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吻肽驱动食用蛙(Pelophylax esculentus)的生殖细胞发育:一项体外睾丸实验研究

Kisspeptin drives germ cell progression in the anuran amphibian Pelophylax esculentus: a study carried out in ex vivo testes.

作者信息

Chianese Rosanna, Ciaramella Vincenza, Fasano Silvia, Pierantoni Riccardo, Meccariello Rosaria

机构信息

Dipartimento di Medicina Sperimentale Sezione "F. Bottazzi", Seconda Università di Napoli, Via Costantinopoli 16, 80138 Napoli, Italy.

Dipartimento di Scienze Motorie e del Benessere, Università di Napoli Parthenope, Via Medina 40, 80133 Napoli, Italy.

出版信息

Gen Comp Endocrinol. 2015 Jan 15;211:81-91. doi: 10.1016/j.ygcen.2014.11.008. Epub 2014 Nov 18.

Abstract

Kisspeptin, via Gpr54 receptor, regulates puberty onset in most vertebrates. Thus, the direct involvement of kisspeptin activity in testis physiology was investigated in the anuran amphibian, Pelophylax esculentus. In this vertebrate gpr54 mRNA has been localized in both interstitial compartment and spermatogonia (SPG), whereas SPG proliferation requires the cooperation between estradiol and testicular Gonadotropin releasing hormone (Gnrh). In the pre-reproductive period, dose response curve to assess the effects of Kisspeptin-10 (Kp-10) was carried out in vitro (dose range: 10(-9)-10(-6)M; incubation times: 1 and 4h); proliferative activity and germ cell progression were evaluated by expression analysis of proliferating cell nuclear antigen (pcna), estrogen receptor beta (erβ), Gnrh system (gnrh1, gnrh2, gnrhr1, r2, r3) and by the count of empty, mitotic and meiotic tubules. All selected markers were up regulated at 4h Kp-10 incubation. Histological analysis also proved the increase of mitotic activity and the progression of spermatogenesis. Besides Kp-10 modulation of testicular Gnrh system, in vitro treatment with 17β-estradiol (10(-6)M) ± the antagonist ICI182-780 (10(-5)M) revealed gnrh2 and gnrhr3 estrogen dependent expression. In the reproductive period, testes were incubated for 1 and 4h with Kp-10 (10(-7)M) or Kp-10 (10(-7)M)+kisspeptin antagonist [Kp-234 (10(-6)M)]. Results obtained in the pre-reproductive period were confirmed and Kp-234 completely counteracted Kp-10 effects. In conclusion, Kp-10 modulated the expression of pcna, erβ, gnrhs and gnrhrs, inducing the progression of the spermatogenesis.

摘要

亲吻素通过Gpr54受体调节大多数脊椎动物的青春期启动。因此,在无尾两栖动物食用蛙(Pelophylax esculentus)中研究了亲吻素活性在睾丸生理学中的直接作用。在这种脊椎动物中,gpr54 mRNA已定位在间质区室和精原细胞(SPG)中,而SPG增殖需要雌二醇和睾丸促性腺激素释放激素(Gnrh)之间的协同作用。在生殖前期,进行体外剂量反应曲线以评估亲吻素-10(Kp-10)的作用(剂量范围:10(-9)-10(-6)M;孵育时间:1和4小时);通过增殖细胞核抗原(pcna)、雌激素受体β(erβ)、Gnrh系统(gnrh1、gnrh2、gnrhr1、r2、r3)的表达分析以及空的、有丝分裂和减数分裂小管的计数来评估增殖活性和生殖细胞进展。所有选定的标志物在Kp-10孵育4小时时均上调。组织学分析也证明了有丝分裂活性的增加和精子发生的进展。除了Kp-10对睾丸Gnrh系统的调节外,用17β-雌二醇(10(-6)M)±拮抗剂ICI182-780(10(-5)M)进行体外处理显示gnrh2和gnrhr3的雌激素依赖性表达。在生殖期,将睾丸与Kp-10(10(-7)M)或Kp-10(10(-7)M)+亲吻素拮抗剂[Kp-234(10(-6)M)]孵育1和4小时。在生殖前期获得的结果得到证实,并且Kp-234完全抵消了Kp-10的作用。总之,Kp-10调节了pcna、erβ、gnrhs和gnrhrs的表达,诱导了精子发生的进展。

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