Departamentul de Tehnologii Apicole şi Sericicole, Universitatea de Ştiinţe Agricole şi Medicină Veterinară, 400372 Cluj-Napoca, Romania.
Departamentul de Tehnologii Apicole şi Sericicole, Universitatea de Ştiinţe Agricole şi Medicină Veterinară, 400372 Cluj-Napoca, Romania. Institut für Biologie, Molekulare Ökologie, Martin-Luther-Universität Halle-Wittenberg, 06099 Halle (Saale), Germany.
J Gerontol A Biol Sci Med Sci. 2014 Jun;69(6):633-9. doi: 10.1093/gerona/glt134. Epub 2013 Sep 27.
To date five different theories compete in explaining the biological mechanisms of senescence or ageing in invertebrates. Physiological, genetical, and environmental mechanisms form the image of ageing in individuals and groups. Social insects, especially the honeybee Apis mellifera, present exceptional model systems to study developmentally related ageing. The extremely high phenotypic plasticity for life expectancy resulting from the female caste system provides a most useful system to study open questions with respect to ageing. Here, we used long-lived winter worker honeybees and measured transcriptional changes of 14 antioxidative enzyme, immunity, and ageing-related (insulin/insulin-like growth factor signaling pathway) genes at two time points during hibernation. Additionally, worker bees were challenged with a bacterial infection to test ageing- and infection-associated immunity changes. Gene expression levels for each group of target genes revealed that ageing had a much higher impact than the bacterial challenge, notably for immunity-related genes. Antimicrobial peptide and antioxidative enzyme genes were significantly upregulated in aged worker honeybees independent of bacterial infections. The known ageing markers vitellogenin and IlP-1 were opposed regulated with decreasing vitellogenin levels during ageing. The increased antioxidative enzyme and antimicrobial peptide gene expression may contribute to a retardation of senescence in long-lived hibernating worker honeybees.
迄今为止,有五种不同的理论竞相解释无脊椎动物衰老或老化的生物学机制。生理、遗传和环境机制构成了个体和群体衰老的形象。社会性昆虫,尤其是蜜蜂(Apis mellifera),为研究与发育相关的衰老提供了特殊的模型系统。由于雌性等级制度导致的预期寿命极高的表型可塑性,为研究与衰老相关的开放性问题提供了一个非常有用的系统。在这里,我们使用了长寿的冬季工蜂,并在冬眠期间的两个时间点测量了 14 种抗氧化酶、免疫和与衰老相关(胰岛素/胰岛素样生长因子信号通路)基因的转录变化。此外,工蜂还受到细菌感染的挑战,以测试与衰老和感染相关的免疫变化。每个靶基因组的基因表达水平表明,衰老的影响比细菌感染大得多,特别是对与免疫相关的基因。抗菌肽和抗氧化酶基因在年老的工蜂中显著上调,而与细菌感染无关。已知的衰老标志物卵黄蛋白原和 IlP-1 的水平随着衰老而降低。抗氧化酶和抗菌肽基因表达的增加可能有助于延缓长寿冬眠工蜂的衰老。