Mattar Dareen, Cheewasopit Warakorn, Samir Moafaq, Knight Philip G
D Mattar, School of Biological Sciences, University of Reading, Reading, United Kingdom of Great Britain and Northern Ireland.
W Cheewasopit, School of Biological Sciences, University of Reading, Reading, United Kingdom of Great Britain and Northern Ireland.
Reprod Fertil. 2023 Feb 1;4(1). doi: 10.1530/RAF-22-0088.
Kisspeptin, a hypothalamic neuropeptide encoded by the KISS1 gene, has a pivotal role in promoting GnRH secretion in mammals. Kisspeptin and its receptor (KISS1R) are also expressed in certain peripheral tissues including gonads, suggesting intra-gonadal roles. Such actions at the level of the bovine ovary have not been explored previously. The current aims were to determine whether KISS1 and its receptor (KISS1R) are expressed in the bovine ovary and whether kisspeptin or a kisspeptin antagonist can modulate ovarian steroid production by cultured ovarian cells. Granulosa (GC) and theca interna (TC) were collected from antral follicles (3-18 mm) categorized into five class sizes. Early, mid and regressing corpora lutea (CL) were also collected for RT-qPCR analysis of KISS1 and KISS1R expression. Bovine TC and GC cultured under both non-luteinizing (serum-free) and luteinizing (serum-supplemented) conditions were treated for 4 days with kisspeptin-10 (10-10-10-6M) or kisspeptin antagonist (p234; 10-10-10-6M), alone and in combination with either FSH (GC), LH (TC) or forskolin (luteinized GC/TC). Steroid secretion (GC: oestradiol, progesterone; TC: androstenedione, progesterone; luteinized GC/TC: progesterone) was measured by ELISA and viable cell number determined by neutral red uptake assay. KISS1 and KISS1R transcripts were detected in TC, GC and CL with significant differences between follicle categories and CL stages. However, neither kisspeptin-10 nor kisspeptin antagonist affected steroid secretion or viable cell number in any of the four ovarian cell culture models. As such, the hypothesis that kisspeptin has a direct intra-ovarian role to modulate follicular or luteal steroidogenesis, or cell proliferation/survival, is not supported.
亲吻素是一种由KISS1基因编码的下丘脑神经肽,在促进哺乳动物促性腺激素释放激素(GnRH)分泌方面起着关键作用。亲吻素及其受体(KISS1R)也在包括性腺在内的某些外周组织中表达,提示其在性腺内发挥作用。此前尚未对牛卵巢水平上的此类作用进行过探索。当前的目的是确定KISS1及其受体(KISS1R)是否在牛卵巢中表达,以及亲吻素或亲吻素拮抗剂是否能调节培养的卵巢细胞的类固醇生成。从分为五类大小的有腔卵泡(3 - 18毫米)中收集颗粒细胞(GC)和内膜细胞(TC)。还收集了早期、中期和退化期的黄体(CL),用于对KISS1和KISS1R表达进行逆转录定量聚合酶链反应(RT - qPCR)分析。在非促黄体生成(无血清)和促黄体生成(补充血清)条件下培养的牛TC和GC,分别单独以及与促卵泡生成素(FSH,用于GC)、促黄体生成素(LH,用于TC)或福斯高林(用于黄体化的GC/TC)联合使用亲吻素 - 10(10 - 10 - 10 - 6M)或亲吻素拮抗剂(p234;10 - 10 - 10 - 6M)处理4天。通过酶联免疫吸附测定(ELISA)测量类固醇分泌(GC:雌二醇、孕酮;TC:雄烯二酮、孕酮;黄体化的GC/TC:孕酮),并通过中性红摄取试验确定活细胞数量。在TC、GC和CL中检测到KISS1和KISS1R转录本,卵泡类别和CL阶段之间存在显著差异。然而,在四种卵巢细胞培养模型中的任何一种中,亲吻素 - 10和亲吻素拮抗剂均未影响类固醇分泌或活细胞数量。因此,亲吻素具有直接的卵巢内作用来调节卵泡或黄体类固醇生成或细胞增殖/存活这一假设未得到支持。