Xianliang Huang , Yuxing Xiao , Yaru Yang , Jiaqi Duan , Deguang Liu
{"title":"血青素有助于迁徙蝗虫对缺氧的胚胎适应。","authors":"Xianliang Huang , Yuxing Xiao , Yaru Yang , Jiaqi Duan , Deguang Liu","doi":"10.1016/j.jinsphys.2025.104750","DOIUrl":null,"url":null,"abstract":"<div><div>Ambient hypoxia can pose a major threat to the survival of metazoan organisms, especially insect embryos. Hemocyanin exhibits dominant expression in insect embryos, but its specific roles in hypoxia adaptation remain unexplored. Soil-dwelling locust eggs may frequently experience hypoxia during development. A comprehensive analysis of physiological and biochemical characters of hemocyanin was conducted in the embryos of migratory locust <em>Locusta migratoria</em>. Our results demonstrated that the revolution process was the critical hypoxia-sensitive event during locust embryogenesis. Hemocyanin presented a prominent expression in the revolution stage and exhibited strong responses to hypoxia. The relative duration of revolution was correlated negatively with the expression of hemocyanin subunit 2 (HC2), suggesting that HC2 might be closely associated with hypoxia adaptation of locust embryos. Furthermore, a <em>HC2</em> mutant locust strain was established using the CRISPR/Cas9 technology, and higher hypoxia sensitivity was found for HC2-deficient locust embryos. Knockdown of <em>HC2</em> increased anaerobic metabolism and oxidative stress while reducing oxidative metabolism. Overall, these findings clearly demonstrated the pivotal roles of hemocyanin in hypoxia adaptation of insect embryos.</div></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"161 ","pages":"Article 104750"},"PeriodicalIF":2.3000,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Hemocyanin contributes to embryonic adaptation to hypoxia in the migratory locust\",\"authors\":\"Xianliang Huang , Yuxing Xiao , Yaru Yang , Jiaqi Duan , Deguang Liu\",\"doi\":\"10.1016/j.jinsphys.2025.104750\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Ambient hypoxia can pose a major threat to the survival of metazoan organisms, especially insect embryos. Hemocyanin exhibits dominant expression in insect embryos, but its specific roles in hypoxia adaptation remain unexplored. Soil-dwelling locust eggs may frequently experience hypoxia during development. A comprehensive analysis of physiological and biochemical characters of hemocyanin was conducted in the embryos of migratory locust <em>Locusta migratoria</em>. Our results demonstrated that the revolution process was the critical hypoxia-sensitive event during locust embryogenesis. Hemocyanin presented a prominent expression in the revolution stage and exhibited strong responses to hypoxia. The relative duration of revolution was correlated negatively with the expression of hemocyanin subunit 2 (HC2), suggesting that HC2 might be closely associated with hypoxia adaptation of locust embryos. Furthermore, a <em>HC2</em> mutant locust strain was established using the CRISPR/Cas9 technology, and higher hypoxia sensitivity was found for HC2-deficient locust embryos. Knockdown of <em>HC2</em> increased anaerobic metabolism and oxidative stress while reducing oxidative metabolism. Overall, these findings clearly demonstrated the pivotal roles of hemocyanin in hypoxia adaptation of insect embryos.</div></div>\",\"PeriodicalId\":16189,\"journal\":{\"name\":\"Journal of insect physiology\",\"volume\":\"161 \",\"pages\":\"Article 104750\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-01-15\",\"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/S0022191025000046\",\"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/S0022191025000046","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
Hemocyanin contributes to embryonic adaptation to hypoxia in the migratory locust
Ambient hypoxia can pose a major threat to the survival of metazoan organisms, especially insect embryos. Hemocyanin exhibits dominant expression in insect embryos, but its specific roles in hypoxia adaptation remain unexplored. Soil-dwelling locust eggs may frequently experience hypoxia during development. A comprehensive analysis of physiological and biochemical characters of hemocyanin was conducted in the embryos of migratory locust Locusta migratoria. Our results demonstrated that the revolution process was the critical hypoxia-sensitive event during locust embryogenesis. Hemocyanin presented a prominent expression in the revolution stage and exhibited strong responses to hypoxia. The relative duration of revolution was correlated negatively with the expression of hemocyanin subunit 2 (HC2), suggesting that HC2 might be closely associated with hypoxia adaptation of locust embryos. Furthermore, a HC2 mutant locust strain was established using the CRISPR/Cas9 technology, and higher hypoxia sensitivity was found for HC2-deficient locust embryos. Knockdown of HC2 increased anaerobic metabolism and oxidative stress while reducing oxidative metabolism. Overall, these findings clearly demonstrated the pivotal roles of hemocyanin in hypoxia adaptation of insect embryos.
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.