

关键词： 20-hydroxyecdysone; indomethacin; insect cell line; insect nervous system; lepidoptera; prostaglandin; Spodoptera frugiperda

期刊名称：ARCHIVES OF INSECT BIOCHEMISTRY AND PHYSIOLOGY （ 影响因子：2.2； 五年影响因子：2.1 ）

ISSN： 0739-4462

年卷期： 2024 年 115 卷 2 期

页码：

收录情况： SCI

摘要： Insecticide mode of action studies provide insights into how new insecticidal actives function and contribute to assessing safety to humans and nontarget organisms. Insect cell lines that express potential target sites can serve as valuable tools in this effort. In this paper, we report on the influence of two signaling molecules on protein expression in a nervous system cell line established from Spodoptera frugiperda (Bayer/BCIRL-SfNS2-0714-TR). We selected this line because we established it in our laboratory and we are experienced in using it. Cells were exposed to the insect developmental hormone (1 mu g/mL 20-hydroxyecdysone, 20E) and/or a cyclooxygenase (COX) inhibitor (25 mu M indomethacin, INDO; inhibits prostaglandin [PG] biosynthesis) for 24 h (Day 2), 72 h (Day 4), or 120 h (Day 6). We selected a PG biosynthesis inhibitor because PGs act in many aspects of insect biology, such as embryonic development, immunity, and protein phosphorylation. We selected the developmental hormone, 20E, because it also acts in fundamental aspects of insect biology. We identified specific proteins via in silico analysis. Changes in protein expression levels were determined using liquid chromatography-mass spectrometry (MS) + MS-MS. The largest number of changes in protein expression occurred on Day 2. The combination of 20E plus INDO led to 222 differentially expressed proteins, which documents the deep significance of PGs and 20E in insect biology. 20E and, separately, INDO led to changes in 30 proteins each (p value < 0.01; >2X or <0.5X-fold changes). We recorded changes in the expression of 9 or 12 proteins (20E), 10 or 6 proteins (INDO), and 21 or 20 proteins (20E + INDO) on D4 and D6, respectively. While the cell line was established from neuronal tissue, the differentially expressed proteins act in a variety of fundamental cell processes. In this paper, we moved beyond a list of proteins by providing detailed, Gene Ontology term analyses and enrichment, which offers an in-depth understanding of the influence of these treatments on the SfNS2 cells. Because proteins are active components of cell physiology in their roles as enzymes, receptors, elements of signaling transduction pathways, and cellular structures, changes in their expression levels under the influence of signaling molecules provide insights into their function in insect cell physiology.