Department of Veterinary Biomedical Sciences, University of Saskatchewan, Saskatoon, Canada.
Reprod Biol Endocrinol. 2011 Feb 10;9:24. doi: 10.1186/1477-7827-9-24.
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.
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.
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<0.001). A surge in circulating concentrations of LH was detected within 2 hours only in llamas treated with either whole seminal plasma or Fraction C2. Plasma progesterone concentration and CL diameter profiles were greatest (P<0.05) in llamas treated with Fraction C2.
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).
本研究的目的是分离和纯化引起精液排卵作用的羊驼精液蛋白成分。
通过人工阴道从雄性羊驼中收集精液,离心,收集精液并冷冻储存。解冻精液并加载到 Type 1 宏制备陶瓷羟磷灰石柱上,使用 350 mM 磷酸钠线性梯度洗脱。清楚地鉴定出 3 种蛋白质级分(级分 A、B 和 C),其中级分 C 中鉴定出质量为 14 kDa 的突出蛋白带。级分 C 加载到 sephacryl 凝胶过滤柱中,使用快速蛋白质液相色谱(FPLC)进一步纯化。等度洗脱导致 2 种不同的蛋白质级分(级分 C1 和 C2)。体内生物测定(每组 10 至 11 只羊驼)用于确定每个级分的卵巢作用,涉及用盐水(阴性对照)、整个精液(阳性对照)或精液级分 A、B 或 C2 处理。进行超声检查以检测排卵和 CL 形成,并采集血液样本以测量血浆孕酮和 LH 浓度。
盐水、全精液、级分 A、B 和 C2 处理的 10/11、0/10、10/11、0/10 和 2/11 只羊驼分别检测到排卵和 CL 形成(P<0.001)。只有在用全精液或 C2 级分处理的羊驼中,才能在 2 小时内检测到循环 LH 浓度的激增。用 C2 级分处理的羊驼的血浆孕酮浓度和 CL 直径曲线最大(P<0.05)。
从羊驼精液中分离出排卵诱导因子,作为 14 kDa 蛋白分子,在羊驼中引发促黄体生成素前排卵激增,随后排卵和 CL 形成,表明在下丘脑(释放 GnRH)或垂体(促性腺激素)水平存在内分泌作用。