Rutigliano Heloisa M, Adams Betty M, Jablonka-Shariff Albina, Boime Irving, Adams Thomas E
Department of Animal ScienceUniversity of California, Davis, One Shields Avenue, Davis, California 95616, USADepartments of Developmental Biology and Obstetrics and GynecologyWashington University School of Medicine, Campus Box 8103, 660 South Euclid Avenue, Saint Louis, Missouri 63110, USADepartment of AnimalDairy and Veterinary Sciences, School of Veterinary Medicine, Utah State University, 4815 Old Main Hill, Logan, Utah 84322, USADepartment of Animal ScienceUniversity of California, Davis, One Shields Avenue, Davis, California 95616, USADepartments of Developmental Biology and Obstetrics and GynecologyWashington University School of Medicine, Campus Box 8103, 660 South Euclid Avenue, Saint Louis, Missouri 63110, USADepartment of AnimalDairy and Veterinary Sciences, School of Veterinary Medicine, Utah State University, 4815 Old Main Hill, Logan, Utah 84322, USA
Department of Animal ScienceUniversity of California, Davis, One Shields Avenue, Davis, California 95616, USADepartments of Developmental Biology and Obstetrics and GynecologyWashington University School of Medicine, Campus Box 8103, 660 South Euclid Avenue, Saint Louis, Missouri 63110, USADepartment of AnimalDairy and Veterinary Sciences, School of Veterinary Medicine, Utah State University, 4815 Old Main Hill, Logan, Utah 84322, USA.
Reproduction. 2014 Aug;148(2):129-36. doi: 10.1530/REP-14-0063. Epub 2014 May 7.
We examined the half-life and biological activity of two single-chain proteins that combined portions of ovine FSH and LH. We proposed the hypothesis that these chimeric proteins would display LH and FSH activities and would promote follicle maturation in ewes. Estrus activity was synchronized using progestogen-impregnated vaginal pessaries. To negate the impact of endogenous LH and FSH, animals received serum-containing antibodies against GNRH 1 day before pessary removal (PR). At PR sheep (five animals per group) received a single injection (10 IU/kg, i.v.) of either the ovine-based (oFcLcα) gonadotropin analog, an ovine-based analog containing oLHβ truncated at the carboxyl terminus (oFcL(ΔT)cα), or a human-based gonadotropin analog (hFcLcα). Control animals received a comparable amount of gonadotropin-free protein. Ovulation was induced 3 days after PR using human chorionic gonadotropin (1000 IU, i.v.). Ovaries were collected 11 days after PR. Neither estradiol (E2) or progesterone (P4) production, development of preovulatory follicles or corpora lutea (CL) were noted in control animals receiving gonadotropin-free protein. Significant increase in the synthesis of E2 and P4 was noted in sheep receiving the dually active gonadotropin analogs. The number of CLs present 11 days after PR was significantly increased in sheep receiving the chimeric glycoproteins compared with control animals. The magnitude of the secretory and ovarian responses did not differ between hFcLcα and oFcLcα or between oFcLcα and oFcL(ΔT)cα. Immunoactivity of LH and FSH was low in control animals, but was significantly elevated in sheep receiving the gonadotropin analogs. In conclusion, ovine-based gonadotropin analogs are functionally active in sheep and a single injection is adequate to induce the development of multiple ovulatory follicles.
我们研究了两种结合了部分绵羊促卵泡激素(FSH)和促黄体生成素(LH)的单链蛋白的半衰期和生物活性。我们提出了这样的假设,即这些嵌合蛋白将表现出LH和FSH活性,并能促进母羊卵泡成熟。使用含孕激素的阴道栓使发情活动同步。为了消除内源性LH和FSH的影响,在取出阴道栓(PR)前1天,给动物注射抗促性腺激素释放激素(GNRH)的含血清抗体。在PR时,绵羊(每组5只动物)静脉注射(10 IU/kg)一剂基于绵羊的(oFcLcα)促性腺激素类似物、一种基于绵羊的含羧基末端截短的oLHβ的类似物(oFcL(ΔT)cα)或一种基于人类的促性腺激素类似物(hFcLcα)。对照动物注射等量的不含促性腺激素的蛋白。在PR后3天,使用人绒毛膜促性腺激素(1000 IU,静脉注射)诱导排卵。在PR后11天收集卵巢。接受不含促性腺激素蛋白的对照动物中,未观察到雌二醇(E2)或孕酮(P4)的产生、排卵前卵泡或黄体(CL)的发育。在接受具有双重活性的促性腺激素类似物的绵羊中,E2和P4的合成显著增加。与对照动物相比,接受嵌合糖蛋白的绵羊在PR后11天出现的CL数量显著增加。hFcLcα和oFcLcα之间或oFcLcα和oFcL(ΔT)cα之间的分泌和卵巢反应程度没有差异。对照动物中LH和FSH的免疫活性较低,但在接受促性腺激素类似物的绵羊中显著升高。总之,基于绵羊的促性腺激素类似物在绵羊中具有功能活性,单次注射足以诱导多个排卵卵泡的发育。