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首页> 外文期刊>Reproductive Biology and Endocrinology >Biochemical isolation and purification of ovulation-inducing factor (OIF) in seminal plasma of llamas
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Biochemical isolation and purification of ovulation-inducing factor (OIF) in seminal plasma of llamas

机译:美洲驼精浆中排卵诱导因子(OIF)的生化分离与纯化

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Background The objective of the present study was to isolate and purify the protein fraction(s) of llama seminal plasma responsible for the ovulation-inducing effect of the ejaculate. Methods Semen collected from male llamas by artificial vagina was centrifuged and the seminal plasma was harvested and stored frozen. Seminal plasma was thawed and loaded onto a Type 1 macro-prep ceramic hydroxylapatite column and elution was carried out using a lineal gradient with 350 mM sodium phosphate. Three protein fractions were identified clearly (Fractions A, B, and C), where a prominent protein band with a mass of 14 kDa was identified in Fraction C. Fraction C was loaded into a sephacryl gel filtration column for further purification using fast protein liquid chromatography (FPLC). Isocratic elution resulted in 2 distinct protein fractions (Fractions C1 and C2). An in vivo bioassay (n = 10 to 11 llamas per group) was used to determine the ovarian effect of each fraction involving treatment with saline (negative control), whole seminal plasma (positive control), or seminal plasma Fractions A, B or C2. Ultrasonography was done to detect ovulation and CL formation, and blood samples were taken to measure plasma progesterone and LH concentrations. Results Ovulation and CL formation was detected in 0/10, 10/11, 0/10, 2/11, and 10/11 llamas treated with saline, whole seminal plasma, Fractions A, B and C2 respectively (P Conclusion Ovulation-inducing factor was isolated from llama seminal plasma as a 14 kDa protein molecule that elicits a preovulatory LH surge followed by ovulation and CL formation in llamas, suggesting an endocrine effect at the level of the hypothalamus (release of GnRH) or the pituitary (gonadotrophs).
机译:背景技术本研究的目的是分离和纯化负责精液诱导排卵的美洲驼精浆的蛋白质部分。方法将雄性美洲驼通过人工阴道收集的精液进行离心分离,收集精浆并冷冻保存。解冻精浆,并将其加载到1型大容量制备型陶瓷羟基磷灰石柱上,并使用线性梯度与350 mM磷酸钠进行洗脱。清晰地鉴定出三个蛋白质级分(组分A,B和C),其中在级分C中鉴定出质量为14 kDa的突出蛋白带。将级分C装入sephacryl凝胶过滤柱中,以便使用快速蛋白液进一步纯化色谱(FPLC)。等度洗脱得到2个不同的蛋白质部分(组分C1和C2)。使用体内生物测定法(每组n = 10到11个美洲驼)来确定涉及用盐水(阴性对照),整个精浆(阳性对照)或精浆A,B或C2部分治疗的每个组分的卵巢效应。进行超声检查以检测排卵和CL的形成,并采集血样以测量血浆孕酮和LH浓度。结果在分别用生理盐水,全精浆,A,B和C2级分处理的骆驼中,分别在0 / 10、10 / 11、0 / 10、2 / 11和10/11美洲驼中检测到排卵和CL形成(P结论排卵诱导该因子是从美洲驼精浆中分离出来的一种14 kDa蛋白分子,引起排卵前LH激增,随后在美洲驼中排卵和CL形成,提示在下丘脑(GnRH的释放)或垂体(性腺营养不足)水平具有内分泌作用。

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