Mingjun Wang , Wenhui Guo , Yong Yang , Qingyao Zhu , Xiaohong Zhang , Daochuan Zhang
{"title":"LmSPARC基因敲低影响迁徙蝗卵巢发育过程中的脂质代谢稳态。","authors":"Mingjun Wang , Wenhui Guo , Yong Yang , Qingyao Zhu , Xiaohong Zhang , Daochuan Zhang","doi":"10.1016/j.jinsphys.2025.104855","DOIUrl":null,"url":null,"abstract":"<div><div>Reproduction, a fundamental feature of all known life, is closely correlated with energy homeostasis. Lipids, which can accumulate, provide essential energy support for reproduction. Secreted Protein, Acidic and Rich in Cysteine (SPARC) is a cellular matrix glycoprotein involved in the regulation of extracellular matrix synthesis. However, the precise coordination of lipid homeostasis by SPARC during insect reproductive development remains poorly understood. Our study revealed that when the expression of <em>LmSPARC</em> was downregulated by RNA interference (RNAi) in 4th and 5th instar nymphs, molting was delayed compared with that in the control. Knockdown of <em>LmSPARC</em> reduced levels of vitellogenin (Vg) protein and retarded maturation of oocytes. The intercellular patency in the follicular epithelium of the ovaries was abnormal after <em>LmSPARC</em> silencing. In addition, transcriptomic and metabolomic analyses showed that the energy metabolism pathway was disrupted in locusts lacking <em>LmSPARC</em>, and the accumulation and degradation of lipids in the body were abnormal. This study provides insights into the effects of <em>LmSPARC</em> on ovarian development and energy metabolism homeostasis in <em>Locusta migratoria</em>, and provides a reference for screening biological control targets via on RNAi.</div></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"165 ","pages":"Article 104855"},"PeriodicalIF":2.3000,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Knockdown of LmSPARC influences lipid metabolic homeostasis involved ovarian development in Locusta migratoria\",\"authors\":\"Mingjun Wang , Wenhui Guo , Yong Yang , Qingyao Zhu , Xiaohong Zhang , Daochuan Zhang\",\"doi\":\"10.1016/j.jinsphys.2025.104855\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Reproduction, a fundamental feature of all known life, is closely correlated with energy homeostasis. Lipids, which can accumulate, provide essential energy support for reproduction. Secreted Protein, Acidic and Rich in Cysteine (SPARC) is a cellular matrix glycoprotein involved in the regulation of extracellular matrix synthesis. However, the precise coordination of lipid homeostasis by SPARC during insect reproductive development remains poorly understood. Our study revealed that when the expression of <em>LmSPARC</em> was downregulated by RNA interference (RNAi) in 4th and 5th instar nymphs, molting was delayed compared with that in the control. Knockdown of <em>LmSPARC</em> reduced levels of vitellogenin (Vg) protein and retarded maturation of oocytes. The intercellular patency in the follicular epithelium of the ovaries was abnormal after <em>LmSPARC</em> silencing. In addition, transcriptomic and metabolomic analyses showed that the energy metabolism pathway was disrupted in locusts lacking <em>LmSPARC</em>, and the accumulation and degradation of lipids in the body were abnormal. This study provides insights into the effects of <em>LmSPARC</em> on ovarian development and energy metabolism homeostasis in <em>Locusta migratoria</em>, and provides a reference for screening biological control targets via on RNAi.</div></div>\",\"PeriodicalId\":16189,\"journal\":{\"name\":\"Journal of insect physiology\",\"volume\":\"165 \",\"pages\":\"Article 104855\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-07-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of insect physiology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S002219102500109X\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENTOMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of insect physiology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S002219102500109X","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
Knockdown of LmSPARC influences lipid metabolic homeostasis involved ovarian development in Locusta migratoria
Reproduction, a fundamental feature of all known life, is closely correlated with energy homeostasis. Lipids, which can accumulate, provide essential energy support for reproduction. Secreted Protein, Acidic and Rich in Cysteine (SPARC) is a cellular matrix glycoprotein involved in the regulation of extracellular matrix synthesis. However, the precise coordination of lipid homeostasis by SPARC during insect reproductive development remains poorly understood. Our study revealed that when the expression of LmSPARC was downregulated by RNA interference (RNAi) in 4th and 5th instar nymphs, molting was delayed compared with that in the control. Knockdown of LmSPARC reduced levels of vitellogenin (Vg) protein and retarded maturation of oocytes. The intercellular patency in the follicular epithelium of the ovaries was abnormal after LmSPARC silencing. In addition, transcriptomic and metabolomic analyses showed that the energy metabolism pathway was disrupted in locusts lacking LmSPARC, and the accumulation and degradation of lipids in the body were abnormal. This study provides insights into the effects of LmSPARC on ovarian development and energy metabolism homeostasis in Locusta migratoria, and provides a reference for screening biological control targets via on RNAi.
期刊介绍:
All aspects of insect physiology are published in this journal which will also accept papers on the physiology of other arthropods, if the referees consider the work to be of general interest. The coverage includes endocrinology (in relation to moulting, reproduction and metabolism), pheromones, neurobiology (cellular, integrative and developmental), physiological pharmacology, nutrition (food selection, digestion and absorption), homeostasis, excretion, reproduction and behaviour. Papers covering functional genomics and molecular approaches to physiological problems will also be included. Communications on structure and applied entomology can be published if the subject matter has an explicit bearing on the physiology of arthropods. Review articles and novel method papers are also welcomed.