Pomatto Laura C D, Wong Sarah, Tower John, Davies Kelvin J A
Leonard Davis School of Gerontology of the Ethel Percy Andrus Gerontology Center, The University of Southern California, Los Angeles, CA 00089-0191, USA.
Leonard Davis School of Gerontology of the Ethel Percy Andrus Gerontology Center, The University of Southern California, Los Angeles, CA 00089-0191, USA,; Molecular and Computational Biology Program of the Department of Biological Sciences, Dornsife College of Letters, Arts, and Sciences, The University of Southern California, Los Angeles, CA 90089-0191, USA.
Arch Biochem Biophys. 2017 Dec 15;636:57-70. doi: 10.1016/j.abb.2017.10.021. Epub 2017 Oct 31.
Sexual dimorphism includes the physical and reproductive differences between the sexes, including differences that are conserved across species, ranging from the common fruit fly, Drosophila melanogaster, to humans. Sex-dependent variations in adaptive homeostasis, and adaptive stress responses may offer insight into the underlying mechanisms for male and female survival differences and into differences in chronic disease incidence and severity in humans. Earlier work showed sex-specific differences in adaptive responses to oxidative stressors in hybrid laboratory strains of D. melanogaster. The present study explored whether this phenomenon is also observed in wild-type D. melanogaster strains Oregon-R (Or-R) and Canton-S (Ca-S), as well as the common mutant reference strain w[1118], in order to better understand whether such findings are descriptive of D. melanogaster in general. Flies of each strain were pretreated with non-damaging, adaptive concentrations of hydrogen peroxide (HO) or of different redox cycling agents (paraquat, DMNQ, or menadione). Adaptive homeostasis, and changes in the expression of the Proteasome and overall cellular proteasomal proteolytic capacity were assessed. Redox cycling agents exhibited a male-specific adaptive response, whereas HO exposure provoked female-specific adaptation. These findings demonstrate that different oxidants can elicit sexually dimorphic adaptive homeostatic responses in multiple fly strains. These results (and those contained in a parallel study [1]) highlight the need to address sex as a biological variable in fundamental science, clinical research, and toxicology.
性二态性包括两性之间的生理和生殖差异,这些差异在从普通果蝇(黑腹果蝇)到人类等物种中都是保守的。适应性内稳态和适应性应激反应中的性别依赖性差异,可能有助于深入了解男性和女性生存差异的潜在机制,以及人类慢性疾病发病率和严重程度的差异。早期的研究表明,在黑腹果蝇的杂交实验室品系中,对氧化应激源的适应性反应存在性别特异性差异。本研究探讨了在野生型黑腹果蝇品系俄勒冈-R(Or-R)和广东-S(Ca-S)以及常见的突变参考品系w[1118]中是否也观察到这种现象,以便更好地理解这些发现是否总体上描述了黑腹果蝇的情况。对每个品系的果蝇用无损伤的、适应性浓度的过氧化氢(HO)或不同的氧化还原循环剂(百草枯、DMNQ或甲萘醌)进行预处理。评估了适应性内稳态、蛋白酶体表达的变化以及整体细胞蛋白酶体的蛋白水解能力。氧化还原循环剂表现出雄性特异性的适应性反应,而过氧化氢暴露则引发雌性特异性的适应。这些发现表明,不同的氧化剂可以在多个果蝇品系中引发性别二态性的适应性内稳态反应。这些结果(以及一项平行研究[1]中的结果)强调了在基础科学、临床研究和毒理学中将性别作为一个生物学变量加以考虑的必要性。