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帚尾袋貂(Trichosurus vulpecula)中的催乳素:利用重组帚尾袋貂催乳素开发同源放射免疫分析法。

Prolactin in the brushtail possum (Trichosurus vulpecula): development of homologous radioimmunoassay using recombinant possum prolactin.

作者信息

Crawford J L, Lun S, Demmer J, Eckery D C

机构信息

Reproduction Group, AgResearch Ltd., Wallaceville Animal Research Centre, Upper Hutt, New Zealand.

出版信息

Gen Comp Endocrinol. 2005 Jul;142(3):297-307. doi: 10.1016/j.ygcen.2005.02.001.

Abstract

We report the production of recombinant possum prolactin (posPrl), and its use in the development and validation of a highly specific homologous radioimmunoassay for the measurement of prolactin (Prl) in brushtail possums. This enabled the subsequent investigation of some basic mechanisms involved in the regulation of Prl secretion in this species. Recombinant posPrl spanning the entire coding region was expressed in Escherichia coli, resulting in a 199 amino acid protein with a molecular weight approximately 23 kDa. The potency of posPrl was 45.3 +/- 4.8% that of ovine Prl in a radioreceptor assay using possum mammary gland receptors and induced a 3.4 +/- 0.8-fold increase in progesterone secretion in primary possum granulosa cells. Antiserum (G27) was raised against recombinant posPrl and was highly specific for possum Prl (approximately 30% binding at 1:60,000 final dilution), and exhibited negligible cross-reactivity (<0.0001%) with possum growth hormone. Serial dilutions of pituitary gland extracts, and plasma samples from male and female possums gave parallel inhibition curves to recombinant posPrl standards in the assay. Biological validation of the RIA included treating possums with drugs known to alter Prl secretion in other mammals. In seasonally anoestrous female possums, administration of 20 microg thyrotropin-releasing hormone (TRH) resulted in a 15-fold increase (P < 0.01) in plasma Prl concentrations. In mid-late lactating female possums, a bolus of cabergoline (dopamine agonist; 75 microg) reduced (P < 0.05) plasma Prl levels to baseline for 24 h, while repeated administration (6 x 75 microg at 12 h intervals) suppressed (P < 0.01) plasma Prl concentrations until 24h after the last injection. Prolonged inhibition of Prl levels subsequently caused marked (P < 0.01) attenuation in rate of bodyweight increase of pouch young. The amplitude of the Prl surge in response to a bolus of TRH (15 microg) was 5-fold lower in cabergoline-treated, compared to control mid-late lactating possums. In conclusion, we report the development and validation of a robust and sensitive RIA for measuring Prl concentrations in the plasma of brushtail possums.

摘要

我们报道了重组负鼠催乳素(posPrl)的制备及其在开发和验证用于测量帚尾负鼠催乳素(Prl)的高特异性同源放射免疫分析中的应用。这使得后续能够研究该物种中Prl分泌调节所涉及的一些基本机制。跨越整个编码区的重组posPrl在大肠杆菌中表达,产生了一种199个氨基酸的蛋白质,分子量约为23 kDa。在使用负鼠乳腺受体的放射受体分析中,posPrl的效力为绵羊Prl的45.3±4.8%,并在原代负鼠颗粒细胞中诱导孕酮分泌增加3.4±0.8倍。针对重组posPrl制备了抗血清(G27),其对负鼠Prl具有高度特异性(在最终稀释度为1:60,000时约30%结合),并且与负鼠生长激素的交叉反应可忽略不计(<0.0001%)。垂体提取物以及雄性和雌性负鼠的血浆样品的系列稀释液在该分析中对重组posPrl标准品给出了平行抑制曲线。该放射免疫分析的生物学验证包括用已知可改变其他哺乳动物Prl分泌的药物处理负鼠。在季节性乏情的雌性负鼠中,给予20μg促甲状腺激素释放激素(TRH)导致血浆Prl浓度增加15倍(P<0.01)。在泌乳中后期的雌性负鼠中,注射一针卡麦角林(多巴胺激动剂;75μg)使血浆Prl水平在24小时内降至基线(P<0.05),而重复给药(每隔12小时6×75μg)可抑制(P<0.01)血浆Prl浓度直至最后一次注射后24小时。随后对Prl水平的长期抑制导致育儿袋幼崽体重增加率显著降低(P<0.01)。与对照泌乳中后期负鼠相比,卡麦角林处理的负鼠对一针TRH(15μg)反应的Prl激增幅度低5倍。总之,我们报道了一种用于测量帚尾负鼠血浆中Prl浓度的可靠且灵敏的放射免疫分析的开发和验证。

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