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Expression profiling of lipocalin-2 and 24p3 receptor in murine gonads at different developmental stages

机译:脂质运载蛋白-2和24p3受体在不同发育阶段的小鼠性腺中的表达谱

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摘要

Numerous clinical studies have reported the association between high circulating levels of lipocalin-2 (LCN2) and metabolic diseases. However, only few studies have addressed sexually dimorphic, either in its circulating concentration or in its expression in other organs. To the best of our knowledge, LCN2 and the 24p3 receptor (24p3R), have not been identified in gonads; therefore, the present study analyzed their mRNA expression profile and cellular localization in gonads collected from fetal rats at 21 days post coitum, as well as from neonatal rats at 0, 2, 4, 6, 12, 20 and 30 postnatal days. Semiquantitative polymerase chain reaction and immunohistochemical assays revealed that the LCN2 mRNA during perinatal and pre-pubertal stages presented a sex-specific expression pattern, being higher in ovaries than in testes collected at these stages. Furthermore, the mRNA levels of the long and short isoforms of the 24p3R (507 and 350 bp, respectively), were lower in female gonads from postnatal day 0 onwards in comparison with the levels observed in males, but before birth, the short isoform of the 24p3R was higher in ovaries than in testes. In addition, in females, the abundance of mRNA of this isoform was drastically diminished at 24 h after birth. Furthermore, this specific expression profile of LCN2 and 24p3R at perinatal and prepubertal stages coincides with events of cellular proliferation and apoptosis within both gonads. Immunohistochemical assays revealed that in ovaries, LCN2 and 24p3R are present in germinal and somatic cells of follicles, while in testes, this adipokine and its receptor are only located in germinal cells. These findings suggest that in murine gonads, LCN2/24p3R signaling may be involved either in cell proliferation or cell death driven by gonadotropin-independent or -dependent mechanisms.
机译:许多临床研究已经报告了脂环蛋白2(LCN2)的高循环水平与代谢性疾病之间的关联。但是,很少有研究针对性二态性,无论是其循环浓度还是在其他器官中的表达。据我们所知,尚未在性腺中鉴定出LCN2和24p3受体(24p3R)。因此,本研究分析了它们的mRNA表达谱和细胞在性交后21天收集的胎儿大鼠以及出生后0、2、4、6、12、20和30天新生大鼠的性腺中的细胞定位。半定量聚合酶链反应和免疫组化分析显示,围产期和青春期前的LCN2 mRNA表现出性别特异性表达模式,在卵巢中高于在这些阶段收集的睾丸中。此外,从出生后第0天开始,雌性腺中24p3R的长和短同工型的mRNA水平(分别为507和350 bp)低于男性,但在出生前,其同工型的短同工型的mRNA水平较低。卵巢中的24p3R高于睾丸。另外,在女性中,这种亚型的mRNA丰度在出生后24小时急剧下降。此外,LCN2和24p3R在围产期和青春期前的这种特异性表达谱与两个性腺中的细胞增殖和凋亡事件相吻合。免疫组织化学分析表明,卵巢中LCN2和24p3R存在于卵泡的生发和体细胞中,而在睾丸中,该脂肪因子及其受体仅位于生发细胞中。这些发现表明在鼠性腺中,LCN2 / 24p3R信号传导可能与促性腺激素非依赖性或依赖性机制驱动的细胞增殖或细胞死亡有关。

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